3505 Oncology Jobs - Page 2

*The Chittaranjan National Cancer Institute (CNCI), funded by the Government of India and the Government of West Bengal, was created in 1987 as a Regional Cancer Centre with the objective of developing it into an advanced institute catering to treatment, training, education and research in oncology,* *Job Opportunity: BSc Nursing Staff* Chittaranjan National Cancer Institute, located at DJ Block (Newtown), Action Area I, Newtown, Koch Pukur, West Bengal 700107, is inviting applications for the position of BSc Nursing Staff. *Job Details:* - *Designation:* BSc Nursing Staff - *Qualification:* BSc Nursing with 1 year of experience (mandatory) - *Age:* 21 to 35 years (Female candidates only) - *Duty Hours:* 8 hours - *Working Days:* 26 days - *Salary:* ₹30,000/- in-hand + PF + Medical + PL + CL + Yearly Bonus - *Job Type:* Central Government Contractual Job (up to 60 years) *Interested candidates can apply for this opportunity.* We are seeking experienced BSc Nursing professionals to join our team at Chittaranjan National Cancer Institute. This is a contractual job opportunity with the Central Government, with a job tenure up to 60 years. *Key Details:* - Qualification: BSc Nursing with 1 year of experience - Age: 21-35 years (Female candidates only) - Salary: ₹30,000/- + benefits - Job Type: Central Government Contractual Job *Don't miss this opportunity to join our team!* Nurse Job Description Job Summary We are seeking a compassionate and dedicated Nurse to join our healthcare team. The ideal candidate will be responsible for providing high-quality patient care, conducting clinical research, and offering clinical counseling. This role requires a strong understanding of medical terminology and the ability to engage in various therapeutic practices, including cognitive behavioral therapy and group therapy. The Nurse will work closely with patients to support their mental and physical health needs, particularly in outpatient settings and child family counseling. Responsibilities Deliver exceptional patient care by assessing individual needs and developing personalized care plans. Conduct clinical research to evaluate treatment effectiveness and improve patient outcomes. Provide clinical counseling to patients, utilizing techniques such as cognitive behavioral therapy and group therapy. Collaborate with social workers and other healthcare professionals to ensure comprehensive care for patients. Maintain accurate medical records and documentation in accordance with healthcare regulations. Educate patients and their families about health management, treatment options, and wellness strategies. Monitor patient progress and adjust care plans as necessary based on ongoing assessments. Engage in continuous professional development to stay current with best practices in nursing. Experience Previous experience in patient care is preferred, with a focus on outpatient services or child family counseling being advantageous. Familiarity with clinical research methodologies is a plus. Strong knowledge of medical terminology is essential for effective communication within the healthcare team. Experience in social work or related fields will be considered an asset. Ability to demonstrate empathy, patience, and strong interpersonal skills when interacting with patients. Join our team of dedicated professionals committed to making a difference in the lives of our patients through quality care and support. Job Type: Full-time Pay: ₹30,000.00 - ₹350,000.00 per month Schedule: Day shift Evening shift Night shift Work Location: In person

Company Description Jagannath Gupta Institute of Medical Sciences and Hospital (JIMSH), based in Budge Budge, Kolkata, has been a leading multi-specialty hospital and medical college since 2016. JIMSH offers top-tier medical education with 200 MBBS seats and robust nursing and paramedical programs. We are committed to shaping healthcare's future through comprehensive education, patient-centric care, and innovative research. Our 1200+ bed facility provides advanced healthcare services in nephrology, oncology, cardiology, and more, supported by the latest technology. Our mission is to advance medical practice and education while honoring the sanctity of life, promoting research, and engaging with community health needs. Role Description The Hospital Operations Manager will oversee the daily operations of the hospital, ensuring efficient and effective service delivery. Key responsibilities include managing staff, implementing policies, overseeing patient care services, handling budgets, and ensuring regulatory compliance. This is a full-time, on-site role located in Kolkata. Qualifications Experience in healthcare management and hospital operations Skills in staff management, policy implementation, and patient care services Knowledge of budgeting, financial management, and regulatory compliance Strong organizational and communication skills Ability to lead and motivate a diverse team Master's degree in Healthcare Administration, Business Administration, or a related field is preferred Experience in a multi-specialty hospital environment is a plus

🩺 We’re Hiring! Join Us in Transforming Government Healthcare Access 📍 Goel Super Speciality Hospital – 300-Bed NABH & QCI Accredited Hospital, Lucknow We are looking to expand our CGHS (Central Government Health Scheme) Department and are hiring experienced professionals in the following roles: 🔹 CGHS Billing & Documentation Expert 🔹 CGHS Consultant / Advisor (Healthcare Policies & Empanelment) 🔹 PRO & Marketing Professionals (with CGHS/ECHS/TPA exposure) 🔹 Doctors & Specialists familiar with CGHS protocol 🔹 Field Executives for peripheral OPDs and camp coordination ✅ Prior experience with CGHS, ECHS, and Government Healthcare Schemes preferred ✅ Excellent communication, knowledge of documentation & liaisoning is a plus 👨‍⚕️ Join our dedicated team of 50+ doctors and 200+ staff offering advanced care in: – Cardiology, Oncology, Neurosurgery, Urology, Orthopedics, Pediatrics, Gynae, ICU, NICU, Cath Lab & more – With empanelment under Ayushman Bharat, CGHS, ECHS, CM Relief Fund, and 40+ TPAs 📞 Apply Now Call or WhatsApp: 9151014001 / 02 / 03 📧 Email your CV: goelsuperspeciality@gmail.com 🌐 Visit: www.goelhospital.com 📍 697, Anora Kala, Near Royal City, Ayodhya Road, Chinhat, Lucknow – 226028 📸 Instagram: instagram.com/goelsuperspeciality 📘 Facebook: facebook.com/goelsuperspecialityhospital 📹 YouTube: youtube.com/@goelhospital #HiringNow #CGHSJobs #HealthcareJobsLucknow #GoelHospital #MedicalCareers #HospitalJobs #JoinOurTeam #TPAJobs #PROHiring #CGHSHiring #HospitalMarketing #DoctorsRequired #LucknowJobs

Contact Mr Manoj Thenua WhatsApp 63986528 32 🟢 Hiring: Consultant Onco Surgeon (MCh/DNB) 📍 Location: Visakhapatnam, Andhra Pradesh 🏥 Hospital Type: Tertiary Care / Multispecialty Hospital 🕒 Employment Type: Full-Time / Consultant 💼 Experience Required: 0-5 years (Freshers with MCh/DNB may also apply) 🔷 About The Hospital A leading multispecialty healthcare facility in Visakhapatnam with state-of-the-art infrastructure, advanced oncology services, and a multidisciplinary team approach for cancer care. 🩺 Role & Responsibilities Perform surgical oncology procedures for both solid and soft tissue tumors as per standard protocols. Evaluate, diagnose, and manage cancer patients requiring surgical intervention. Work closely with Medical Oncology and Radiation Oncology teams for comprehensive patient management. Provide preoperative and postoperative care ensuring patient safety and quality outcomes. Participate in tumor board discussions and contribute to treatment planning. Maintain detailed medical records and adhere to hospital policies. ✅ Key Requirements Qualification: MCh (Surgical Oncology) / DNB (Surgical Oncology) from a recognized institution. Registration: Valid registration with MCI/NMC or State Medical Council. Skills: Excellent surgical skills, patient-centric approach, ability to work in a team environment. Experience: Preferred 1-3 years post MCh/DNB, but freshers with strong clinical exposure are encouraged to apply. 💰 Compensation & Benefits Attractive salary package (Negotiable based on experience) Performance-based incentives Accommodation support if required Opportunities for academic growth and research Skills: preoperative care,teamwork,compensation,cancer,skills,excellent surgical skills,oncology,patient management,surgical oncology,clinical exposure,ability to work in a team environment,patient-centric approach,dnb,postoperative care,registration,advanced,art,team collaboration,mch

