3564 Oncology Jobs - Page 46

Company Description Sahyadri Hospitals currently operates 11 hospitals with over 1,200 beds, serving more than 2,500 clinicians and 3,000 support staff. The network has touched 5 million lives and excels in areas like Neurosciences, Haematology, Oncology, Cardiology, Orthopaedics, General Surgery, and more. The Sahyadri Hospital Network includes facilities in Deccan Gymkhana, Hadapsar, Nagar Road, Bibwewadi, Kothrud, Nashik, Ahilya Nagar, Karad, Kasba Peth, and Hadapsar Annexe. Role Description This is a full-time, on-site role based in Pune for a Scrub Nurse. The Scrub Nurse will be responsible for assisting during surgeries, maintaining sterile environments, preparing operating rooms, handing instruments to surgeons, and ensuring patient care before, during, and after procedures. Qualifications Nursing and Medicine skills Experience in Orthopedic Surgery and general Surgery Proficiency in Operating Room procedures Excellent communication and interpersonal skills Ability to work well in a high-pressure environment Registered Nurse (RN) license required Bachelor's degree in Nursing or a related field is preferred Previous experience as a Scrub Nurse is a plus

Roles and Responsibilities Provide high-quality patient care as a senior resident in onco surgery department. Assist consultants during surgeries, procedures, and rounds. Participate in multidisciplinary team meetings to discuss patient cases and treatment plans. Develop clinical skills by observing and assisting experienced surgeons during complex operations. Maintain accurate records of patient data, test results, and treatment outcomes.

Job Title: Global Lead Buyer Events & Medical Communication Location: Hyderabad Sanofi is an innovative global healthcare company headquartered in Paris, France with one purpose: Chase the miracles of science to improve people’s lives. We are dedicated to making a positive impact on the lives of the patients and families we serve, and we accomplish our goals through world-class research and with the compassion and commitment of our employees. The company is focused on accelerating development to deliver breakthrough medicines and vaccines to patients, delivering excellence though Diversity. Sanofi operates in 90 countries with 91 000 employees worldwide, working in 59 manufacturing and 20 Research & Development (R&D) sites. In 2022 business net income was €10.3 Billion, delivered by 4 Global Business Units: Specialty care, Consumer Healthcare, Vaccines & General Medicines. Sanofi covers major therapeutic areas, including immunology, cardiovascular, diabetes, oncology, rare diseases, etc. Within Sanofi, the Procurement function is a powerhouse maximizing savings to fund the company’s future growth. The Chief Procurement Officer is reporting to the Chief Financial Officer, member of the sanofi executive committee. The Procurement organization is divided into five Domains (Manufacturing & Supply, Marketing & Sales, Professional Services, Scientific & Medical and Digital) leveraging Global Procurement Operations and the Procurement Center of Excellence & Transformation. The yearly spend coverage is around 15B€ with a special focus on Procurement excellence, Supplier Diversity and Sustainability. Closely collaborating with Finance, Business Operations and Business Units, Procurement is instrumental in achieving cost efficiency and savings. Procurement plays a critical role in optimizing Business Operational Impact with a focus on driving simplification, efficiency, and productivity. It forges strategic partnerships with suppliers, prioritizing innovation and data driven solutions. About the job The Global Lead Buyer Events & Medical Communication is responsible for developing Global category strategies. He/She guarantees that best market value is captured and incorporate in Sanofi with clarity on execution excellence and alignment with his Global or key Local Stakeholders across GBUs, GTMC and SBO. This role is global with frequent coordination of actions at local level to ensure adaptation and executability of the Global strategies. This includes activities such as, but not limited to, partnering with the internal stakeholders (Global and cross-categories procurement, business, Finance), assist with building project scopes based on business needs in compliance with Global procurement strategy and preferred supplier, conduct Global Request for Proposal (RFP), negotiate contracts, rate cards / discount schedules, ensure building a strong savings pipeline including rigor on tracking, reporting and validation by Finance, manage overall relationships with key suppliers (performance evaluations, QBRs, action plans, SRM programs) The Events and Medical Communications Agencies category includes all spend natures related to internal and external events, Booths, publications, Scientific Engagement, Medical Communications services, targeted communications, production & adaptation. Main focus of this role will be to: Support Events & Medical Communication services transformations by delivering best in class sourcing strategy(ies)Business partnering with the Sanofi Business Operations Hub leaders, Global meeting & Events, and Key GBUs/R&D stakeholders. Support Events optimization drivers execution in International Regions and key markets as needed. ABOUT YOU Operations Management : Supports others Global Lead Buyer or the Regional Category Manager of the category to ensure strategy's execution. Lead Market analysis and capture market value. Delivers savings pipeline in line with targets. Leads RFIs/RFPs and contract negotiations for his/her category. Leads local transformational projects according to Category Management with ability to connect any markets to global needs. Reports on status, savings, performance, and risks on the sourcing activities he/she is in charge of including regular touchpoints with Finance business partners. Undertakes benchmarking against other industries and best practices. Run SRM program with suppliers of his/her scope. Support pre/post-audit management, Crisis management. Maintains comprehensive understanding of Procurement Policies/Processes related to Risk/CSR/Compliance and ensures that these are adhered to by relevant team members. Identifies non-compliant processes and defines appropriate corrective measures Stakeholder Management: Develops strong partnerships with his/her key internal customers, including senior management and foster two-way supportive relationships with them. Presents Procurement strategies to key internal customers for review and input. Identify cross-GBU synergies even in absence of cross-GBU stakeholders Experience: 5+ years’ experience in Procurement or related field (including agency-side experience). Knowledge of Pharma Industry Soft Skills/ Technical skills: The position requires sourcing professional skills with a strong ability to develop relationships within and across the different lines of business and throughout the Procurement organization, including transversal / project management skills as well as management skills in a multi-cultural environment. Knowledge of best-in-class Procurement techniques and processes. Experience with Procurement Systems (eg SAP, Coupa). Consistency of focus upon delivery of outcomes and results. Demonstrated analytical skills and ability to utilize tools/systems accordingly. Ability to work independently on multiple concurrent priorities/projects Defines and balances strategic priorities against immediate operational challenges. Able to quickly assimilate new information/skills. Readily adapts to new environment, processes, ways of working, etc. Willingness and ability to challenge the status quo. Creativity in imagining new processes, innovative ideas, and solutions. Possesses strong competency in partnering with various stakeholders to deliver successful outcomes Encourages collaboration within team and across other functions/groups. Strong planning, problem-solving and responsive decision-making skills. Strong communication, presentation, change management and negotiation skills. Role model in compliance and ethics. Actively seeks feedback to identify opportunities for improvement. Resilience and aptitude to navigate in a complex organization Education : Minimum Bachelor’s degree from accredited University (master's degree is preferred) Languages: Fluent in English is a must. Pursue Progress . Discover Extraordinary . 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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue Progress. And let’s 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, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Job title: Expert Quality Services (Product Complaints) Location: Hyderabad About the job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people in over 100 countries at Sanofi are dedicated to making a difference on patients’ daily life, wherever they live and enabling them to enjoy a healthier life. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting Global M&S teams in partnership with Business and Digital, and drive priority and transformative initiatives across M&S. The team members of Global M&S Services Hubs will act as partners in carrying out tasks and fulfilling responsibilities to support identified and established global quality processes from the hubs. Main responsibilities: Handle Product Technical Complaints and Field Alerts for medical devices, pharmaceutical products, biologics, and combination products, ensuring compliance with regulatory standards. Manage the entire process of handling Product Technical Complaints and Field Alerts from receipt to closure, ensuring compliance with internal procedures and regulatory requirements. Collaborate with internal and external manufacturing sites, Customer Service, Medical Information, Pharmacovigilance, Sales Associates, Regulatory, Commercial Operations, Legal, and Risk Management departments. Evaluate complaints for severity and risk, ensuring timely review and processing. Prioritize and enter complaints into the global database, monitoring complaint activity for assigned manufacturing sites. Produce monthly reports for manufacturing sites on complaint activity and support during audits and regulatory inspections. Participate in ad-hoc teams for product-specific complaint issues and provide feedback on complaint investigations. Focus on operational tasks within the compliant handling process. Identify and implement continuous improvement opportunities. Provide regulatory interpretation and guidance to internal teams. Manage and oversee the training within the department. Perform quality checks on PQC activities, prepare reports, and maintain inspection readiness. About you: Experience: 6 – 10 years of related experience in the pharmaceutical industry. Knowledge of cGMP’s, Code of Federal Regulations in drugs and biologics, and complaint database software and reporting tools. Should be knowledgeable in Quality functions of pharmaceutical industry. Experience of working on manufacturing sites is an added advantage. Proficient in problem-solving, attention to detail, and good organizational skills. Work in a team-oriented, flexible, and proactive manner. Analytical skills and ability to multitask in a stressful environment. Education: Bachelor’s or Masters in Life Sciences/Healthcare, Business Administration, Engineering or Information Technology. Languages: Verbal and written fluency in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks’ gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas.

