1112 Pharmacology Jobs - Page 24

Job Title: Cardiologist Location: Patna, Bihar Job Type: Full-time Department: Cardiology Reports To: Head of Cardiology / Medical Superintendent Salary: 3,00,000/- to 4,00,000/- Per Month . Job Description: About the Role: We’re looking for a passionate and skilled Cardiologist to join our team in delivering high-quality heart care. If you're committed to combining clinical precision with a human touch, and thrive in a collaborative, patient-focused environment, we’d love to hear from you. Key Responsibilities: · Diagnose and treat heart conditions including coronary artery disease , heart failure , arrhythmias , valvular disease , and hypertension . · Perform and interpret ECGs , echocardiograms , TMT , Holter monitoring , and cardiac catheterizations . · Offer personalized treatment plans , including medications , lifestyle counselling , and interventional procedures . · Manage emergency cardiac care and collaborate with ICU, surgery, and general medicine teams. · Maintain detailed medical records, follow NABH protocols , and communicate clearly with patients and families. Essential Skills & Expertise: · Solid understanding of cardiac anatomy, physiology, and pathology · Skilled in interpreting diagnostic tools like ECGs , echo , CT , MRI , and conducting cardiac cath · Experienced in medication management and offering lifestyle modifications for long-term cardiac care · Trained in interventional cardiology — angioplasty , stenting , pacemaker implantation · Knowledge of electrophysiology and rhythm disorder management · Strong grasp of the pharmacology of cardiac drugs · Team-oriented with excellent patient communication and follow-up care Qualifications: MBBS + MD (Medicine) + DM / DNB (Cardiology) At least 3+ years experience. MCI or State Medical Council registration Training in intervention or electrophysiology is a plus ACLS/BLS certified (preferred) To Apply: Send your resume and a short cover letter to hr.himalayagroup1@gmail.com/hr@himalayagroupofinstitutions.com or contact over Whatsapp:9031624659/9031624657. Job Types: Full-time, Permanent Pay: ₹300,000.00 - ₹400,000.00 per year Schedule: Day shift Morning shift Work Location: In person

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - RA / SRA (S1/S2/S3/S4) Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-8y in analytical chemistry (HPLC/LCMS/NMR or purification) Interaction with synthetic team and problem solving skills. Should be able to handle the respective instrument Knowledge of instrumental technique with its application Should be able to handle routine analysis independently on respective instrument. Experience in method development on HPLC/LCMS will be desirable but not necessary Maintenance, cleaning, documentation and calibration of analytical instruments. Maintain laboratory as safe working place. Person Profile Qualification: - M. Sc (Analytical Chemistry) Experience: - 2 years of relevant experience Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Capital Hospitals is looking for Sr.Pharmacist to join our dynamic team and embark on a rewarding career journey Dispense prescriptions and counsel patients on medications Supervise pharmacy staff and ensure inventory control Maintain compliance with drug laws and protocols Collaborate with doctors for accurate medication usage

Urgent Requirement for Assistant Professor-Pharmacology with 1 to 3 yrs experience

Graduation, life science background preferably Physiotherapist, Pharma, Nursing, Biochemistry and Microbiology CPC or equivalent valid coding certification Minimum of 2 year performing CPT E/M and ICD 10 coding for academic facilityStrong human anatomy/physiology knowledgeShould have good reading comprehension & abstraction skillsWilling to work for Rotational shifts Work from office only Accurately code physician practitioner services through review of medical record documentation and encounter forms Assign CPT procedure codes, ICD-10 diagnosis codes, and modifiers based on documentation, government teaching physician documentation requirements and LCD/NCD/NCCI policies Working knowledge of E/M (Inpatient & Outpatient setting), CPT coding - Medicare 1995/1997 Documentation Guidelines Convert document into numeric format \ Enter Logs Should be aware of entire E/M section (All range of E/M codes) Should have knowledge of minor CPT codes along with E/MShould know to handle trauma charts as well Should be aware of all E/M modifiers Excellence in ICD10-CM and CPT coding principles and guidelines Knowledge of medical terminology, abbreviations, techniques, and surgical procedures; anatomy and physiology; major disease processes; pharmacology