Our Team Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main Responsibilities Works with a team of Medical regulatory writers with different levels of expertise, Develops medical expertise within Medical regulatory writing (on contents, methods, and processes). Ensures compliance with regulatory requirements from various regions (FDA, EU others) for activities supported. Coordinates and supports medical activities related to the maintenance of the marketing authorizations of Established and Generic products, in different therapeutic areas. Works in close collaboration with Global Medical Leads, Global Regulatory Affairs, Global Pharmacovigilance, and vendors Essential Job duties and responsibilities: 1) Responsible to provide a medical assessment with relevant and updated clinical evidence and monitoring the execution of strategic documents such as PBRERs, ACOs, DSURs, Clinical Overviews, Benefit-Risk assessments, Expert statements for MDD, Responses to Health Authority Queries, Ad-hoc literature analyses, and labeling documents for the corresponding therapeutic area or products or any other activities which are the core activities of GMLs. 2) Drafting the extended synopsis of studies in collaboration with RWE experts. He/she will be responsible for overseeing the execution of such plans by the respective operational units in compliance with SOP, GCP, and other regulations. 3) Writing of Key medical/clinical parts of Common Technical Documents (CTD) or Briefing packages (BP). 4) Reviewing and approving compassionate use of individual medical requests for use of Sanofi medicinal products for serious or life-threatening diseases for treatment outside of clinical trials. 5) Secure delivery of high-quality medical documents on time and in compliance with internal and external standards. 6) Collaborates effectively with stakeholders: global medical leads/ medical product leads, global regulatory affairs, medical regulatory writing global or local teams, pharmacovigilance teams, managed access program teams. People: 1) Maintain effective relationships with the end stakeholders (Medical, regulatory, pharmacovigilance community) within the allocated Global business unit and product – with an end objective to develop medical regulatory content as per requirement, 2) Interact effectively with stakeholders in medical and pharmacovigilance departments 3) Constantly assist the medical regulatory writing team in developing knowledge and sharing expertise Performance: 1) Secure deliverables (PBRER, ACO, SO, CSR, ID Cards, Investigator brochure, clinical evaluation report, briefing packages, medical section of CTA, CTD, SBRAs, MDD, HAQs or any other activities which are core activities for GMLs) are supported as per agreed timelines and quality Process: 1) Provide medical strategic insights & evaluation related to Sanofi’s portfolio. 2) Contribute to the management of the marketing authorization dossiers of the current related portfolio. 3) Act as an expert in the field of medical regulatory writing and maintain the regulatory requirement for countries, and teams supported. 4) Assist the assigned medical team in conducting comprehensive medical regulatory writing-needs analysis 5) Implement relevant elements of the medical regulatory plan and associated activities for the year identified for the region 6) Work with selected vendors when required within the region to deliver the required deliverables as per the defined process 7) Assist the head of scientific communications in designing an overall plan of action based on end-customers feedback & improving course content and delivery Stakeholders: 1) Work closely with medical teams in regions/areas to identify medical writing needs and assist in developing assigned deliverables 2) Liaise with the Medical department to ensure relevant & customized are delivered per expectation About You Experience: ≥5 years of experience supporting international pharmaceutical companies: medical affairs, clinical development, pharmacovigilance with experience in at least one of the therapeutic areas- cardiovascular, metabolism, diabetes and lipid, CNS, oncology, anti-infectives, internal medicine Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment Technical skills: As applicable (Including but not limited to Medical operational excellence, time, and risk management skills, Excellent technical (medical) editing and writing skills) Education: Medical degree MBBS; MD Languages: Excellent knowledge of the English language (spoken and written) Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! null Pursue Progress . Discover Extraordinary . Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Job Description / Capsule Mentors others, has regional impact beyond own geographical area of responsibility. Introduces best practices to peers. Consistently high performer. Job Location: Indore/Bhopal ( Entire Central India ) Product : Imfinzi Lung Typical Accountabilities Successfully complete all training requirements, including product examinations. Engage Oncology healthcare professionals in dialogue about approved indications and product efficacy/safety profiles to support on-label prescribing for appropriate patients. Work with Sales Manager to develop a local strategy and business plan to meet or exceed sales and call execution goals in territory Drive sales performance and ensure sales forecasts and assigned budgets meet or exceed therapeutic and territory expectations. Develop and maintain in-depth knowledge of market, demographic, and managed markets information relative to assigned sales territory. Comply with all regulations regarding interactions with healthcare professionals, distribution of samples, etc. Essential Bachelor’s degree 3 Years experience in Oncology Desirable MNC Oncology experience Currently handling Lung portfolio Why AstraZeneca? At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. Global Career Level D AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements Date Posted 01-Aug-2025 Closing Date 15-Aug-2025 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

As a Key Accounts Manager in the Oncology sector based in Indore/Bhopal, your primary responsibility will be to engage with oncology healthcare professionals and provide them with scientific information on approved indications, efficacy, and safety to facilitate appropriate on-label use. You will collaborate closely with the Sales Manager to develop and implement territory-specific strategies and business plans to exceed sales targets and call execution goals. To excel in this role, you must successfully complete all mandatory training programs and product certifications. Your role will also involve maintaining a comprehensive understanding of the market landscape, customer demographics, and managed care environment within your territory. It is crucial to deliver strong sales performance consistently, meeting or surpassing sales forecasts and budgets. The ideal candidate for this position should hold a Bachelor's degree, preferably in Science or Pharmacy, along with a minimum of 3 years of experience in Oncology sales. Desirable qualifications include prior experience with a multinational pharmaceutical company (MNC) and expertise in managing or working with the GUGYN (Gynecologic & Urologic Oncology) portfolio. Moreover, it is essential to adhere strictly to company policies and regulatory requirements, especially concerning interactions with healthcare professionals and sample distribution. Your role as a Key Accounts Manager will involve mentoring peers, introducing best practices, and driving high performance throughout the region.,

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function Medical Affairs Group Job Sub Function Medical Science Liaison Job Category Scientific/Technology All Job Posting Locations: Bangalore, Karnataka, India, Chennai, Tamil Nadu, India Job Description Job Description: Johnson & Johnson is recruiting for Medical Science Liaison– Oncology, Medical Affairs located in Bangalore, India. The position reports to the TA Lead – Oncology, Johnson & Johnson Innovative Medicine, India. Position Overview Be a therapeutic area scientific expert where you will be scientific face of the company engaging in interactions with Key Opinion Leaders(KOL) discussing treatment trends, clinical trial data of our molecules and seeking insights that support the medical strategy. Key Responsibilities Primary scientific face of the organization to KOL’s for Oncology therapy area, responsible for: Identification, mapping and profiling of KOL’s of the given geography and therapy area on an ongoing basis Engagement of identified KOL’s through medical affairs initiatives in alignment with the overall franchise plan Represent the TA for medical & scientific affairs on all relevant cross functional teams and internal and external initiatives. Gathering customer insights and conveying them back to the franchise team Receiving and processing scientific information request received from Healthcare Professionals(HCP) Scientific resource for the sales team of the given therapy area responsible for regular training and flow of latest medical developments in the given field This is a highly collaborative role that requires excellent communication and influencing skills with all internal stakeholders to develop and implement medical strategy, to shape the external scientific landscape that can enable the fastest access to new products/indications for our patients, medical staff and the greater community. The position will require 70-80% travel for interaction with customers and various stakeholders. Qualifications - External Medical graduate (MD/ MBBS/ BDS /MDS) or Pharmaceutical university Degree ( PharmD or PhD) Experience And Skills Minimum of 0-2 years’ experience in pharmaceutical/healthcare industry Good understanding of medical affairs function Understanding of local regulatory policy and industry's code of practice related to drug registration, pharmaceutical promotion and clinical research. Are you ready to impact the world? Johnson & Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