Job Title: Specialized Support Lead Job Location: Hyderabad About the job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. Ready to push the limits of what’s possible? Join Sanofi in one of our corporate functions and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world. As Specialized Support Lead within our People Tech Solutions Team. We are looking for an experienced Specialized Support Lead to oversee and manage Level 2 technical support operations but also workday mass load, etc. This role ensures timely resolution of complex issues, collaborates with cross-functional teams, and drives service excellence. The ideal candidate has strong troubleshooting skills, leadership experience, and a commitment to improving support processes. Main responsibilities: Incident Management & Troubleshooting : Handle escalated technical issues that require in-depth analysis and resolution. Work closely with L1 support teams to ensure seamless issue escalation and resolution. Investigate recurring problems and implement permanent solutions. Team Leadership & Mentoring: Lead and mentor the support team to enhance their technical expertise. Conduct training sessions to improve troubleshooting skills and knowledge sharing. Ensure adherence to SLAs (Service Level Agreements) and performance metrics. Collaboration & Stakeholder Engagement: Coordinate with development, infrastructure, and business teams for complex issue resolution. Provide technical guidance to L1 teams and ensure smooth handover to L3 when necessary. Communicate issue updates and resolutions to stakeholders clearly and effectively. Process Improvement & Automation: Identify areas for process improvement in support workflows. Recommend and implement automation tools to enhance efficiency. Maintain documentation of known issues, solutions, and best practices. Monitoring & Reporting: Track and analyze incident trends to prevent future occurrences. Generate reports on support team performance and key operational metrics. Ensure compliance with ITIL best practices and company policies. About you Bachelor's degree in computer science , Information Technology , or a related field. 5+ years of experience in IT support, service desk, or technical troubleshooting , with at least 2 years in a leadership role. Strong expertise in Workday, Learning and other HRS connected global tools such as work human, skyhive etc. Experience with ITSM tools (e.g., ServiceNow, Jira, Remedy) and ticketing systems. Knowledge of ITIL framework and best practices for IT service management. Excellent problem-solving, analytical, and communication skills. Ability to work in a fast-paced environment and manage multiple priorities effectively. Why choose us? Join our innovative team where collaboration is at the heart of everything we do. You'll work closely with talented professionals, tackling complex issues and finding creative solutions together. Our supportive environment ensures that your ideas are heard and valued, fostering a culture of teamwork and mutual respect. We prioritize continuous learning and growth, offering opportunities for professional development and career advancement. Our comprehensive benefits package, including health insurance, retirement plans, and flexible work arrangements, supports your well-being both at work and at home. Be part of a team that values excellence, innovation, and collaboration. Together, we'll achieve great things and make a real impact.

Conducts an individualized patient assessment, prioritizing the data collection based on the patient’s immediate condition or needs within the time frame specified by policies, procedures or protocols Develops care plan for all patient assigned, post assessment and does re-assessment. To prepare and administer (orally, subcutaneously, through an IV) and record prescribed medications. To report adverse reactions to medications or treatments in accordance with the policy regarding the administration of medications. To record patients’ medical information and vital signs appropriately. To assess the patients’ ability to do routine daily tasks. To assist patients with basic needs such as dressing, eating, and bathing, and to encourage patients to do things for themselves to retain feelings of independence and self-esteem. To take care of patients with surgical wounds and different drain To recognize and manage end of life care patient including : cardiovascular, respiratory, gastrointestinal, urinary, haematology, muscular-skeletal, endocrine, neurological, psychiatric/psycho-social, sensory and pain problems. To assist patients in bathing, grooming. Guide PCA to help patients mobilize to and from the toilet, to change patient’s diaper if bed-bound. To take extreme care to maintain a patient’s dignity and privacy at all times. To prepare equipment and aid physician during examination and treatment of patient. To meet patients nutritional needs (RT feeding, PEG feeding, NJ feeding To involve, educate, and when appropriate, supervises family/significant others in implementing best practices for older adults. Initiates emergency measures according to adult resuscitation protocols To promote the desirability of quality end-of-life care for older adults. To record all care information concisely, accurately and completely, in a timely manner, in the appropriate formats. To practice at a high level of accountability in collaboration with oncologists to provide a continuum of patient care from prevention, early detection, diagnosis, treatment, follow-up, palliation, bereavement and survivor-ship of cancer patients. To possess a sound knowledge base of chemotherapy: protocols, regimens, action & side effects, administration, precautions to be taken, spill management etc. To be skilful in the solubilization and administration of chemotherapeutic drugs. BMT To provide comprehensive orientation, education and counselling to transplant patients and family prior to transplant. To possess the knowledge and skill of caring for patients receiving Bone Marrow Transplantation: peripheral blood stem cells, autologous and allogenic transplants. To have in-depth knowledge on the various complications and the management of the same post BMT: graft rejection, infection, pneumonitis, nonocclusive diseases, GVHD, etc. To provide care for patients with alteration in protective mechanisms: neutropenia, thrombocytopenia, altered skin integrity, neuropathy etc. To be responsible in collaboration with the transplant consultant for the efficient organisation and coordination of pre transplant investigations for transplant patients. To liaise with Cannulation & Apheresis Treatment Team, Day Oncology and inpatient ward areas to facilitate the collection of autologous cells and the admission of transplant patients. To facilitate the referral of patients for consideration of allogeneic BMT and coordinate the transfer of their care. To accept referrals from medical staff on potential bone marrow transplant recipients and co-ordinate the presentation of these patients at unit review meetings. To Coordinate and, together with medical and other staff, provide a comprehensive program of care for transplant recipients including vaccinations, long-term effects etc. To provide patient and family education and counselling upon discharge and follow up as necessary To facilitate holistic care and integrated service provision to patients undergoing a BMT. To participate in and promote family meetings with the multi-disciplinary team. To ensure patient care standards meet professional, organizational, legal and ethical requirements. To ensure confidentiality of client information. •To assist in the on-going review of nursing and medical leukemia and BMT policies and procedures. •To maintain on-going personal and professional development by undertaking further education as required, attending lectures and meetings. To provide on-going information to patients and carers to assist them in understanding their disease process and subsequent plan of care. Job Type: Full-time Pay: ₹25,000.00 - ₹32,000.00 per month Benefits: Food provided Provident Fund Schedule: Rotational shift Experience: Registered Nurse: 1 year (Required) License/Certification: Karnataka Nursing Council Registration (Required) Work Location: In person