Job Title: MD Pharmacology Doctor Company: Seva At Home 📍Location: Sector 62, Gurugram ⏳Duty Hours: 10 AM - 7 PM IST Working Days: Monday - Friday 💰 Salary Upto 2 lakh per month. Type: Full-time (URGENT Requirement) Job Summary : Seva At Home is seeking an experienced and highly motivated MBBS + MD Pharmacology professional to join our core team. The ideal candidate will play a crucial role in standardizing pharmacy processes, ensuring compliance with medical protocols, implementing evidence-based practices, and contributing to product research and development. This is an urgent requirement for a dedicated individual committed to enhancing healthcare services and compliance. Key Responsibilities : Serve as a Medical/Subject matter expert within the core team. Standardize and optimize Pharmacy processes. Conduct quality checks of existing procedures to ensure high standards. Implement evidence-based practices in all relevant operations. Ensure strict compliance with all medical and operational protocols. Conduct research and provide feedback for new products before their inclusion in inventory. Provide regular feedback on current products and outline future directions to enhance compliance and services. As part of due diligence, meticulously proofread all significant legal clinical documents. Requirements : MBBS and MD in Pharmacology is mandatory. 3-5 years of relevant professional experience in pharmacy business. Strong understanding of medical protocols and pharmaceutical processes. Ability to implement and ensure compliance with established guidelines. Excellent research and analytical skills. Attention to detail, particularly in document review. Strong communication and teamwork skills. Ready to take the leap? Send your CV to Mr.Vicky Kumar vicky.kumar@sevaathome.com 093119 63641

Job Description Jr. Analytics Engineer We are seeking a talented, motivated and self-driven professional to join the HH Digital, Data & Analytics (HHDDA) organization and play an active role in Human Health transformation journey to become the premier “Data First” commercial biopharma organization. As a Analytics Engineer, you will be part of the HHDDA Commercial Data Solutions team, providing technical/data expertise development of analytical data products to enable data science & analytics use cases. In this role, you will create and maintain data assets/domains used in the commercial/marketing analytics space – to develop best-in-class data pipelines and products, working closely with data product owners to translate data product requirements and user stories into development activities throughout all phases of design, planning, execution, testing, deployment and delivery. Your specific responsibilities will include Hands-on development of last-mile data products using the most up-to-date technologies and software / data / DevOps engineering practices Enable data science & analytics teams to drive data modeling and feature engineering activities aligned with business questions and utilizing datasets in an optimal way Develop deep domain expertise and business acumen to ensure that all specificalities and pitfalls of data sources are accounted for Build data products based on automated data models, aligned with use case requirements, and advise data scientists, analysts and visualization developers on how to use these data models Develop analytical data products for reusability, governance and compliance by design Align with organization strategy and implement semantic layer for analytics data products Support data stewards and other engineers in maintaining data catalogs, data quality measures and governance frameworks Education B.Tech / B.S., M.Tech / M.S. or PhD in Engineering, Computer Science, Engineering, Pharmaceuticals, Healthcare, Data Science, Business, or related field Required Experience 3+ years of relevant work experience in the pharmaceutical/life sciences industry, with demonstrated hands-on experience in analyzing, modeling and extracting insights from commercial/marketing analytics datasets (specifically, real-world datasets) High proficiency in SQL, Python and AWS Good understanding and comprehension of the requirements provided by Data Product Owner and Lead Analytics Engineer Experience creating / adopting data models to meet requirements from Marketing, Data Science, Visualization stakeholders Experience with including feature engineering Experience with cloud-based (AWS / GCP / Azure) data management platforms and typical storage/compute services (Databricks, Snowflake, Redshift, etc.) Experience with modern data stack tools such as Matillion, Starburst, ThoughtSpot and low-code tools (e.g. Dataiku) Excellent interpersonal and communication skills, with the ability to quickly establish productive working relationships with a variety of stakeholders Experience in analytics use cases of pharmaceutical products and vaccines Experience in market analytics and related use cases Preferred Experience Experience in analytics use cases focused on informing marketing strategies and commercial execution of pharmaceutical products and vaccines Experience with Agile ways of working, leading or working as part of scrum teams Certifications in AWS and/or modern data technologies Knowledge of the commercial/marketing analytics data landscape and key data sources/vendors Experience in building data models for data science and visualization/reporting products, in collaboration with data scientists, report developers and business stakeholders Experience with data visualization technologies (e.g, PowerBI) Who We Are … We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world. What We Look For … Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. 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 Hybrid Shift Valid Driving License Hazardous Material(s) Required Skills Amazon Web Services (AWS), Applied Engineering, Biopharmaceutical Industry, Biopharmaceutics, Business Intelligence (BI), Computer Science, Data Management, Data Modeling, Data Science, Data Visualization, DevOps Engineering, Healthcare Innovation, Hospital Medicine, Management Process, Measurement Analysis, Pharmacology, Pharmacotherapy, Social Collaboration, Stakeholder Relationship Management, Statistical Data Modeling, Waterfall Model Preferred Skills Job Posting End Date 06/24/2025 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 R354943