About Strand Life Sciences: Strand is a 24-year-old spin-off from the Indian Institute of Science. We are a cutting-edge Genomics company with a global customer base. We build applications that use DNA sequencing to improve human health. In the process, we build algorithms, data pipelines, and visualizations to handle large amounts of sequence data. We are committed to transforming complex data into actionable insights, contributing to groundbreaking research and innovative solutions in the field of genomics. We anticipate that in the next few years, hundreds of millions of individuals will have their DNA sequenced, and invite you to join us in this transformative journey. About the Position We are looking for scientists with a background in genetics, molecular biology, oncology or related areas .The role involves analyzing the data obtained from NGS sequencing of patient samples for biological and clinical relevance. The role is scientifically stimulating and curators will find themselves getting familiarized with various aspects of cancer biology, genomics, and cancer therapies. Job Requirements and Required Skills: ? Masters degree in Cell Biology, Genetics, Molecular Biology, Oncology, Immunology or a related field ? 1-2 years of experience in cancer genomics desirable ? Ability to read and comprehend scientific papers, critically assess results and summarize them. ? Careful attention to detail ? Strong writing and analytical skills ? Ability to follow standard operating procedures and work under deadlines We offer: ? An innovative and open culture in a truly multicultural environment ? An opportunity to make a fundamental impact on human health ? Vibrant multidisciplinary scientific interaction and learning opportunity ? A collaborative and solution-oriented environment where you can make a difference ? A competitive salary and generous benefits Show more Show less

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function Medical Affairs Group Job Sub Function Medical Science Liaison Job Category Scientific/Technology All Job Posting Locations: Bangalore, Karnataka, India, Chennai, Tamil Nadu, India Job Description Job Description: Johnson & Johnson is recruiting for Medical Science Liaison– Oncology, Medical Affairs located in Bangalore, India. The position reports to the TA Lead – Oncology, Johnson & Johnson Innovative Medicine, India. Position Overview Be a therapeutic area scientific expert where you will be scientific face of the company engaging in interactions with Key Opinion Leaders(KOL) discussing treatment trends, clinical trial data of our molecules and seeking insights that support the medical strategy. Key Responsibilities Primary scientific face of the organization to KOL’s for Oncology therapy area, responsible for: Identification, mapping and profiling of KOL’s of the given geography and therapy area on an ongoing basis Engagement of identified KOL’s through medical affairs initiatives in alignment with the overall franchise plan Represent the TA for medical & scientific affairs on all relevant cross functional teams and internal and external initiatives. Gathering customer insights and conveying them back to the franchise team Receiving and processing scientific information request received from Healthcare Professionals(HCP) Scientific resource for the sales team of the given therapy area responsible for regular training and flow of latest medical developments in the given field This is a highly collaborative role that requires excellent communication and influencing skills with all internal stakeholders to develop and implement medical strategy, to shape the external scientific landscape that can enable the fastest access to new products/indications for our patients, medical staff and the greater community. The position will require 70-80% travel for interaction with customers and various stakeholders. Qualifications - External Medical graduate (MD/ MBBS/ BDS /MDS) or Pharmaceutical university Degree ( PharmD or PhD) Experience And Skills Minimum of 0-2 years’ experience in pharmaceutical/healthcare industry Good understanding of medical affairs function Understanding of local regulatory policy and industry's code of practice related to drug registration, pharmaceutical promotion and clinical research. Are you ready to impact the world? Johnson & Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . Position Internal Audit Analyst III, Global Internal Audit & Assurance (EG 100) Location Hyderabad, India Reports To Associate Director, IT Audit At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. Across oncology, hematology, immunology, neuroscience, and cardiovascular disease, with one of the most diverse and promising pipelines in the industry, each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Summary The Internal Audit Analyst III in GIA will work in a team environment to plan and execute dynamic risk-based audits and identify value-added recommendations to strengthen Company processes and controls. Audits will include U.S.-based operations, international Company subsidiaries, strategic initiatives, critical business processes, and key third-party outsourcing arrangements. Throughout the audits, the Senior Internal Audit Analyst will have the opportunity to interact with senior management and enhance oral and written communication skills. Key Responsibilities Key responsibilities include, but are not limited to Work collaboratively with audit teams to execute financial, operational, compliance, and integrated-IT audits. Conduct planning activities to identify significant risks and develop appropriate risk-based audit procedures. Research applicable policies, guidance, and regulations to drive assigned sections of the audit with high quality and within deadlines. Leverage existing data analytics AI use cases and assist with build and enhancement projects, when assigned. Interview key personnel to assess business processes and the strength of their control environments. Identify meaningful value-added recommendations for management to improve the adequacy, effectiveness, and efficiency of controls and related processes. Lead meetings involving various levels of management to effectively communicate audit status, align on significant audit issues and recommended corrective actions. Prepare clear, detailed audit documentation evidencing the results of actual testing procedures in accordance with BMS and the Institute of Internal Auditors (IIA) standards. Prepare audit reports, including clearly written, concise audit observations that effectively communicate identified issues and their related corrective actions to key stakeholders. Participate with the team in trainings and regular departmental meetings that include sharing best practices. Participate in departmental projects as assigned (e.g., audit lessons learned, training, continuous improvement, etc.). Qualifications & Experience A BA/BS degree in Data Science, Computer Science, Information Systems, Accounting, Finance, or other business discipline. A minimum of 4 years prior public accounting or internal audit experience, including experience in financial, operational, IT or compliance auditing. Knowledge of U.S. GAAP and IIA standards. English fluency. Strong verbal and written communication skills. Proficiency with Excel/Word/PowerPoint. AI and Data analytics experience (specifically with visualization tools such as Tableau) and ERPs. Desirable Qualifications & Experience MBA or other advanced degree. Professional certification (i.e., CPA, CA, CIA, CISA or equivalent). Experience with a Big Four firm. Experience in developing written reports and delivering presentations. Multilingual (verbal and written). Key Capabilities of Focus Leadership Pursues tasks with a sense of urgency. Shows accountability by taking ownership of assigned responsibilities and completing them on time, with the highest quality. Demonstrates speed and innovation to get things done; can simplify complex processes; knows of and can leverage resources to drive tasks/projects forward across functions and within the function. Able to identify risk and quickly develop an understanding of complex processes. Works effectively in ambiguous situations and adapts quickly in a rapidly changing environment. Collaboration Works well in a team environment, fostering inclusion and building effective relationships with both team members and customers. Displays excellent ability to communicate across various levels of management, including with executives, to explain identified issues and related corrective actions. Digital Proficiency Actively works toward improving data analytics capabilities and developing digital acumen. Gathers relevant information and critically evaluates it to define next steps and propose a solution. Business Acumen This role requires strong and proven ability to understand local and micro business dynamics, identify risks and opportunities. Why You Should Apply Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. [Senior Manager Software Development Engineering] What You Will Do Let’s do this. Let’s change the world. In this vital role you will be responsible for designing, developing, and maintaining software applications and solutions that meet business needs and ensuring the availability and performance of critical systems and applications. This role involves working closely with product managers, designers, and other engineers to create high-quality, scalable software solutions and automating operations, monitoring system health, and responding to incidents to minimize downtime. Roles & Responsibilities: Provide technical leadership to enhance the culture of innovation, automation, and solving difficult scientific and business challenges. Technical leadership includes providing vision and direction to develop scalable reliable solutions. Provide leadership to select right-sized and appropriate tools and architectures based on requirements, data source format, and current technologies Develop, refactor, research and improve Weave cloud platform capabilities. Understand business drivers and technical needs so our cloud services seamlessly, automatically, and securely provides them the best service. Develop data flow pipelines to extract, transform, and load data from various data sources in various forms, including custom ETL pipelines that enable model and product development Build strong partnership with stakeholder Build data products and service processes which perform data transformation, metadata extraction, workload management and error processing management to ensure high quality data Provide clear documentation for delivered solutions and processes, integrating documentation Collaborate with business partners to understand user stories and ensure technical solution/build can deliver to those needs Work with multi-functional teams to design and document effective and efficient solutions. Develop change management strategies and assist in their implementation. Mentor junior data engineers on standard methodologies in the industry and in the Amgen data landscape What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Basic Qualifications and Experience: Doctorate Degree /Master's degree / Bachelor's degree and 12to 17 years Computer Science, IT or related field experience Preferred Skills: Must-Have Skills: Superb communication and interpersonal skills, with the ability to work cross-functionally with multi-functional GTM, product, and engineering teams. Minimum of 10+ years overall Software Engineer or Cloud Architect experience Minimum 3+ years in architecture role using public cloud solutions such as AWS Experience with AWS Technology stack Good-to-Have Skills: Familiarity with big data technologies, AI platforms, and cloud-based data solutions. Ability to work effectively across matrixed organizations and lead collaboration between data and AI teams. Passion for technology and customer success, particularly in driving innovative AI and data solutions. Experience working with teams of data scientists, software engineers and business experts to drive insights Experience with AWS Services such as EC2, S3, Redshift/Spectrum, Glue, Athena, RDS, Lambda, and API gateway. Experience with Big Data Technologies (Hadoop, Hive, Hbase, Pig, Spark, etc) Good understanding of relevant data standards and industry trends Ability to understand new business requirements and prioritize them for delivery Experience working in biopharma/life sciences industry Proficient in one of the coding languages (Python, Java, Scala) Hands on experience writing SQL using any RDBMS (Redshift, Postgres, MySQL, Teradata, Oracle, etc.). Experience with Schema Design & Dimensional data modeling. Experience with software DevOps CI/CD tools, such Git, Jenkins, Linux, and Shell Script Hands on experience using Databricks/Jupyter or similar notebook environment. Experience working with GxP systems Experience working in an agile environment (i.e. user stories, iterative development, etc.) Experience working with test-driven development and software test automation Experience working in a Product environment Good overall understanding of business, manufacturing, and laboratory systems common in the pharmaceutical industry, as well as the integration of these systems through applicable standards. Soft Skills: Excellent analytical and troubleshooting skills. Ability to work effectively with global, virtual teams High degree of initiative and self-motivation. Ability to handle multiple priorities successfully. Team-oriented, with a focus on achieving team goals What You Can Expect Of Us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description We are seeking a visionary and decisive Program Manager to lead our Commercial Leadership Program in Hyderabad, India. As a key member of the team, you will be responsible for driving strategic initiatives to drive base portfolio profitability, lead end-to-end governance and action-tracking. You’ll ensure strategic alignment across multiple projects, rigorously monitor progress, and escalate issues when necessary. Reporting to the Head of B2B Excellence, you’ll collaborate with cross-functional teams (CFTs) in marketing, sales, regulatory, supply chain, sourcing, and finance. This role demands a blend of operational discipline, strategic foresight, and stakeholder management. Key Responsibilities Develop and maintain comprehensive program plans, overall savings committed, including timelines, milestones, and resource allocations. Implement and oversee governance frameworks that standardize decision-making, risk mitigation, and issue resolution. Drive action tracking by setting up dashboards, facilitating weekly review meetings, and ensuring accountability. Monitor program health using KPIs (e.g., on-time delivery, budget variance, risk index) and generate regular executive reports. Define contingency plans as per the plan and health indices. Cross-Functional Collaboration Act as the primary liaison between functional leads in CFT’s such as Regulatory Affairs, Supply Chain, and Sales. Coordinate with external vendors and partners, managing contracts and ensuring SLA adherence. Build strong relationships with senior stakeholders to surface roadblocks early and speed up decision cycles. Governance & Action Tracking Effective governance and action tracking empower timely decisions and course corrections. Defining governance cadence (e.g., steering committees, working group meetings) and RACI matrices. Tracking issue logs and risk registers, driving closure through structured follow-ups. Leading post-mortems to capture lessons learned and integrate process improvements. Qualifications 8-10+ years of experience in program management or related field Proven track record of leading cross-functional teams and developing talent Strong business acumen and understanding of commercial operations Excellent project management skills with ability to manage multiple initiatives simultaneously Advanced strategic planning and analytical capabilities Outstanding leadership, communication, and presentation skills Proficiency in data analysis and performance metrics Experience in stakeholder management and ability to influence at all levels of the organization Knowledge of industry trends and market dynamics Problem-solving and decision-making skills with a results-oriented mindset Experience working in or familiarity with the generic pharmaceutical industry is a must Project Management Professional (PMP) certification is a plus Additional Information Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com