Job Summary: We are seeking a detail-oriented and enthusiastic Dietitian to assess, plan, implement, and monitor individualized nutrition care plans for patients, with a focus on oncology and specialty care, ensuring optimal nutritional support to enhance recovery and improve quality of life. Key Responsibilities: Conduct nutritional assessments for inpatients and outpatients, especially cancer and specialty care patients. Develop and implement individualized diet plans based on patients’ medical condition, treatment plan, and preferences. Collaborate with physicians, nurses, and other healthcare professionals to integrate nutrition into comprehensive patient care. Monitor patient progress and modify diet plans as needed. Provide nutrition counseling and education to patients and their families. Ensure that therapeutic diets are accurately prepared and served. Assist in menu planning, recipe standardization, and quality assurance related to hospital meals. Maintain accurate patient records and documentation. Participate in multidisciplinary case discussions and clinical audits. Support hospital programs related to patient wellness, preventive care, and nutrition awareness. Qualifications: Education: B.Sc./M.Sc. in Nutrition & Dietetics or Clinical Nutrition from a recognized university. Certification: Registered Dietitian (preferred) or certified by a recognized Dietetics council / association. Experience: Minimum 1–3 years in a clinical/hospital setting. Experience in oncology nutrition is an advantage. Candidates preferably from Dharmapuri location, Tamilnadu. Candidates must fluent in Tamil Language No of Requirement: 1 Number Salary: ₹10,000 - ₹15,000 a month (Negotiable based on the experience & Skill metrics) Note: Please forwarded your updated resume to hr@vijaysuperspecialityhospital.in and feel free to reach to (+91 91507 51668) us for further information. Job Types: Full-time, Permanent Pay: ₹10,000.00 - ₹15,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person

Consultant 2=5 Yrs 1 Palanpur, 385001 Job Description Key Responsibilities Evaluate patient medical histories and diagnostic imaging to determine treatment suitability Design personalized radiation treatment plans using advanced planning software Collaborate with medical physicists, dosimetrists, and radiation therapists to ensure precise delivery Monitor patient progress and adjust treatment protocols as needed Educate patients and families about treatment options, risks, and side effects Participate in tumor boards and multidisciplinary case discussions Maintain detailed records and ensure compliance with safety standards Engage in clinical research and stay updated on emerging therapies Required Skills & Competencies Deep understanding of radiation physics, oncology, and radiobiology Proficiency in using linear accelerators and treatment planning systems Strong communication and empathy for patient-centered care Analytical thinking for complex treatment decisions Team collaboration across oncology disciplines Commitment to continuous learning and innovation Qualifications Requirement Details Education MBBS + MD/DNB in Radiation Oncology Certification Board certification (e.g., MCI, NMC) Experience Residency + 1–2 years clinical experience Work Environment Hospitals, cancer centers. Often part of a comprehensive cancer care team Full Time 2000k Year Radiation Oncology Contact us For more information, contact us on admin@vitalityhealthcare.in

Radiopharmaceutical Handling: Prepare and administer radioactive drugs to patients in accordance with safety protocols. Ensure proper dosage, timing, and documentation of radiopharmaceuticals. Imaging Procedures: Conduct nuclear imaging procedures including PET, SPECT, and planar imaging. Assist in hybrid imaging techniques (e.g., PET/CT, SPECT/CT) used for tumor localization and therapy planning. Position patients and operate imaging equipment to obtain high-quality diagnostic images. Oncology-Specific Applications: Perform functional imaging to detect primary and metastatic cancer. Assist in dosimetry calculations and monitoring during radionuclide therapy (e.g., I-131, Lu-177, Y-90 treatments). Collaborate with oncologists and radiologists to support personalized cancer treatment plans. Patient Care and Safety: Educate and prepare patients for nuclear medicine procedures. Monitor patient condition during procedures and respond to any adverse reactions. Practice radiation safety techniques to minimize exposure to patients, staff, and self. Quality Control and Compliance: Calibrate and maintain nuclear medicine equipment. Perform quality assurance checks on imaging systems and radiopharmaceuticals. Comply with hospital policies, radiation safety regulations, and accreditation standards. Record Keeping and Documentation: Maintain accurate patient records, dose logs, and procedure documentation. Ensure timely communication of imaging results to medical staff. Job Types: Full-time, Permanent Pay: ₹60,000.00 - ₹120,000.00 per month Work Location: In person

Job Description Key Account Manager THE OPPORTUNITY Key Account Manager is responsible for Efficiently manage the therapy area by effectively reaching out to customers and increases product awareness, answer queries and introduce new products. Also responsible for Customer Focus and have industry knowledge and schedule and plan the frequency of calls and personally visit the targeted doctors as per agreed coverage list. Based in Mumbai, named one of the Best Companies for Women in India by Avatar, 2019, 2020 and 2021. Join the premier biopharmaceutical company that has been in Asia Pacific for over 60 years. Our Sales team support our customers by providing clinical information about products, educational information, clinical training programs and resources. We support healthcare providers and healthcare systems meet the goals of the patients in their communities. Your role at our organization is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. What You Will Do Key Responsibilities Customer Focus and Coverage Proficient with the therapy and product related features/benefits including scientific information thereto, so as to effectively communicate with the medical doctors and handle product related customer queries. Actively participate in identifying key and potential medical practitioners and specialists in the respective therapeutic segment in the assigned territory, and prioritize for the purpose of systematic customer coverage so as to generate maximum prescription sales for the company’s range of products as per business plan. Schedule and plan the frequency of calls and personally visit the targeted doctors as per agreed coverage list. Call on the Chemists, wholesalers as the case may be to track in-market sales of the products, booking of orders to ensure timely and adequate availability of products to meet market demand. Utilize customer focused selling techniques (CSSP), continually assessing the knowledge of the customer and strategize to maintain high customer confidence and customer knowledge of company products. Maintain current, approved protocol (CSSP) and promotional materials to be included in sales presentation/ detailing. Contact customers on regular basis and deliver informative sales presentations based on customers need. Constantly explore opportunities to develop new business within assigned therapy area. Sales Performance & Results Achieve and exceed the sales targets on a consistent basis through effective implementation of the sales promotion strategies and follow-up initiatives. Specialist in the product knowledge, therapy knowledge and detailing skills so as to enhance productivity levels as expected by the Company. Carry out Product Visibility and such ancillary or incidental activities related to the Products of the Company or Products of any other Company as may be decided from time to time, in accordance with any arrangement or agreement entered into by the Company with such other Company. Explore opportunities to develop new businesses within assigned therapy area. Planning & Sales Performance Management Tactically plans to generate tertiary demand generation Plans and executes field working as per approved tour programmes so as to cover all stakeholders as per decided frequency Takes follow-up initiatives on feedback and customer service requirements. Handles special product campaigns, new product launch campaigns as per Company’s plans. Covers the Nursing homes, clinics and hospitals as per agreed coverage requirements Collects data on annual budget for medicines, mode of purchase, rate contract/tendering etc. as may be required and takes initiatives to tap these business growth avenues. Assists in the collection of receivables, as per company policy. Key Account Management To nurture strategic relationships with top accounts, so a KAM must possess an in-depth knowledge of the company and its customers. KAMs need to have a strategic perspective that goes beyond short-term gains. They must be able to juggle many moving parts and orchestrate deals and long-term plans that align with a mutually beneficial strategy. Communication Meets Actively participate in Cycle meetings, periodic Sales & Marketing meeting and conventions. Conducts group meetings, medical education camps, speaker programmes as may be necessary from time to time for assigned therapy area. Guides and helps other team members within therapy area to design and execute scientific activities as per experience. Coaching and supervision Actively participate in training, orienting and handholding the new comers To be a Mentor to the Trainees, probationers and freshly inducted sales professionals in the assigned therapy area. Expert in the therapy area and constantly providing guidance and coaching to TMs and STMs as per need. To sanction leave of the sales professionals, as per company procedure. Liaising with the Stockists and distributors in connection with customer service requirements. Provides guidance and coaching to TMs as per need. To approve claims upto prescribed limits of authorized stockists, distributors, retailers in respect of breakages, date expiry, spoilage etc after due verification. In case of larger claims, provide accurate and vital inputs to the Management to take appropriate action. Company, Industry & Product Knowledge Demonstrate above average knowledge of all company marketed products, disease, therapy area, competitor products, promotional strategies and objectives. Develops a clear understanding of the Company’s SOPS and protocols pertaining to his area of work. Imbibes the guidelines pertaining to Adverse Event Reporting and takes prompt action in compliance with the requirements. Market Analysis Maintain quality customer list, current profile of assigned key accounts, key influencers & clinical thought leaders. Execute Marketing Strategies in consonance with Marketing guidelines. Collect Market intelligence, conduct market surveys, participate in special projects etc. Actively seek and display knowledge of key customers in territory and therapy area. Building Relations Lead the scientific engagement of key stakeholders within therapy area so as to establish leading corporate image Develop and maintain strong relationships with customers and build up a healthy rapport with them. Work collectively with other team colleagues in arranging speakers, displays, special programs and CMEs to meet the educational needs of customers. Distribution & Resource Allocation Ensure adequate inventory level with trade partner and take prompt actions to prevent date expiry of products. Adherence to Internal tools & Processes/ Administration /Values Ensure timely submission of daily call report, sales documents, feedback reports, expense reports and other administrative duties are completed in an accurate and timely manner. Adhere and demonstrate Leader behaviors. In the discharge of your responsibilities, you will be required to undertake such other jobs as may be assigned to you by the Management from time to time. What You Must Have Degree in Sciences / B Pharm / Equivalent 5 or more year’s relevant experience (Minimum 3 years’ experience in Oncology Sales) Proven experience in articulating data-driven findings to various audience levels and translating these findings into actionable recommendations. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Not Applicable Shift Valid Driving License Hazardous Material(s) Required Skills Account Management, Account Management, Adaptability, Business, Clinical Experience, Coaching, Customer-Focused, Customer Queries, Customer Relationship Management (CRM), Customer Service Management, Demand Generation, Digital Analytics, Healthcare Sales, Interpersonal Relationships, Lead Generation, Lead Generation Management, Management Process, Market Analysis, Marketing Strategies, Market Intelligence, Medical Teaching, Oncology Sales, Product Knowledge, Product Marketing, Sales Account Management {+ 4 more} Preferred Skills Job Posting End Date 08/18/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R354695