This role is for one of our clients Industry: Hospitals and Health Care Seniority level: Associate level Min Experience: 0 years JobType: full-time About the Opportunity We are seeking a dedicated and detail-oriented Consultant Anesthesiologist to join a leading multi-specialty hospital in Bhavnagar. This opportunity is ideal for early-career medical professionals looking to build a long-term career in a technologically advanced, patient-centric clinical environment. You will play a vital role in delivering safe, effective anesthesia care across a broad range of surgical specialties, working alongside some of the region’s most skilled medical teams. If you are committed to clinical excellence, collaborative teamwork, and continuous learning, this role offers the ideal platform to grow and make a meaningful impact. Key Responsibilities Anesthesia Delivery & Patient Monitoring Administer general, regional, and local anesthesia for surgical, diagnostic, and therapeutic procedures. Continuously monitor patient vitals and anesthetic depth to ensure intraoperative safety and stability. Tailor anesthesia techniques to suit individual patient conditions, comorbidities, and procedural requirements. Preoperative & Postoperative Patient Management Conduct thorough pre-anesthetic evaluations including risk assessment and patient counseling. Manage postoperative recovery, pain control protocols, and potential anesthesia-related complications. Maintain clear communication with patients and families about anesthesia procedures and expectations. Interdisciplinary Collaboration Work closely with surgeons, intensivists, physicians, and nursing staff to provide seamless perioperative care. Participate in pre-surgical briefings, case reviews, and critical care planning for high-risk patients. Documentation & Compliance Maintain accurate and comprehensive medical records of all anesthesia interventions and observations. Ensure adherence to institutional policies, safety standards, and national medical guidelines. Mentorship & Clinical Learning Supervise and support residents, fellows, and medical interns during procedures. Demonstrate the correct use of monitoring and anesthesia equipment, emphasizing patient safety and efficiency. Professional Growth & Contribution Engage in hospital-led clinical audits, quality assurance activities, and department meetings. Stay abreast of the latest research, protocols, and technologies in anesthesiology through CME programs and medical conferences. Candidate Profile Qualifications: MD / DNB in Anesthesiology from a recognized medical institution. Must hold valid registration with MCI or relevant State Medical Council. Experience: 0–3 years of post-qualification experience (Freshers encouraged to apply). Core Competencies: Strong foundation in pharmacology, physiology, and anesthesia techniques. Confidence in handling emergencies and making critical intraoperative decisions. Clear and empathetic communication skills with both patients and medical teams. Strong commitment to patient care, ethical practice, and continuous improvement. Why Join Us? Be part of a highly reputed multi-specialty hospital with advanced infrastructure. Learn and grow under the mentorship of seasoned medical professionals. Enjoy a collaborative work environment that values compassion, innovation, and clinical integrity. Competitive compensation package with opportunities for academic contribution and skill enhancement.