Company Overview: We/eteraflex connects a fast-growing global CRO specializing in oncology, rare diseases, and immunotherapies. Our mission is to accelerate access to innovative treatments by combining regulatory precision with deep site engagement, particularly in complex government-led research environments across India. Position Summary: We are seeking an experienced Clinical Trial Manager (CTM) to lead the execution of Phase I, II and III oncology studies at key national institutions in India. This role is pivotal in driving site activation, regulatory compliance, and clinical delivery in alignment with global sponsor expectations. Key Responsibilities: Lead clinical operations and site-level engagement for assigned Phase’s studies in India Manage relationships with Principal Investigators (PIs), CRCs, and Institutional stakeholders at government hospitals Oversee timely and compliant PSSV, site initiation visits (SIV), patient recruitment, and data collection Ensure study milestones are met, including First Patient First Visit (FPFV) and clean database targets Collaborate with sponsor teams, regulatory consultants, and third-party vendors to streamline dossier submissions and audit readiness Coordinate regulatory submissions and ethics committee (EC) approvals; ensure alignment with CDSCO, ICMR, and local EC timelines Conduct ongoing risk assessment and drive mitigation strategies across sites Provide oversight to field CRAs and monitor site compliance Contribute to internal SOP development and quality initiatives Key Qualifications: Bachelor’s degree in life sciences or related field; advanced degree preferred Minimum 6-8 years of clinical research experience with at least 3 years in an independent CTM role Demonstrated experience in oncology or immunotherapy trials, preferably with exposure to AIIMS or government research centers Strong working knowledge of GCP, ICH, and CDSCO guidelines Proven track record managing multi-site studies and remote monitoring teams Excellent interpersonal, communication, and problem-solving skills Proficiency in CTMS, EDC, and eTMF systems is a plus Willingness to travel across India as needed (up to 25%)