Job Title : Senior Statistician Manager Location : Hyderabad Grade : L3-1 About The Job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of advanced statistical methodologies to drive manufacturing excellence and ensure product quality across our global network. Our Global Statistical Support team acts as a cornerstone to this effort. We provide critical statistical expertise to all manufacturing sites worldwide, enabling data-driven decision making and continuous improvement. Our team members serve as trusted partners to manufacturing operations, quality assurance, and process development teams, delivering statistical insights that drive operational excellence and regulatory compliance. Main Responsibilities Orchestrating a global team of statisticians to deliver consistent, high-quality statistical support across manufacturing sites while fostering professional growth and technical excellence Partnering with statisticians located on manufacturing sites to anticipate statistical support needs and proactively align resources with business priorities Establishing priorities and KPIs to measure team effectiveness and demonstrate value creation for manufacturing operations Ensuring team members are well-trained to guarantee the precision of team outputs. Able to understand the business need (potentially translated from French), drive and conduct statistical analysis interacting with people having different cultures, different backgrounds (like pharmaceutical engineers) Designing and implementing statistical control charts to monitor and optimize manufacturing and analytical/quality control processes Conducting capability studies to assess process performance and identify improvement opportunities Leading statistical comparability analyses to ensure consistency across manufacturing sites and processes, to facilitate technology transfers, and compare suppliers performances Performing stability studies using linear and non-linear modeling approaches (i.e. thermokinetic models) Supporting method validation through robust statistical design and analysis Designing and analyzing experiments (DOE) to optimize process parameters and product quality Conducting exploratory statistical analyses to support manufacturing investigations and continuous improvement Performing various data analysis (mixed-effects model, MVDA, equivalence testing…) and modeling to meet customer needs Collaborating with cross-functional teams to translate statistical insights into actionable recommendations Delivering timely, actionable statistical reports and analyses to manufacturing sites worldwide, translating complex data into clear insights that address site-specific challenges while maintaining global quality standards. Understanding Statistical SOP and train colleagues to it Understanding Protocols and customers' needs About You Experience: Experience in management and statistical analysis in pharmaceutical or manufacturing environments. Soft skills: Outstanding communication skills to convey complex statistical concepts to diverse audiences in a multicultural environment (in term of language - non-native English speakers- and background -not always related to statistics. Leadership: Inspiring and guiding a diverse team of statisticians. Stakeholder Management: Effectively engaging with cross-functional partners. Meticulous attention to detail and commitment to scientific rigor. Strong analytical mindset with the ability to propose innovative solutions. Forward-thinking with excellent anticipation of potential challenges. Methodical/organized/rigorous. Passion for standardization and harmonization of statistical approaches Technical skills: Baseline Capabilities: Proficiency in statistical software: Expert knowledge of statistical tools, programming skills on software like SAS, JMP, R, Python, or Dataiku. Statistical methodology: Strong foundation in statistical process control, experimental design, and multivariate analysis. Manufacturing knowledge: Understanding of pharmaceutical manufacturing processes and quality requirements. Regulatory knowledge: Familiarity with statistical aspects of pharmaceutical regulations and guidelines Stretch Capabilities: Understanding of relational databases and familiarity with data management tools: MS SQL Server, MySQL and Snowflake. Data visualization: Experience creating compelling visual representations of complex data using Power BI, Streamlit, etc. Familiarity with Git/GitHub for version control. Education: Master's degree in Statistics Languages: Verbal and written fluency in English , French is a bonus 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 Triomics: Triomics is focused on creating a modern technology stack for oncology trial sites and investigators. The company aims to streamline the workflows of clinical care and clinical research, bringing the healthcare industry closer to the vision of Clinical Research as a Care Option. Triomics" platform, developed in collaboration with leading cancer centers, is built on a proprietary oncology-focused large language model (OncoLLM). This platform eliminates operational inefficiencies in patient recruitment, data curation, and other laborious tasks involved in clinical research, thereby facilitating the generation of high-quality data and expediting the clinical trials. You will be part of the Oncology Clinical Team, responsible for developing Oncology Data dictionaries, Curation/Abstraction SOPs, and more. As a member of this team, you will navigate electronic medical record systems and other medical databases. Your role will involve reviewing clinical trial data to ensure consistency, completeness, and compliance with study protocols and regulatory requirements. Additionally, you will review medical records and abstract medical record data related to specified disease and project requirements. Key Responsibilities: - Screening cases for relevant clinical trials across projects and disease subtypes. - Demonstrating knowledge of cancer trials, including understanding inclusion and exclusion criteria. - Utilizing critical thinking to abstract complex concepts. - Building data libraries and collaborating with multiple departments for project-specific requirements. - Serving as an oncology subject matter expert (SME) across all cancers, with a focus on liquid cancer types. - Accessing electronic data systems to review medical records and input data accurately. - Understanding and categorizing data such as Inclusion and Exclusion criteria, adverse events, medications, etc. - Reviewing project-specific documents and familiarizing yourself with project goals and tasks. - Sharing medical and procedural knowledge with other Data Abstractors. - Responding promptly to queries from project personnel. - Performing additional duties as assigned, including eligibility assessments and QC reviews. Qualifications: - Minimum 3+ years of experience in data abstraction or patient treatment data. - Preferably, experience in oncology with a strong focus on liquid tumors. - Background in clinical research or related fields, especially oncology trials. - Advanced clinical knowledge of chronic disease states. - Certification in clinical research or clinical data management. Education: - B.Sc (Nursing), BDS, BAMS, BHMS, MDS, B.Pharm, M.Pharm Skills and Abilities: - Strong written and verbal communication skills. - Ability to make independent judgments in abstracting medical data. - Flexibility in handling changing work assignments and project requirements. - Proficiency in Microsoft Office applications. Join Triomics for the opportunity to impact and benefit patients worldwide, experience a vibrant and collaborative work culture, tackle challenging problems in a regulated industry, and collaborate with industry experts while enjoying competitive compensation.,