Key Responsibilities: Dispensing Medications: Accurately review and fill prescriptions. Ensure compliance with legal and ethical standards in dispensing medicines. Patient Counseling: Provide clear instructions on medication usage, potential side effects, and interactions. Advise patients on the management of their health and wellness. Medication Management: Oversee and manage stock levels to ensure the availability of essential drugs. Maintain records of all prescriptions and inventory. Collaboration: Work closely with doctors, nurses, and other healthcare professionals to ensure optimal patient care. Offer expertise on drug selection, dosage, and potential interactions. Regulatory Compliance: Stay updated on pharmaceutical regulations and guidelines. Ensure proper labeling and storage of medications. Education and Awareness: Provide information about vaccinations and health screenings. Educate patients and communities about preventive healthcare measures. Research and Development (Optional): Contribute to research on new medications or healthcare products. Participate in clinical trials, if applicable. Skills and Qualifications: Educational Requirements: Bachelor’s or Doctorate degree in Pharmacy (B.Pharm or Pharm.D). ONLY MALE STAFF PERFERABLE FRESHERS CAN ALSO APPLY Licensure: Valid pharmacy license as per local regulations. Technical Skills: Proficiency in pharmaceutical software and tools. Soft Skills: Excellent communication, attention to detail, and problem-solving abilities. Knowledge Base: In-depth understanding of pharmacology, drug interactions, and medical terminology. Job Type: Full-time Pay: ₹10,000.00 - ₹15,000.00 per month Schedule: Day shift Education: Diploma (Preferred) Work Location: In person

You get to collaborate on Medicinal Chemistry of Lead Generation and Lead Optimization of Pipeline Projects. Understand Structure Activity Relationships and Structure Property Relationships of various projects. Collaborate with Medicinal Chemistry, Pharmacology, Analytical, ADME, Tox, IP, Site and Global Leadership. Develop appropriate flow schemes with relevant in vitro, in vivo, ADME/PK and tox studies. Appropriate allocation of resources for maximum cost effectiveness. Work effectively with Project ManagementMake presentations of your projects at various Enveda forums. You work with the site safety head and emphasize the importance of safe practices in the chemistry laboratories Who will thrive in this role Doctor of Philosophy in Synthetic Organic Chemistry15-20 years of post-PhD experience in Medicinal Chemistry Proven track record of delivery of leads and clinical candidates to the pharmaceutical industry. Management and mentoring of synthetic chemists. Good understanding of intellectual property of medicinally valuable compounds with respect to composition of matter, method of use and chemical processes. Strong understanding of safety practices in organic synthesis laboratories. If you don't meet all of the requirements listed here, we still encourage you to apply. No job description is perfect, and we might find an even more suitable opportunity that matches your experience.

Roles & Responsibilities: Responsible for serving as a core scientific member of the cross-functional franchise team, providing the scientific foundation for the Therapeutic Area (TA) medical strategy. Responsible for conceptualizing and managing a wide range of medical activities, aligned with the TA Medical strategy, including research, publications, medical education, and patient support programs. Engaging key thought leaders through medical affairs activities, in line with the overall strategic plan. Ensuring the optimal execution of the strategic medical affairs plan through Regional Medical Affairs, encompassing medical education, product education, and special projects. Acting as a therapeutic area scientific expert, discussing scientific data with leading specialists, and providing training on the latest medical developments to the sales and marketing team. Candidate Profile: M.D. Pharmacology with 2-4 years of experience in the pharmaceutical industry or research company. Knowledge of drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines Excellent Communication skills, both written and verbal (including medical writing and presentation skills) Analytical skills and reasoning, and sound medical judgment/decision making Interpersonal skills, internal & external networking and the ability to impact and influence Comfortable to travel