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company’s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. Find out more about us at www.jubilantpharmova.com . The Position Organization- Jubilant Pharmova Limited Designation – Chemist Production Location- Nanjangud, Mysore Key Responsibilities. Intermediate/Clean room/SRP: Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents. To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents. Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected. To ensure that the respective equipment is calibrated Maintaining the respective equipment /Area in clean condition. Online updating of equipment status boards w.r.t to equipment status. Identifying /Labelling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated place. Identify the abnormalities associated risk and objectives by cross verifying the interlocks in equipment. To ensure the availability of utilities and to maintain the same by requesting utility department whenever required. Material Handling: Receiving the raw material from the stores and storage of raw materials in the designated place Identification and storage of intermediates/ API’s in the designated place. Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected. To maintain the accessories per respective SOP. Documentation: To indent, receive and issue therequired documents with in timeline according to pre-approved instructions. To ensure that documents being recorded contemporaneously. To ensure the records are updating contemporaneously and to facilitate the required documents. To ensure the availability of calibration documents where ever required. To ensure that those documents are completed and signed. To ensure the online entries of status board, log books and daily updating documents. To ensure the accessories are properly maintained/ destructed as per the respective SOP and it is properly documented. To submit the completed documents with in the timeline as per respective SOP Safety, health and environment: On line monitoring of the environment conditions in process area Person Profile . Qualification - Degree in Science / Graduate Engineers - Chemical/Diploma in Chemical Engineering (Chemistry/Chemical/PCM/Bio-Chemistry) Experience- 5-10 Years of relevant experience from API industry only Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company’s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. Find out more about us at www.jubilantpharmova.com . The Position Organization- Jubilant Pharmova Limited Designation – CProduction Location- Nanjangud, Mysore Key Responsibilities. Intermediate/Clean room/SRP: Producing Intermediates/API/Solvent Recovery according to pre-approved instructions and to record the same in respective BPR/documents. To perform the cleaning activity as per the procedure and to record the same in respective BCR/documents. Maintaining the Intermediate/Pharma/SRP and equipment clean and well appropriately disinfected. To ensure that the respective equipment is calibrated Maintaining the respective equipment /Area in clean condition. Online updating of equipment status boards w.r.t to equipment status. Identifying /Labelling of accessories (e.g. Scoop /Scrapper/Hose pipe/Filter bags/ AHU filters / micron filter cartridges) and storing the same in designated place. Identify the abnormalities associated risk and objectives by cross verifying the interlocks in equipment. To ensure the availability of utilities and to maintain the same by requesting utility department whenever required. Material Handling: Receiving the raw material from the stores and storage of raw materials in the designated place Identification and storage of intermediates/ API’s in the designated place. Maintaining the RM/ intermediate/ rejected material storage area clean and when appropriate disinfected. To maintain the accessories per respective SOP. Documentation: To indent, receive and issue therequired documents with in timeline according to pre-approved instructions. To ensure that documents being recorded contemporaneously. To ensure the records are updating contemporaneously and to facilitate the required documents. To ensure the availability of calibration documents where ever required. To ensure that those documents are completed and signed. To ensure the online entries of status board, log books and daily updating documents. To ensure the accessories are properly maintained/ destructed as per the respective SOP and it is properly documented. To submit the completed documents with in the timeline as per respective SOP Safety, health and environment: On line monitoring of the environment conditions in process area Person Profile . Qualification - Degree in Science / Graduate Engineers - Chemical/Diploma in Chemical Engineering (Chemistry/Chemical/PCM/Bio-Chemistry) Experience- 1 -10 Years of relevant experience from API industry only Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company’s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. Find out more about us at www.jubilantpharmova.com . The Position Organization- Jubilant Pharmova Limited Designation – Assistant Manager Engineering Location- Nanjangud, Mysore Key Responsibilities. Overall responsible for Mechanical Maintenance activities of Plant-5 & Plant-5 SRP Discussing with Plant Managers and getting clearance for Preventive, Breakdown & Corrective maintenance equipment in coordination of Civil, Electrical, HVAC and Instrumentation department Planning of spares for critical / Non critical equipment and initiate procurement action. Working with SAP-ERP system like handling Service requests, Work orders, Purchase requests, PM, Service entry, Reservations to withdraw materials, creating RGP/NRGP and GRN approvals etc Budget Preparation, monitoring and control. Initiate the relevant work permit to execute the jobs. SOP and On job training to subordinates. To Prepare, update and maintain documents like PM Checklist, SOP & Qualifications. Online Audit preparations & Facing audits. Tracking of pending notifications and work allotment for Asst. Foreman, Technician and Contractors Completion of notification / work order immediately after completion of jobs Verify the quality and quantity of work carried out by contractors & Certification of contractor invoices Preparation of engineering drawing for Eqpt. spares, local procurement, Import substitute Follow-up of fabrication job by visiting the Contactor shed area. Taking Plant round and ensure the work execution with good quality and Safety. Initiation and executing the Preventive maintenance of equipment in coordination of Production, Electrical and Instrumentation department. If any major abnormality observed during PM, plan for corrective actions & rectification. Filling the Major maintenance form / History card for the critical jobs completed in the plant. Preparation of material reconciliation sheet for the materials issued to contractors Preparation of RCA for breakdowns To implement energy saving initiatives across site Ensure and implement good Housekeeping, 5S and TPM initiatives. Any new item required, fill the Item Code Requisition form and take a follow-up with the Item code cell for new codes. Discussing with Plant Managers for CAPEX requirement & online initiation. Using compliance wire as a learning tool. Verification of the cage hoist and its interlocks on daily basis Handling deviations, Change management, review and approval through Track wise & EDMS Using compliance wire as a learning tool. Person Profile . Qualification - Diploma in Engineering/ Graduate Engineers Experience- 8+ Years Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, Please visit our LinkedIn Page- https://www.linkedin.com/company/jubilantpharmova/mycompany/