We are seeking a highly skilled professional with a solid academic background in biomedical sciences, surgery, or oncology to join our team. Your role will be instrumental in supporting the clinical trials of our oncology surgical equipment, ensuring compliance with regulations, and fostering scientific engagement in marketing and sales endeavors. Your responsibilities will include assisting in clinical trials, accompanying oncology surgeons in the operating room to ensure adherence to scientific and regulatory standards. You will also serve as a scientific ambassador for our products, engaging with doctors, researchers, and healthcare professionals. Collaborating with clinical teams to publish findings from trials in medical journals and conferences will be a key aspect of your role. Additionally, you will provide scientific input for marketing and sales strategies, ensuring accuracy and credibility. You will arrange and participate in medical conferences, exhibitions, and workshops to present the clinical benefits of our technology. Building and maintaining relationships with surgeons, oncologists, and research institutions for clinical collaborations will be essential. Conducting webinars, virtual demos, and training sessions for doctors and healthcare professionals will also be part of your responsibilities. The ideal candidate will hold an advanced degree (Masters or PhD) in Biomedical Engineering, Surgery, Oncology, or related fields. Experience in clinical trials, research publications, or medical device marketing is considered a plus. Strong scientific communication skills and the ability to engage effectively with healthcare professionals are crucial. A willingness to travel and participate in medical events is necessary for this role. This is a full-time position with benefits including cell phone reimbursement, Provident Fund, and a quarterly bonus. The work schedule is during the day shift, and the work location is in person.,

Skills: Social Media Strategy, Content Creation, Community Management, Brand Storytelling, Digital Campaign Management, Analytics Reporting, Reputation Management, Healthcare Marketing, Job Title: Social Media Marketing Manager Department: Marketing & Communications Location: Charni Road, Mumbai Reporting To: Head Branding & Digital Marketing / Chief Marketing Officer Experience: 58 years in social media marketing, preferably in healthcare, hospitality, FMCG, or service industries Role Objective To build, manage, and grow the hospitals social media presence across platforms by driving brand awareness, patient engagement, and reputation management. The role requires expertise in social strategy, content planning, influencer collaboration, crisis communication, and campaign execution tailored for the healthcare sector. Key Responsibilities Social Media Strategy & Planning Develop and implement a comprehensive social media strategy aligned with the hospitals brand positioning and communication goals. Identify platform-specific opportunities (Instagram, Facebook, YouTube, LinkedIn, X/Twitter, WhatsApp, etc.) for patient engagement, awareness campaigns, and live events. Content Creation & Management Collaborate with content writers, designers, doctors, and videographers to create engaging, accurate, and brand-aligned content (posts, videos, reels, infographics, etc.). Plan and maintain an editorial calendar with a mix of medical education, doctor stories, patient testimonials, awareness days, behind-the-scenes, CSR, and real-time health news. Community Engagement & Online Reputation Actively monitor and respond to comments, DMs, and queries on social channels in collaboration with the patient care or CRM team. Manage online reputation and flag/respond to reviews or negative mentions in a timely and professional manner. Drive online patient advocacy through testimonials and success stories. Campaigns & Collaborations Execute platform-specific paid and organic campaigns to support hospital departments, events, screenings, and wellness programs. Engage with medical influencers, doctors, and health bloggers for collaborations. Partner with internal departments (e.g., Oncology, Cardiology, Mother & Child) to develop targeted outreach campaigns. Analytics & Reporting Track and report social media KPIs (engagement rate, follower growth, reach, sentiment analysis, etc.). Leverage platform analytics tools and social listening tools to refine strategy and identify content trends. Conduct periodic benchmarking with peer hospitals and healthcare influencers. Compliance & Accuracy Ensure that all social content is medically accurate, approved by relevant internal stakeholders, and compliant with legal and ethical norms in healthcare communication. Coordinate with the legal and medical ethics team for approvals as needed. Key Skills & Competencies Strong command of all major social media platforms and content formats (short-form video, reels, carousels, stories, lives, etc.) Exceptional storytelling skills with a focus on emotional and ethical healthcare communication Ability to work closely with clinicians and medical staff and translate complex topics into engaging digital content Creative, agile, and up to date with digital/social trends Strong writing and copy-editing skills in English (and regional languages, if relevant) Familiarity with tools like Canva, Hootsuite, Buffer, Meta Business Suite, etc. Preferred Qualifications Bachelors or Masters degree in Marketing, Mass Communication, Digital Media, or a related field Healthcare experience preferred but not mandatory Certification in social media marketing or digital branding will be a plus

Skills: Critical Care, Patient Assessment, Ventilator Management, Infection Control, Invasive Procedures, Patient Safety, Clinical Documentation, Company Overview Sir H.N. Reliance Foundation Hospital & Research Centre, located in Mumbai, is a multi-specialty tertiary care hospital equipped with 345 beds. Committed to excellence, the hospital provides cutting-edge medical care in various thrust areas including Cardiac Sciences, Neurosciences, Oncology, and more. With a state-of-the-art Medical Mall and adhering to international standards, the institution upholds the principle of respecting life and carries forward a legacy of healthcare excellence. Job Overview We are seeking a mid-level Resident Doctor specializing in Critical Care Medicine for our Mumbai facility. This is a full-time, fixed-term employment opportunity offering a rewarding role within a technologically-advanced and compassion-driven environment. The selected individual will contribute to maintaining and enhancing our standards of patient care in a critical care setting. Qualifications And Skills MBBS/MD /DNB/IDCCM/CTCCM/DrNB Critical care /DM Roles And Responsibilities Provide expert medical care in the intensive care unit managing patients with complex and critical conditions Conduct comprehensive patient assessments and develop individualized care plans Coordinate with the healthcare team to implement effective treatment strategies Monitor patient progress and adjust treatment plans as necessary Perform essential invasive procedures such as intubations and management of central lines Ensure accurate and timely clinical documentation for all patient interactions Participate in infection control initiatives to prevent healthcare-associated infections Promote and ensure patient safety through adherence to clinical protocols and procedures

Welcome to Stemtech! As a SOLIS Specialist, you are at the heart of our mission to transform supportive oncology care. Our flagship innovation, the Eva Scalp Cooling System, helps reduce chemotherapy-induced hair loss, preserving not only hair but also confidence and dignity. Your role will directly impact patients’ lives during one of their most challenging journeys. Your Mission as a SOLIS Specialist Provide hands-on support to patients undergoing chemotherapy with the Eva Scalp Cooling System. Act as a clinical extension of the Stemtech team inside hospitals and oncology centers. Deliver empathetic, knowledgeable care while ensuring safe and effective use of the device. Core Responsibilities Patient Engagement Explain the scalp cooling process and expected outcomes. Offer emotional support during treatment sessions. Address concerns in a calm, informative, and compassionate manner. Device Operation Setup, monitor, and troubleshoot the Eva Scalp Cooling System. Maintain high standards of hygiene and equipment safety. Clinical Coordination Work collaboratively with oncology staff to integrate the Eva system into chemo workflows. Adapt to different hospital environments and protocols. Documentation & Reporting Record patient responses and treatment details accurately. Provide structured feedback to the Stemtech team on performance, usage trends, and challenges. Education & Training Assist with demos and training for nursing and hospital staff. Stay updated on protocols, device upgrades, and patient care best practices. Key Skills & Traits Empathy: Emotional intelligence and sensitivity in patient care Technical Confidence: Basic comfort with medical equipment Communication: Clear, reassuring, and respectful Attention to Detail: Accuracy in documentation and safety adherence Flexibility: Willingness to travel and work in varied clinical settings Support You Will Receive Training: Full onboarding on the Eva System, clinical protocols, and patient interaction Team Access: Continuous support from the clinical and technical teams at Stemtech Materials: Handbooks, SOPs, treatment tracking tools, and patient-facing brochures Brand Values You Represent Compassion: Because every patient matters Excellence: Because safety and outcomes are non-negotiable Innovation: Because better care is possible Closing Note As a SOLIS Specialist, you’re not just operating a device—you’re preserving dignity, reducing trauma, and restoring a sense of control for every patient you support. We’re proud to have you with us. Let’s make healing more human.