Job Title: Study Monitor Support Specialist Introduction to role: Are you ready to dive into the world of non-clinical study monitoring? As a Study Monitor Support Specialist, you'll play a pivotal role in supporting the Study Monitor group within Regulatory Toxicology and Safety Pharmacology. Your contributions will be vital in ensuring the smooth execution of studies that pave the way for groundbreaking medical advancements. Accountabilities: Support the study monitoring of in vitro safety pharmacology (hERG) studies. Assist NonClinical Toxicology Study Monitors with key study activities. Provide essential support for external study monitor activities. Maintain and update supporting documents. Identify and implement effective toxicology study processes to enhance efficiency and simplify operations. Continuously evaluate the end-to-end process for CRO study management to identify weaknesses and gaps, focusing on improvement and simplification. Manage financial aspects of study conduct, including approval and review of Statements Of Work, Invoices, and Purchase Orders. Maintain a tracker for ongoing study costs. Support ad hoc requests for metrics and information gathering activities. Perform QC checks of submission documents. Essential Skills/Experience: Fluent in English (spoken and written). Experience working in a GLP Toxicology lab with an understanding of practices, principles, and concepts associated with planning and delivering non-clinical toxicology studies. Ideally, experience relevant to the delivery of in vitro electrophysiology assays measuring activity at cardiac ion channels (including hERG). Ideally BSc in Pharmacology / Toxicology. Experience delivering to multiple concurrent projects, with the ability to take ownership. Strong stakeholder management skills with excellent communication skills. Experience in improvement projects with a drive to ensure efficient ways of working. A dedicated team player with excellent communication and influencing skills, experienced in working in multidisciplinary matrix teams across various geographical locations. Results-oriented with high scientific standards combined with a delivery focus to support project execution. Proficient in the use of Microsoft Office products. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, we are driven by curiosity and courage, constantly exploring new scientific frontiers to tackle some of the world's most complex diseases. Our commitment to making a difference is unwavering as we fuse data and technology with scientific innovation to achieve breakthroughs that impact billions of lives globally. Here, you will find an inclusive environment where collaboration thrives, empowering you to make bold decisions and celebrate successes along the way. With opportunities for lifelong learning and career growth, AstraZeneca is where you can truly make an impact. Ready to take on this exciting challenge? Apply now and be part of our journey to redefine what's possible in healthcare!