Do you want to make an impact on patient health around the world? Do you thrive in a fast-paced environment that brings together scientific, clinical, and commercial domains through engineering, data science, and analytics? Then join Pfizer Digital’s Artificial Intelligence, Data, and Advanced Analytics organization (AIDA) where you can leverage cutting-edge technology to inform critical business decisions and improve customer experiences for our patients and physicians. Our collection of engineering, data science, and analytics professionals are at the forefront of Pfizer’s transformation into a digitally driven organization that leverages data science and advanced analytics to change patients’ lives. The Data Science Industrialization team within Data Science Solutions and Initiatives leads the scaling of data and insights capabilities - critical drivers and enablers of Pfizer’s digital transformation. As the AI and Data Science Production Deployment Lead, you will be a leader within the Data Science Industrialization team charged with driving the deployment of AI use cases and reusable components into full production. You will lead a global team and partner with cross-functional business stakeholders and Digital leaders to catalyze identification, design, iterative development, and continuous improvements of deployment processes to support production data science workflows and AI applications. Your team will define and implement standard processes for quality assurance, testing, data ops, model ops, and dev ops while also providing SDLC, support, platform engineering, and cloud engineering guidance as needed. In addition, you will be responsible for providing critical input into the AI ecosystem and platform strategy to promote self-service, drive productization and collaboration, and foster innovation. Your team will be accountable to key Pfizer business functions (including Pfizer Biopharma, R&D, PGS, Oncology, and Enabling Functions) for production deployments of data science workflows and AI solutions that support major business objectives across all of Pfizer’s core business units. Role Responsibilities Lead deployment of production AI solutions and reusable software components with automated self-monitoring QA/QC processes Implement QA and testing, data ops, model ops, and DevOps for data science workflow products, industrialized workflow accelerators, and best practices in the production deployment of scalable AI/ML analytic insights products Enforce best practices for QA and testing and SDLC production support to ensure reliability and availability of deployed software Act as a subject matter expert for production deployment processes of data science workflows, AI solutions, and reusable software components on cross functional teams in bespoke organizational initiatives by providing thought leadership and execution support Direct QA and testing, data ops and model ops, DevOps, platform and cloud engineering research, advance data science workflow CI/CD orchestration capabilities, drive improvements in automation and self-service production deployment processes, implement best practices, and contribute to the broader talent building framework by facilitating related trainings Set a vision, prioritize workstreams, and provide day-to-day leadership, supervision, and mentorship for a global team with technical & functional expertise that includes QA and testing, DevOps, data science, and operations Coach direct reports to adopt best practices, improve technical skills, develop an innovative mindset, and achieve professional growth through technical and organizational thought leadership Communicate value delivered through reusable AI components to end user functions (e.g., Chief Marketing Office, Biopharma Commercial and Medical Affairs) and evangelize innovative ideas of reusable & scalable development approaches/frameworks/methodologies to enable new ways of developing and deploying AI solutions Partner with other leaders within the Data Science Industrialization team to define team roadmap and drive impact by providing strategic and technical input including platform evolution, vendor scan, and new capability development Partner with AI use case development teams to ensure successful integration of reusable components into production AI solutions Partner with AIDA Platforms team on end to end capability integration between enterprise platforms and internally developed reusable component accelerators (API registry, ML library / workflow management, enterprise connectors) Partner with AIDA Platforms team to define best practices for production deployment of reusable components to identify and mitigate potential risks related to component performance, security, responsible AI, and resource utilization Basic Qualifications Bachelor’s degree in AI, data science, or engineering related area (Computer Engineering, Computer Science, Information Systems, Engineering or a related discipline) 10+ years of work experience in data science, or engineering, or operations for a diverse range of projects 2-3 years of hands-on experience leading data science or AI/ML deployment and operations teams Track record of managing stakeholder groups and effecting change Recognized by peers as an expert in production deployment and AI/ML ops with deep expertise in CI/CD and DevOps for monitoring and orchestration of data science workflows, and hands-on development Understands how to synthesize facts and information from varied data sources, both new and pre-existing, into clear insights and perspectives that can be understood by business stakeholders Clearly articulates expectations, capabilities, and action plans; actively listens with others’ frame of reference in mind; appropriately shares information with team; favorably influences people without direct authority Clearly articulates scope and deliverables of projects; breaks complex initiatives into detailed component parts and sequences actions appropriately; develops action plans and monitors progress independently; designs success criteria and uses them to track outcomes; engages with stakeholders throughout to ensure buy-in Manages projects with and through others; shares responsibility and credit; develops self and others through teamwork; comfortable providing guidance and sharing expertise with others to help them develop their skills and perform at their best; helps others take appropriate risks; communicates frequently with team members earning respect and trust of the team Experience in translating business priorities and vision into product/platform thinking, set clear directives to a group of team members with diverse skillsets, while providing functional & technical guidance and SME support Ability to manage projects from end-to-end, from requirements gathering through implementation, hypercare, and development of support processes to ensure longevity of solutions Demonstrated experience interfacing with internal and external teams to develop innovative data science solutions Strong understanding of data science development lifecycle (CRISP) Deep experience with CI/CD integration (e.g. GitHub, GitHub Actions or Jenkins) Deep understanding of MLOps principles and tech stack (e.g. MLFlow) Experience working in a cloud based analytics ecosystem (AWS, Snowflake, etc) Highly self-motivated to deliver both independently and with strong team collaboration Ability to creatively take on new challenges and work outside comfort zone Strong English communication skills (written & verbal) Preferred Qualifications Advanced degree in Data Science, Computer Engineering, Computer Science, Information Systems or related discipline Experience in solution architecture & design Experience in software/product engineering Strong hands-on skills for data and machine learning pipeline orchestration via Dataiku (DSS 10+) platform Hands on experience working in Agile teams, processes, and practices Pharma & Life Science commercial functional knowledge Pharma & Life Science commercial data literacy Experience with Dataiku Data Science Studio Ability to work non-traditional work hours interacting with global teams spanning across the different regions (eg: North America, Europe, Asia) Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Information & Business Tech