Welcome to Stemtech! As a SOLIS Specialist, you are at the heart of our mission to transform supportive oncology care. Our flagship innovation, the Eva Scalp Cooling System, helps reduce chemotherapy-induced hair loss, preserving not only hair but also confidence and dignity. Your role will directly impact patients’ lives during one of their most challenging journeys. Your Mission as a SOLIS Specialist Provide hands-on support to patients undergoing chemotherapy with the Eva Scalp Cooling System. Act as a clinical extension of the Stemtech team inside hospitals and oncology centers. Deliver empathetic, knowledgeable care while ensuring safe and effective use of the device. Core Responsibilities: Patient Engagement Explain the scalp cooling process and expected outcomes. Offer emotional support during treatment sessions. Address concerns in a calm, informative, and compassionate manner. Device Operation Setup, monitor, and troubleshoot the Eva Scalp Cooling System. Maintain high standards of hygiene and equipment safety. Clinical Coordination Work collaboratively with oncology staff to integrate the Eva system into chemo workflows. Adapt to different hospital environments and protocols. Documentation & Reporting Record patient responses and treatment details accurately. Provide structured feedback to the Stemtech team on performance, usage trends, and challenges. Education & Training Assist with demos and training for nursing and hospital staff. Stay updated on protocols, device upgrades, and patient care best practices. Key Skills & Traits Empathy: Emotional intelligence and sensitivity in patient care Technical Confidence: Basic comfort with medical equipment Communication: Clear, reassuring, and respectful Attention to Detail: Accuracy in documentation and safety adherence Flexibility: Willingness to travel and work in varied clinical settings Support You Will Receive Training: Full onboarding on the Eva System, clinical protocols, and patient interaction Team Access: Continuous support from the clinical and technical teams at Stemtech Materials: Handbooks, SOPs, treatment tracking tools, and patient-facing brochures Brand Values You Represent Compassion: Because every patient matters Excellence: Because safety and outcomes are non-negotiable Innovation: Because better care is possible Closing Note As a SOLIS Specialist, you’re not just operating a device—you’re preserving dignity, reducing trauma, and restoring a sense of control for every patient you support. We’re proud to have you with us. Let’s make healing more human.

Welcome to Stemtech! As a SOLIS Specialist, you are at the heart of our mission to transform supportive oncology care. Our flagship innovation, the Eva Scalp Cooling System, helps reduce chemotherapy-induced hair loss, preserving not only hair but also confidence and dignity. Your role will directly impact patients’ lives during one of their most challenging journeys. Your Mission as a SOLIS Specialist Provide hands-on support to patients undergoing chemotherapy with the Eva Scalp Cooling System. Act as a clinical extension of the Stemtech team inside hospitals and oncology centers. Deliver empathetic, knowledgeable care while ensuring safe and effective use of the device. Core Responsibilities Patient Engagement Explain the scalp cooling process and expected outcomes. Offer emotional support during treatment sessions. Address concerns in a calm, informative, and compassionate manner. Device Operation Setup, monitor, and troubleshoot the Eva Scalp Cooling System. Maintain high standards of hygiene and equipment safety. Clinical Coordination Work collaboratively with oncology staff to integrate the Eva system into chemo workflows. Adapt to different hospital environments and protocols. Documentation & Reporting Record patient responses and treatment details accurately. Provide structured feedback to the Stemtech team on performance, usage trends, and challenges. Education & Training Assist with demos and training for nursing and hospital staff. Stay updated on protocols, device upgrades, and patient care best practices. Key Skills & Traits Empathy: Emotional intelligence and sensitivity in patient care Technical Confidence: Basic comfort with medical equipment Communication: Clear, reassuring, and respectful Attention to Detail: Accuracy in documentation and safety adherence Flexibility: Willingness to travel and work in varied clinical settings Support You Will Receive Training: Full onboarding on the Eva System, clinical protocols, and patient interaction Team Access: Continuous support from the clinical and technical teams at Stemtech Materials: Handbooks, SOPs, treatment tracking tools, and patient-facing brochures Brand Values You Represent Compassion: Because every patient matters Excellence: Because safety and outcomes are non-negotiable Innovation: Because better care is possible Closing Note As a SOLIS Specialist, you’re not just operating a device—you’re preserving dignity, reducing trauma, and restoring a sense of control for every patient you support. We’re proud to have you with us. Let’s make healing more human.

Job title: Business Capability Manager Associate Location: Hyderabad About The Job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people in over 100 countries at Sanofi are dedicated to making a difference on patients’ daily life, wherever they live and enabling them to enjoy a healthier life. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The R&D Data Office serves as a cornerstone to this effort. Our team is responsible for cross-R&D data strategy, governance, and management. We sit in partnership with Business and Digital, and drive data needs across priority and transformative initiatives across R&D. Team members serve as advisors, leaders, and educators to colleagues and data professionals across the R&D value chain. As an integral team member, you will be responsible for defining how R&D's structured, semi-structured and unstructured data will be stored, consumed, integrated / shared and reported by different end users such as scientists, clinicians, and more. You will also be pivotal in the development of sustainable mechanisms for ensuring data are FAIR (findable, accessible, interoperable, and reusable). Position Summary The R&D Business Capability manager associate serves as the interface between Business and Digital/Data on foundational data capabilities or needs across R&D. This role will be responsible for identification of key use cases across R&D, high level data solutioning (e.g., data strategy, governance/standards, management, infrastructure needs etc), and oversight of day-to-day operations for their specific data capability. Main Responsibilities Work in collaboration with R&D Data Office leadership, business, and R&D Digital subject matter experts: Partner with key stakeholders across R&D functions to identify data-related needs and initiatives (e.g., data catalog, master and reference data management, data products, etc.) and design innovative data solutions to support business prioritiesPartner with R&D Digital stakeholders to oversee data-related activities and verify data functionality from ingest through access Drive program management of initiatives and capabilities; ensure on-schedule/on-time delivery and proactive management of risks/issues Establish ways of working across all partner functions for specifically assigned capabilities/initiatives Annotate genomic variants (e.g., SNVs, indels, CNVs, SVs) using open source or proprietary tools on relevant databases to assess functional and clinical relevance Integrate genomic annotations with pathway databases, transcriptomic data, and disease ontologies to generate hypotheses about target biology and mechanism of action Work with multi-omics data sets (e.g., WES, WGS, RNA-seq, scRNA-seq) and curate data pipelines to ensure quality, consistency, and reproducibility of annotations Partner with wet-lab scientists, data scientists, and therapeutic area teams to deliver actionable insights for target validation, biomarker discovery, and patient stratification Contribute to the development and maintenance of automated workflows, reproducible pipelines and databases Document methodologies and present results in internal meetings, reports, and collaborative discussions with cross-functional stakeholders Deliverables Develops business case development, requirement identification, and use case development for business functions Implements business process definition, process performance, process execution, process management, and continuous improvement opportunities Maintain genomic databases, pipelines, tools and platforms undefined About You Experience: M.S + 5 years or Ph.D. +3 years hands-on experience in bioinformatics, preferably in a pharma, biotech, or translational research setting Proficient in scripting languages (e.g., Python, R, Bash) and bioinformatics tools for genomic annotation Solid understanding of human genetics, disease biology, and functional genomics data sets Familiarity with ontologies and biological knowledgebases (e.g., GO, KEGG, Reactome, DisGeNET) Experience working with NGS data and variant interpretation in the context of drug discovery or precision medicine Experience with workflow languages (e.g., Nextflow, Snakemake, WDL), Knowledge of clinical genomics standards (e.g., HGVS nomenclature, ACMG classification) Familiarity with target identification and validation pipelines or biomarker discovery programs Familiarity with Pharma R&D processes and technology, Ability to build business relationships and understand end-to-end data use and needs Diplomatic and stakeholder management skills across business, technology, and partners Demonstrated strong attention to detail, quality, time management and customer focus Excellent written and oral communications skills, Strong networking, influencing and negotiating skills and superior problem-solving skills Demonstrated willingness to make decisions and to take responsibility for such, Excellent interpersonal skills (team player) People management skills either in matrix or direct line function, M.S. or Ph.D. in Bioinformatics, Computational Biology, Genomics, or a related discipline 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.

Job Category Job Type: Job Location: Salary Years of Experience: Downstream Product Manager Precision Oncology & Spatial Biology Location: Adibatla, Hyderabad, India | Full-Time | Commercial Strategy Role Benefits Competitive Salary Performance Incentives Health Benefits Generous PTO At OmicsVeu, were transforming precision oncology through cutting-edge innovations in molecular pathology, spatial biology, and spatial transcriptomics. As we expand our global footprint, were looking for a strategically minded and execution-driven Downstream Product Manager to drive the success of our commercial-stage product lines. This role is ideal for someone with strong life sciences expertise, a commercial mindset, and a digital marketing-driven approachready to turn scientific innovation into market success and enable cross-functional teams to thrive. Your Key Responsibilities Develop and execute downstream marketing strategies for launched products. Define competitive positioning, core messaging, and differentiated value propositions. Lead the development of pricing strategies, market segmentation, and customer targeting plans. Design and deliver training programs for internal sales teams, field application specialists, and customers. Create high-impact marketing collateralincluding presentations, brochures, case studies, product guides, and digital content. Equip the commercial team with battle cards, objection-handling tools, and sales enablement kits. Capture and analyze voice-of-customer insights through direct engagement with clients, KOLs, and partners. Collaborate closely with Sales, R&D, Product Development, and Clinical Affairs to align strategy and execution.

Job title: Expert Quality Services (Product Complaints) Location: Hyderabad About The Job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people in over 100 countries at Sanofi are dedicated to making a difference on patients’ daily life, wherever they live and enabling them to enjoy a healthier life. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting Global M&S teams in partnership with Business and Digital, and drive priority and transformative initiatives across M&S. The team members of Global M&S Services Hubs will act as partners in carrying out tasks and fulfilling responsibilities to support identified and established global quality processes from the hubs. Main Responsibilities Handle Product Technical Complaints and Field Alerts for medical devices, pharmaceutical products, biologics, and combination products, ensuring compliance with regulatory standards. Manage the entire process of handling Product Technical Complaints and Field Alerts from receipt to closure, ensuring compliance with internal procedures and regulatory requirements. Collaborate with internal and external manufacturing sites, Customer Service, Medical Information, Pharmacovigilance, Sales Associates, Regulatory, Commercial Operations, Legal, and Risk Management departments. Evaluate complaints for severity and risk, ensuring timely review and processing. Prioritize and enter complaints into the global database, monitoring complaint activity for assigned manufacturing sites. Produce monthly reports for manufacturing sites on complaint activity and support during audits and regulatory inspections. Participate in ad-hoc teams for product-specific complaint issues and provide feedback on complaint investigations. Focus on operational tasks within the compliant handling process. Identify and implement continuous improvement opportunities. Provide regulatory interpretation and guidance to internal teams. Manage and oversee the training within the department. Perform quality checks on PQC activities, prepare reports, and maintain inspection readiness. About You Experience: 6 – 10 years of related experience in the pharmaceutical industry. Knowledge of cGMP’s, Code of Federal Regulations in drugs and biologics, and complaint database software and reporting tools. Should be knowledgeable in Quality functions of pharmaceutical industry. Experience of working on manufacturing sites is an added advantage. Proficient in problem-solving, attention to detail, and good organizational skills. Work in a team-oriented, flexible, and proactive manner. Analytical skills and ability to multitask in a stressful environment. Education: Bachelor’s or Masters in Life Sciences/Healthcare, Business Administration, Engineering or Information Technology. Languages: Verbal and written fluency in English Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks’ gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas. 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.

Job description Job role Details: (Just same as a Medical Representative) The ethical promotion of Nestle's infant nutrition products in their territory by clearly communicating with Health Care Professionals (HCPs) about Nestle's Infant Nutrition products, their features, advantages, benefits and their appropriate use, within the Code of Ethics Nestle's instructions and keeping in mind, mother's milk is best for Babies. Ensuring recommendation for the Nestle Nutrition product range within the scope of the Indian Code, detailing against homemade Paps and bovine milk. Being a reliable source of information on infant nutrition and infant feeding practices. Ensuring quality execution in terms of detailing/ conducting scientific symposiums etc. as per the company guidelines. Who can apply: Candidates who are graduates with at least 1 year of experience in nutrition or pharmaceutical industry. Candidates with high level of integrity & honesty, hardworking, self-motivator and passionate about enhancing quality of life and contributing to healthier future. Being able to work effectively in a team Ability to build strong and sustainable relationships High Learning agility Trustworthy and be able to work independently within the company policy & guidelines Nestle is committed to providing equal opportunities without any discrimination on the grounds of age, color, disability, origin, nationality, religion, race, gender, or sexual orientation. We are an equal opportunity employer, and we value diversity at our company. For any reasonable accommodation in the recruitment process for persons with disabilities, kindly reach out to your recruiter. Reasonable accommodation includes any appropriate modifications to ensure that persons with disabilities are provided an equal platform in the recruitment process's s

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 Associate Software Engineer What You Will Do Let’s do this. Let’s change the world. In this vital role you will be responsible for developing and maintaining Salesforce applications to meet business needs. You will collaborate with a team of software engineers, participate in the full software development process, and ensure the delivery of high-quality code and solutions. Your strong programming skills, problem-solving abilities, and attention to detail will contribute to the development of robust and scalable software solutions. Roles & Responsibilities: Design and implement Salesforce Lightning components using LWC and Aura frameworks to enhance platform functionality and user experience. Configure roles, profiles, permission sets, and region-wise security and sharing settings to ensure appropriate access control across user groups. Create and customize standard and custom objects, page layouts, validation rules, record types, and formula fields to meet business requirements. Develop and maintain Apex classes, triggers, Visualforce pages, and custom controllers as needed. Design and implement integrations between Salesforce and external/internal systems using REST/SOAP APIs and middleware. Use Copado to manage source control, deployments, pipeline automation, and environment management in support of release processes Apply Salesforce development standard processes to ensure code reusability, maintainability, and compliance with performance and scalability standards. Collaborate with quality and validation teams to develop test scripts and implement functional and system testing in regulated environments. Fix and resolve development or configuration issues during QA, UAT, and production support cycles. Participated in design reviews, sprint planning, and code reviews, contributing to Agile/Scrum ceremonies and delivery cycles. Maintain documentation including technical design, solution architecture, and release notes for enhancements and projects. Ensure all development work adheres to GxP, CSV, and compliance requirements, including documentation traceability and audit readiness. Collaborate with business analysts, QA, validation, and infrastructure teams to deliver reliable and compliant Salesforce solutions. Stay up to date with Salesforce platform releases, new features, and emerging technologies to drive innovation and platform optimization. What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. Master's degree / Bachelor's degree and 5 to 9 years of Computer Science, IT or related field experience Preferred Qualifications: BS/MS in Computer Science, Information Technology, or a related technical field 4+ years of experience in Salesforce development including Lightning Components, Apex, Visualforce, and platform configuration Hands-on experience with Salesforce security models, role hierarchy, sharing rules, and field-level access Solid hands-on experience of implementing Salesforce Configurations, Apex, LWC, Aura Solid understanding of Salesforce object model, workflows, validation rules, and triggers Experience with Salesforce integrations using RESTful and SOAP web services Familiarity with DevOps practices, CI/CD tools, and version control systems like Git Demonstrable experience working with Copado for deployment automation, CI/CD pipeline configuration, and release management Strong problem-solving skills and the ability to solve issues across multiple environments Experience working in Agile/Scrum teams supporting enterprise applications Salesforce platform certifications are a strong plus Must-Have Skills: Proficient in developing custom solutions using Salesforce Lightning Components (Aura and LWC), Apex classes, Visualforce pages, and Apex triggers, including batch classes and schedulers with exception handling. Experience configuring standard/custom objects, fields, page layouts, validation rules, roles, profiles, permission sets, and region-specific sharing and access models. Hands-on experience integrating Salesforce with internal and external systems using REST and SOAP APIs; familiarity with middleware for system interoperability. Familiarity with DevOps tools, version control systems (e.g., Git), and CI/CD pipelines beyond Copado, contributing to efficient and traceable deployments. Strong analytical attitude with the ability to fix platform issues, optimize performance, and explore emerging Salesforce features for continuous improvement. Good-to-Have Skills: Skilled in using Copado for deployment automation, CI/CD pipeline configuration, source control management, and environment management across multiple sandboxes. Experience participating in Agile/Scrum teams, with knowledge of sprint planning, retrospectives, and iterative development workflows. Deep understanding of Salesforce object model, workflows, formula fields, and Apex triggers customizing and extend platform functionality. Exposure to pharmaceutical, biotech, or healthcare industries with an understanding of compliance and patient safety requirements. Professional Certifications Salesforce Platform Developer I (required) Salesforce Platform Developer II (preferred) Salesforce Administrator Certification (plus) Certified Scrum Developer or SAFe Agile (optional) Certified CSV or Validation Professional (optional) Soft Skills: Excellent problem-solving and analytical skills Good communication and interpersonal abilities High attention to detail and commitment to quality Ability to prioritize tasks and work under stress Team-oriented with a proactive and collaborative approach Willingness to mentor junior developers and promote standard methodologies Adaptable to changing project requirements and evolving technology 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.