Do you want to make an impact on patient health around the world? Do you thrive in a fast-paced environment that brings together scientific, clinical, and commercial domains through engineering, data science, and analytics? Then join Pfizer Digital’s Artificial Intelligence, Data, and Advanced Analytics organization (AIDA) where you can leverage cutting-edge technology to inform critical business decisions and improve customer experiences for our patients and physicians. Our collection of engineering, data science, and analytics professionals are at the forefront of Pfizer’s transformation into a digitally driven organization that leverages data science and advanced analytics to change patients’ lives. The Data Science Industrialization team within Data Science Solutions and Initiatives leads the scaling of data and insights capabilities - critical drivers and enablers of Pfizer’s digital transformation. As the AI and Data Science Production Deployment Lead, you will be a leader within the Data Science Industrialization team charged with driving the deployment of AI use cases and reusable components into full production. You will lead a global team and partner with cross-functional business stakeholders and Digital leaders to catalyze identification, design, iterative development, and continuous improvements of deployment processes to support production data science workflows and AI applications. Your team will define and implement standard processes for quality assurance, testing, data ops, model ops, and dev ops while also providing SDLC, support, platform engineering, and cloud engineering guidance as needed. In addition, you will be responsible for providing critical input into the AI ecosystem and platform strategy to promote self-service, drive productization and collaboration, and foster innovation. Your team will be accountable to key Pfizer business functions (including Pfizer Biopharma, R&D, PGS, Oncology, and Enabling Functions) for production deployments of data science workflows and AI solutions that support major business objectives across all of Pfizer’s core business units. Role Responsibilities Lead deployment of production AI solutions and reusable software components with automated self-monitoring QA/QC processes Implement QA and testing, data ops, model ops, and DevOps for data science workflow products, industrialized workflow accelerators, and best practices in the production deployment of scalable AI/ML analytic insights products Enforce best practices for QA and testing and SDLC production support to ensure reliability and availability of deployed software Act as a subject matter expert for production deployment processes of data science workflows, AI solutions, and reusable software components on cross functional teams in bespoke organizational initiatives by providing thought leadership and execution support Direct QA and testing, data ops and model ops, DevOps, platform and cloud engineering research, advance data science workflow CI/CD orchestration capabilities, drive improvements in automation and self-service production deployment processes, implement best practices, and contribute to the broader talent building framework by facilitating related trainings Set a vision, prioritize workstreams, and provide day-to-day leadership, supervision, and mentorship for a global team with technical & functional expertise that includes QA and testing, DevOps, data science, and operations Coach direct reports to adopt best practices, improve technical skills, develop an innovative mindset, and achieve professional growth through technical and organizational thought leadership Communicate value delivered through reusable AI components to end user functions (e.g., Chief Marketing Office, Biopharma Commercial and Medical Affairs) and evangelize innovative ideas of reusable & scalable development approaches/frameworks/methodologies to enable new ways of developing and deploying AI solutions Partner with other leaders within the Data Science Industrialization team to define team roadmap and drive impact by providing strategic and technical input including platform evolution, vendor scan, and new capability development Partner with AI use case development teams to ensure successful integration of reusable components into production AI solutions Partner with AIDA Platforms team on end to end capability integration between enterprise platforms and internally developed reusable component accelerators (API registry, ML library / workflow management, enterprise connectors) Partner with AIDA Platforms team to define best practices for production deployment of reusable components to identify and mitigate potential risks related to component performance, security, responsible AI, and resource utilization Basic Qualifications Bachelor’s degree in AI, data science, or engineering related area (Computer Engineering, Computer Science, Information Systems, Engineering or a related discipline) 10+ years of work experience in data science, or engineering, or operations for a diverse range of projects 2-3 years of hands-on experience leading data science or AI/ML deployment and operations teams Track record of managing stakeholder groups and effecting change Recognized by peers as an expert in production deployment and AI/ML ops with deep expertise in CI/CD and DevOps for monitoring and orchestration of data science workflows, and hands-on development Understands how to synthesize facts and information from varied data sources, both new and pre-existing, into clear insights and perspectives that can be understood by business stakeholders Clearly articulates expectations, capabilities, and action plans; actively listens with others’ frame of reference in mind; appropriately shares information with team; favorably influences people without direct authority Clearly articulates scope and deliverables of projects; breaks complex initiatives into detailed component parts and sequences actions appropriately; develops action plans and monitors progress independently; designs success criteria and uses them to track outcomes; engages with stakeholders throughout to ensure buy-in Manages projects with and through others; shares responsibility and credit; develops self and others through teamwork; comfortable providing guidance and sharing expertise with others to help them develop their skills and perform at their best; helps others take appropriate risks; communicates frequently with team members earning respect and trust of the team Experience in translating business priorities and vision into product/platform thinking, set clear directives to a group of team members with diverse skillsets, while providing functional & technical guidance and SME support Ability to manage projects from end-to-end, from requirements gathering through implementation, hypercare, and development of support processes to ensure longevity of solutions Demonstrated experience interfacing with internal and external teams to develop innovative data science solutions Strong understanding of data science development lifecycle (CRISP) Deep experience with CI/CD integration (e.g. GitHub, GitHub Actions or Jenkins) Deep understanding of MLOps principles and tech stack (e.g. MLFlow) Experience working in a cloud based analytics ecosystem (AWS, Snowflake, etc) Highly self-motivated to deliver both independently and with strong team collaboration Ability to creatively take on new challenges and work outside comfort zone Strong English communication skills (written & verbal) Preferred Qualifications Advanced degree in Data Science, Computer Engineering, Computer Science, Information Systems or related discipline Experience in solution architecture & design Experience in software/product engineering Strong hands-on skills for data and machine learning pipeline orchestration via Dataiku (DSS 10+) platform Hands on experience working in Agile teams, processes, and practices Pharma & Life Science commercial functional knowledge Pharma & Life Science commercial data literacy Experience with Dataiku Data Science Studio Ability to work non-traditional work hours interacting with global teams spanning across the different regions (eg: North America, Europe, Asia) Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. 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Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Scientific Director, Clinical Pharmacology Scientific Director, Clinical Pharmacology position in Quantitative Pharmacology within the broader Clinical Measurement Sciences organization is a strategic, scientific, and cross-functional role, leading the Clinical Pharmacology (CP) Expert Team, responsible for developing and executing clinical pharmacology and Model Informed Drug Development (MIDD) strategies from the early to late-stage clinical development. This role represents the CP Expert Team to the global cross functional drug discovery and development project teams, in close collaboration with colleagues in Biostatistics, Data Sciences, Clinical Biomarkers and Diagnostics, Research, Clinical Development and other colleagues within the R&D organization. The CP Expert Team Lead provides strong leadership for integrating individual functional contributions, developing clinical pharmacology strategy in alignment with the overall clinical development plan, and executing the program strategy/plan. The scope includes programs from exploratory development (ED) through life cycle management, encompassing large and small molecule therapeutics/drug candidates across different therapeutic areas. KEY ACCOUNTABILITIES Ensures that CP strategy is developed, aligned (with cross-functional development plans), endorsed and executed to support the indication, patient population, and phase of development while taking into account the competitive landscape Represent clinical pharmacology and promote MIDD with internal and external stakeholders Provides in-depth CP, PK and PK/PD advice and expertise and lead clinical pharmacology expert team and deliver on Dose and posology decisions, from FIH starting dose through submission and beyond Fit-for-purpose CP package including dose, dose regimen, and adjustment for specific conditions and specific populations, exposure-QTc assessment and immunogenicity assessment in collaboration with other function lines at appropriate stages of development Develop and execute MIDD strategies/plans in collaboration with pharmacometrics and other functions PK/PD data analysis, interpretation, and presentation Related sections of major clinical and regulatory documents (e.g. clinical protocols, IBs, CTDs, INDs, NDAs, IMPDs, briefing books) Contribute to due diligence projects, if needed EDUCATION/LANGUAGES 7+ years (Bio)pharmaceutical industry and/or postdoctoral experiences with clinical drug development experience Doctorate degree (PhD, PharmD or MD) relevant in the related disciplines of clinical pharmacology, pharmaceutics, pharmacometrics, statistics, engineering or mathematics Fluency in English PROFESSIONAL SKILLS & EXPERIENCE Strong understanding of clinical drug development strategies, and quality related requirements in drug development in GXP-related areas. Deep knowledge in CP, i.e., PK, ADME, posology, quantitative translational sciences, etc. Excellent knowledge of regulatory requirements and submission across the main regions Good understanding about translational sciences such as quantitative pharmacology, safety and biomarkers. Clear evidence of ability to adapt to changing business needs by prioritizing multiple tasks. General knowledge of oncology, immuno-oncology, and/or immunology, and more in depth understanding of biology and pharmacology is a plus. Hands on modeling expertise is a plus. Strong interpersonal skills and proactivity to cultivate a network of productive relationships in an international matrix environment. Demonstrated ability for productive collaboration in a multi-discipline team, using effective communication and taking personal accountability for timely delivery of results. Strong presentation, communication, and organization skills. Ability to communicate technical results to stakeholders. have a broad scientific understanding across the translational sciences and drug development along with excellent team-building skills and strong collaborative & strategic capabilities. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Job Summary : Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we’re looking for experienced professionals to join us as we prepare to launch of our newest office in Hyderabad, India . This is more than just a job. It’s an opportunity to be part of something from the very beginning. You’ll play a direct role in shaping the culture, building the team, and influencing how we grow in India. From day one, your work will make a meaningful impact across global projects. Why Join Medpace in Hyderabad? Be a Founding Member : Help establish and lead operations at our newest location. Immediate Impact : Your experience will directly influence Medpace’s growth in the region. Career Growth : As the office grows, so will the leadership and advancement opportunities. Global Reach : Work on cutting-edge clinical trials with international teams and top-tier sponsors. Strong Culture : Join a company known for its stability and commitment to professional development. Support & Infrastructure : While the Hyderabad office is new, you’ll be backed by the global resources and processes of a well-established CRO. If you’re looking for a new challenge, and want to be part of building something meaningful while advancing your career with a company that’s investing in your region — we’d love to hear from you. Help shape the future of Medpace in Hyderabad. Apply today. Responsibilities : Collect, analyze and document user requirements; Design, modify, develop and support software applications; Participate in software validation process through development, review, and/or execution of test plan/cases/scripts; Create software applications by following software development life-cycle, which includes requirements gathering, design, development, testing, release, and maintenance; Communicate with team members regarding projects, development, tools, and procedures; Utilize skills in development areas including object oriented programming (C#), databases (SQL) web applications (ASP.NET); and Potential opportunities to lead software development projects. Qualifications : Bachelor's Degree in Computer Science; Familiarity of technologies such as C#, Angular, Webservices, Git, relational databases; Experience in Entity Framework, Azure DevOps is advantageous; Understanding of software development life cycle (SDLC) and software release management; Prior experience modernizing systems to a cloud-based platform (Azure) is a plus; Excellent analytical, written and oral communication skills in English; and Prior experience developing mobile application (iOS/Android) is a plus. Medpace Overview : Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Key Accounts Manager -Oncology-( Calicut ) Domnic Lewis has been mandated to hire for Key Accounts Manager -Oncology-( Calicut ) Role Overview A high-performing sales professional with demonstrated impact beyond their immediate geography. This individual serves as a mentor to peers, consistently introduces best practices, and drives strong performance across the region. Key Responsibilities Complete all mandatory training programs and product certifications successfully. Engage with oncology healthcare professionals to provide scientific information on approved indications, efficacy, and safety to support appropriate on-label use. Collaborate with the Sales Manager to design and execute territory-specific strategies and business plans to exceed sales targets and call execution goals. Deliver strong sales performance and ensure sales forecasts and budgets are consistently met or surpassed. Maintain a comprehensive understanding of the territory//'s market landscape, customer demographics, and managed care environment. Uphold full compliance with company policies and regulatory requirements, particularly in healthcare professional interactions and sample distribution. Qualifications Essential: Bachelor//'s degree (Science/Pharmacy preferred) Minimum 3 years of experience in Oncology sales Desirable: Experience with a multinational pharmaceutical Oncology company (MNC) Currently managing or experienced in the Oncology portfolio