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. IS Organizational Effectiveness Manager – Scrum Master HR Product Teams What You Will Do Let’s do this. Let’s change the world. In this vital role you will lead and coach who facilitates team events, processes, and supports teams in delivering value within the Hire to Retire capability. The role involves facilitating communication and collaboration among teams, ensuring alignment with the program vision, managing risks and dependencies, and driving relentless improvement. They also often participate in the Lean-Agile transformation, coaching leaders, teams, and Scrum Master/Team Coaches in the new mindset and processes. They help adapt SAFe to the organization’s needs, standardizing and documenting practices. Roles & Responsibilities: Lead and manage product delivery using agile frameworks and techniques. Align with Agile values such as prioritizing individuals and interactions over processes and tools. Lead and facilitate agile events including stand-ups, sprint/PI planning, sprint/PI reviews, retrospectives, demos and backlog refinement meetings to promote team collaboration. Advise SAFe events, including PI Planning, Scrum of Scrums, and Inspect & Adapt workshops. Collaborate with cross-functional teams to identify business requirements and develop solutions that meet customer needs. Work with Product Owners, Product and Solution Management, and collaborators to ensure strategy and execution alignment Help the scrum teams achieve delivery acceleration focused on business outcomes by reaching higher levels of scrum maturity Identify, escalate, and manage risks and dependencies across Teams to ensure that they are addressed in a timely manner Coordinate with Services and support to schedule resolution of issues with released products Foster a culture of continuous improvement within the Teams by leading retrospectives and encouraging innovation Monitor and report on the progress of the Team, ensuring transparency and alignment with solution objectives What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Master’s degree with 4 - 6 years of experience in Computer Science, Business, Engineering, IT or related field OR Bachelor’s degree with 6 - 8 years of experience in Computer Science, Business, Engineering, IT or related field OR Diploma with 10 - 12 years of experience in Computer Science, Business, Engineering, IT or related field Strong understanding of Agile methodologies, particularly the Scaled Agile Framework (SAFe) Prior experience with Agile project management tools, such as Jira, Confluence and Jira Align Experience in guiding teams through Agile events and ensuring adherence to SAFe practices and behaviors Excellent problem-solving skills and a passion for tackling complex challenges with data Collaborative spirit and effective communication skills to work seamlessly in a cross-functional team Preferred Qualifications: Deep understanding of DevOps and Test Automation Processes in software delivery Workshop facilitation and training experience Certified SAFe Scrum Master or similar (preferred) Experience working within the Hire to Retire or Human Resources function Soft Skills: Excellent people and project management skills Ability to work collaboratively with cross-functional teams Ability to manage 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.

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. Associate IS Engineer - Clinical Trial Registry System What You Will Do As an Associate IS Engineer at Amgen, you will be responsible for managing, designing and implementing information system architectures to support business needs. You will interact with business owner and teams to analyze requirements, develop architectural designs, evaluate technology solutions, perform relevant validation and ensure alignment with industry best practices and standards. Your expertise in system architecture, strong problem-solving abilities, and ability to communicate complex technical concepts will enable you to deliver robust and scalable IT solutions. Collaborate with business and data stakeholders to gather requirements, assess data needs, and ensure data quality, privacy, and compliance across ETL pipelines. Develop, monitor, and maintain CI/ CD-enabled ETL pipelines using Databricks and AWS services (S3, Glue, Lambda, EMR, etc.). Optimize ETL jobs for performance, scalability, cost-efficiency, and data quality using standard processes for data ingestion, transformation, and loading. Identify, fix, and resolve pipeline bottlenecks or failures to maintain data pipeline health. Maintain user documentation for data definitions, flows, lineage, and quality rules to support audit readiness and data governance. Ensure alignment to data governance policies and contribute to improvement initiatives around data standardization and harmonization. Engage in Agile/SAFe ceremonies, provide story estimates, and deliver user stories related to data platform enhancements. Participate in sprint planning meetings and provide estimations on technical implementation Work with data engineers on data quality assessment, data cleansing and data analytics. Share and discuss findings with team members practicing SAFe Agile delivery model. Automate and Optimize data pipeline and framework for easier and cost-effective development process. Assist in driving validation and compliance readiness by overseeing the development of validation plans, IQ/OQ/PQ protocols, and related documentation as per GXP, 21 CFR Part 11, and Annex 11 guidelines. Oversee user access controls, role-based privileges, and audit trail configurations to ensure system integrity and security are maintained. Support the change control process for the submission system by aligning with ITIL standards and ensuring traceability for all updates, patches, and configuration changes. Use Jira and ServiceNow for project tracking, issue resolution, and service management. What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. The professional we seek is with these qualifications. Basic Qualifications: Bachelor’s degree and 2 to 6 years of relevant experience Must-Have Skills: Ability to analyze and interpret complex data to identify and remediate issues Sharp learning agility, problem-solving and analytical thinking Scripting skills such as PowerShell or Python Strong knowledge of Data Lake technologies like Databricks, etc. Experience in MuleSoft, Python script and REST/RESTful API script development. Experience in Clinical system integration. Good written and verbal communication skills Experience working in agile methodology, including Product Teams and Product Development models leading Scrum teams using Jira and Confluence, and adopting Agile methodologies like Kanban and Lean for product development. Proficiency in designing scalable, secure, and cost-effective solutions like cost optimization using AWS Cost Explorer. Have stakeholder and team management skills. Could lead and guide multiple teams to meet business needs and goals. Good-to-Have Skills: Experience with IS Security Experience with Agile Project Methodology Familiarity with cloud platforms (e.g., AWS, Azure, Google Cloud) and their IAM services. Knowledge of IGA principles, including role-based access control (RBAC) Knowledge of incident response procedures and the ability to manage security incidents related to identity management Professional Certifications: Microsoft, GCP or AWS Cloud (preferred) Security Certification (preferred) Microsoft Azure Certification (preferred) Soft Skills: Analytical and troubleshooting skills Good verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Ability to manage 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.