Paediatric Oncology Nutritionist Cuddles Foundation brings holistic nutritional counselling to children fighting cancer across India. As a Cuddles Nutritionist, you’ll get a chance to improve treatment outcomes of children in government and charity cancer hospitals alongside award-winning oncologists and clinicians. So, being organised, flexible, and prioritising your time will be vital. Responsibilities: → You’ll manage out-patients and in-patients in the Paediatric Oncology and Hematology departments. → You’ll assess the child’s health needs and diet, complying with the guidelines outlined in our training manual. This includes anthropometric examinations, such as measuring height, weight, BMI and assessing the child’s nutritional status and deficiencies. → You’ll develop diet plans for every child, involving the child and the family, based on a careful analysis of their medical condition and required growth and development. → You’ll maintain detailed records of your counsel for mapping success, monitoring and evaluation, and publishing case studies. → You’ll conduct weekly group counselling sessions, and parent support meets to help caregivers cope with treatment conditions and inspire good food habits to prevent or manage infections. → You’ll distribute aid initiated by Cuddles at the hospital, including monthly ration, eggs, bananas, dry fruits, milk, etc. → You’ll participate in meetings and training programs conducted by the organisation and be open to learning, assignments and evaluations. → You’ll keep up with the latest nutritional science research. → As a representative of Cuddles at the hospital, you will collaborate with the doctors and nurses while reporting to your team lead regularly. → You’ll ensure patient satisfaction, quality care, regulatory compliance, and efficient use of resources. Must-Haves: → A Master’s or Diploma in Clinical Nutrition and Dietetics. → At least a 6-month internship at a multispecialty hospital and 1.5 years work experience. → Fluency in the Hindi & English language. → Excellent verbal and written communication skills, with exceptional attention to detail. → Willing to commit to at least 18 months of work. → Proficient with Microsoft Excel. → Ability to work in a team and have a strong work ethic. Skills: You’re a great listener A large part of your work as a paediatric nutritionist will depend on what children tell you or don’t tell you. You have to be empathetic to what they and their parents are going through. You are an influencer and a champion for good nutrition at all times. You are a champ at influencing people. People come to you for advice. You will inspire parents, children, and even doctors to follow good nutrition practices in your day-to-day work. You believe food heals. You have a knack for dealing with kids. You are patient and compassionate. You can tell a good story and inspire children to eat right. You don’t talk down to them. You are their advocate and friend. Data doesn’t scare you. You will have to keep a keen eye on nutritional data, malnourishment status, calorie counts and deficiencies of your patients. You have a knack for technology. We love tech when it makes your life easy. We solve the malnutrition problem in critical illnesses through our FoodHeals App. You will be using this in your day-to-day work. You’re a stickler for organising things. You have remarkable attention to the slightest detail and meticulous organisational skills. Your closet and drawers are a testament to this skill: when something doesn’t have a place, you make one for it and teach others to keep it that way. You can manage schedules, prioritise your work and follow it with minimum supervision. Job Types: Full-time, Permanent Pay: ₹28,000.00 - ₹30,000.00 per month Benefits: Health insurance Schedule: Day shift Ability to commute/relocate: Ansari Nagar, Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required) Education: Master's (Required) Experience: total work: 2 years (Required) Work Location: In person

Opportunity with an Esteemed Client Company of Sanskruti Solutions (Diagnostic Setup): Job Position: Genomic Application Specialist (Field Job) Work Location: Delhi - NCR HQ / Hyderabad HQ but travelling is required across various cities within India to communicate with Oncologists Doctors. Brief Role Description: As a Genomic Application Specialist, you will play a pivotal role in bridging the gap between complex genomics and the medical field. Your primary focus will involve facilitating Oncologists, Patients, Genetic Counsellors', Sales Team in comprehending genomic reports and leveraging this knowledge for informed decision-making in cancer treatments. Key Responsibilities: Scientific Communication: Engage with treating Oncologists explaining the details of genomics reports and molecular interpretations in an understandable manner. Oncologist Collaboration: Work closely with Oncologists to ensure a thorough understanding of our products, their scientific foundations and the distinctions of report interpretation. Travel Commitment: Be prepared to travel across different cities within India with a sales team to facilitate seamless communication and collaboration with Oncologists. Must to have Qualifications / Experience Criterias': PhD. in Genetics / Cellular Biology / Genomics / Bioinformatics / Computational Biology is a must. Preferred 0 to 3 years of experience in Cancer Genomics, Oncology field after PhD. Experience in Genomics, Cancer Genomics is a must. Fluent communication in English is a must and understanding of regional languages will be positive. Willingness to travel around different cities for communicating with Oncology Doctors. Job Types: Full-time, Permanent Pay: ₹750,000.00 - ₹1,200,000.00 per year Benefits: Commuter assistance Health insurance Provident Fund Schedule: Day shift Fixed shift Application Question(s): Have you read the job description for this post? Where are you currently based in India and you have applied for which job location? If not based in Delhi - NCR / Hyderabad then are you comfortable with relocation to Delhi - NCR / Hyderabad and managing your self-accommodation arrangements from the offered CTC? Are you a PhD Holder? Do you have 0 to 3 years of experience in Cancer Genomics, Oncology after PhD? How many years of experience do you have in the Cancer Genomics field? This job requires extensive traveling in the assigned business territories within HQ City as well as in different parts of India for meeting Oncologist Doctors for doing scientific communications with them, are you comfortable with this? Are you available with an immediate joining? Please provide the following details viz. Reason for job change now, Current CTC, Expected CTC, Notice Period for joining: Do you have any other job offers in hand now? If yes, then provide its details without revealing the company name and update us why you are not accepting that job offer? Which Languages do you speak now? Give your self-rating out of 10 for each language being spoken by you? Why do you think this opportunity is the right opportunity for you and if considered positively for this role and if selected, do you think you can associate from long term perspective as we don't want someone coming with short term duration: Work Location: In person

Key Accounts Manager -Oncology - Jaipur Domnic Lewis has been mandated to hire for Key Accounts Manager -Oncology - Jaipur Role Overview A high-performing sales professional with demonstrated impact beyond their immediate geography. This individual serves as a mentor to peers, consistently introduces best practices, and drives strong performance across the region. Key Responsibilities Complete all mandatory training programs and product certifications successfully. Engage with oncology healthcare professionals to provide scientific information on approved indications, efficacy, and safety to support appropriate on-label use. Collaborate with the Sales Manager to design and execute territory-specific strategies and business plans to exceed sales targets and call execution goals. Deliver strong sales performance and ensure sales forecasts and budgets are consistently met or surpassed. Maintain a comprehensive understanding of the territory//'s market landscape, customer demographics, and managed care environment. Uphold full compliance with company policies and regulatory requirements, particularly in healthcare professional interactions and sample distribution. Qualifications Essential: Bachelor//'s degree (Science/Pharmacy preferred) Minimum 3 years of experience in Oncology sales Desirable: Experience with a multinational pharmaceutical company (MNC) Currently managing or experienced in the GUGYN (Gynecologic & Urologic Oncology) portfolio