About Eurofins: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is a global leader in food, environmental, pharmaceutical and cosmetic product testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a network of over 1,000 independent companies in 54 countries, operating 900 laboratories. Performing over 450 million tests every year, Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. Eurofins is one of the fastest growing listed European companies with a listing on the French stock exchange since 1997. In FY 2021, Eurofins achieved a record revenue of over EUR 6.7 billion. Eurofins IT Solutions India Pvt Ltd (EITSI) is a fully owned subsidiary of Eurofins and functions as a Global Software Delivery Center exclusively catering to Eurofins Global IT business needs. The code shipped out of EITSI impacts the global network of Eurofins labs and services. The primary focus at EITSI is to develop the next generation LIMS (Lab Information Management system), Customer portals, e-commerce solutions, ERP/CRM system, Mobile Apps & other B2B platforms for various Eurofins Laboratories and businesses. Young and dynamic, we have a rich culture and we offer fulfilling careers. Job Description Role: Support Engineer Department: Information Technology Levels: II Status: Full Time/Exempt Location: Corporate Manages Others: No Basic Function and Scope of Responsibility: The Support Engineer role is primarily responsible to provide a single point of contact for end users to receive support within the organization's desktop computing environment. This includes installing, diagnosing, repairing, maintaining, and upgrading all end-user equipment to ensure optimal performance. The person will also provide frontline help desk coverage (in person, by telephone, or via email), requiring problem analysis, technical assistance, and training of associates for various information systems. Essential Job Duties: Level I - Minimum Answer help desk tickets and provide remote support by troubleshooting and resolving hardware, software, printer, connections, phone and messaging systems issues. Provide the first level of support for all technical issues. Provide triage service for all incidents, including first response, information gathering, and routing incidents to appropriate teams. Provide desktop support for incidents that cannot be resolved remotely. Maintain complete, timely, and accurate records of support in the ticketing system, including knowledge base updates to assist others in resolving similar tickets. Assist employees with general administrative needs relating to passwords, application access, local backups/restores, forms, and policies. Educate end users on operating systems and software applications and how to use the phone system effectively. Set up computer, equipment, phone, email, voicemail, and security for new users. Make any changes or deletions for employee moves or terminations. Participate in training new employees at new hire orientations. Manage user accounts and permissions. Maintain IT inventory list and licensing agreement information to ensure we remain in compliance. Contact appropriate maintenance, technical support, or programming personnel for hardware or software failures and escalate issues when needed. Install, upgrade, and maintain updates to software applications. Maintain daily tape backup and off-site tape storage. Maintain change control log for all computers. Represent the department and the organization favorably and in accordance with established Company standards and associate attributes at all times Other duties as assigned by management Level II – Fully meets the responsibilities of Level I plus the following: Installs, configures, and maintains personal computers and workstations. Serve as primary contact for administration activities and responsibilities for desktop computers, printers, phones, smartphones, software deployment, antivirus management, security and patches as well as additional technologies inclusive of both hardware and software. Maintain complete, timely and accurate record of administration. Organizes workload to ensure deadlines are met; schedules work assignments in order of priority and date received. Provides instruction and training to end users in operating systems, software applications, the telephone system, building security and manages card access. Set up computer, equipment, phone, email, voicemail, and security for new users, also make any changes or deletions for associate moves or terminations. Install, upgrade and maintain updates to software applications. Maintain change control log for all computers. Write and maintain knowledge-base articles and user documentation. Essential Knowledge, Skills and Abilities: Level I – Minimum High School Diploma or Equivalent required; Associate’s Degree preferred. A+ Certification, Network + Certification, Microsoft Certifications, ITIL or related training preferred but not required. Minimum of 1-3 years of experience general Help Desk/Desktop experience in an enterprise environment. Minimum of 1-3 years of experience with Windows desktop operating systems and Microsoft Office. Ability to identify and resolve computer system malfunctions and operational problems. Ability to perform complex tasks and to prioritize multiple projects. Practical knowledge of PC Operating Systems, printing to local and network printers, Exchange email, PC/Printer Hardware, and remote access. Working knowledge of OS image creation and deployment concepts and best practices. Working knowledge of laptop/desktop hardware. Experience with anti-virus and content filtering tools. Experience/basic understanding of Active Directory, networks and network cabling. Experience configuring mobile devices such as tablets and phones and WIFI connections. Strong attention to detail, the ability to multi-task and work in fast-paced environment. Experience working with service desk or help desk ticketing system(s). Displays willingness to make decisions; exhibits sound and accurate judgment; supports and explains reasoning for decisions; includes appropriate people in decision-making process; makes timely decisions. Aptitude to quickly learn and apply new systems, processes and applications with the ability to understand relationships and consequences. Ability to read & interpret documents i.e., internal SOPs, operating/maintenance instructions, and procedure manuals. Ability to evaluate new tools and technologies in terms of ease of use, security, and supportability. Goal-oriented, with excellent time management and organizational skills. Excellent interpersonal skills, with the ability to interact effectively and work efficiently with people at all levels in an organization. Ability to keep sensitive information confidential. Experience in lab or similar regulated or controlled environment. Level II - Fully meets the qualifications of Level I plus the following: Minimum of 3-7 years of experience general Desktop Technician /Help Desk experience in an enterprise environment. Minimum of 3-7 years of experience with Windows desktop operating systems. Minimum of 3-7 years of experience with Microsoft Office 365. Ability to develop migration plans and upgrade strategies. Ability to develop and manage to a project plan. Experience coordinating with 3rd party software/hardware vendors. Additional Information Personal Skills: Excellent analytical and problem-solving skills Excellent verbal/written communication skills. Fluent in English Scrum values: Commitment, Focus, Collaboration, Openness, Respect, Courage PREFERED CANDIDATES: The successful candidate will have a self-motivated, get-it-done attitude; the ability to think critically; enjoy working with teams spread globally and across cultures; a desire to learn in new areas; and the discipline to pay attention to deadlines, details and quality. Good communication and interpersonal skills to interact with team in Europe BE Computer Science/MCA or any other bachelor’s degree with the right experience Will be an added advantage if worked on Laboratory related applications PERFORMANCE APPRAISAL CRITERIA : Eurofins has a strong focus on Performance Management system. This includes quarterly calibrations, half-yearly reviews, and annual reviews. The KPIs shall be set and may vary slightly between projects. These will be clearly communicated, docum

Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - Research Scientist/ Sr, Research Scientist (L1/L2) Location: - Greater Noida Department: - DMPK Key Responsibilities ADME representative Understand the broader ADME requirements of various projects Ability to understand ADME-SAR and guide chemistry teams towards improving duggability of the NCEs Design DMPK strategy and implementation plan Conduct PK and PK/PD analysis through early pre-clinical development, and collaborate in PK/PD and efficacy study designs is a plus but not mandatory Interact with other cross functional teams (internal and external) and contribute to the progression of the compounds in the project Design tailor made ADME protocols for various projects Collate the obtained results and prepare presentations for internal and external meetings Contribute to the design of the critical path for various projects Addressing queries from the client. Lab management: Method development and analytical trouble shooting; Data generation, compilation, report preparation; Lab note book, record keeping; SOP writing Management towards optimising utilization of lab resources Keeping a track of FTE utilization in projects Keep track of CAPEX and OPEX requirements of the lab Prepare regular project updates and share with DMPK team management. Mentorship: Guide people/team on planning and execution of work and SOP writing Guide people/team towards developing required skill set to execute day to day activities in various projects Mentor juniors and train them on ongoing assays and technologies Should make sure that team follows ethical guidelines towards assay validation, data analysis, recording experiments, updating the data and maintenance. Publish results: Ability to communicate the scientific work to peer reviewed journals Fee-for-service (FFS) projects: Understand the requirements of various FFS clients and be able to design apt experiments Person Profile Qualification: - Ph D / MSc /M Tech Biochemistry, Pharmaceutical Chemistry, Biotech background. Experience: - 1 to 8 years (post PhD) / 10-12 yrs after M.Sc/ M.Tech Experience in a drug discovery industry/ CRO in DMPK department. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Jobsguru looking for a Medical Advisor for our pharma client in Mumbai. Contribute to the development of the medical components of the Brand Strategy and develop a Medical Plan. Mail CV search@jobsguru.in 9302574002 Shreya Jobsguru Consultant P Ltd Required Candidate profile Should be M. Pharma Excellent presentation and teaching skills Highly effective communicator both oral and written Can develop training material Excellent presentation and teaching skills

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. Scientific Business Analyst – Research Data and Analytics What You Will Do Let’s do this. Let’s change the world. In this vital role, you will primarily focus on analyzing scientific requirements from Global Research and translating them into efficient and effective information systems solutions. As a domain expert, the prospective BA collaborate with cross-functional teams to identify data product enhancement opportunities, perform data analysis, solve issues, and support system implementation and maintenance. Additionally, it will involve development of data product launch and user adoption strategy of Amgen Research Foundational Data Systems. Your expertise in business process analysis and technology will contribute to the successful delivery of IT solutions that drive operational efficiency and meet business objectives. Collaborate with geographically dispersed teams, including those in the US, EU and other international locations. Partner and ensure alignment of the Amgen India DTI site leadership and follow global standards and practices. Foster a culture of collaboration, innovation, and continuous improvement. Function as a Scientific Business Analyst, providing domain expertise for Research Data and Analytics within a Scaled Agile Framework (SAFe) product team Serve as Agile team scrum master or project manager as needed Serve as a liaison between global DTI functional areas and global research scientists, prioritizing their needs and expectations Create functional analytics dashboards and fit-for-purposes applications for quantitative research, scientific analysis and business intelligence (Databricks, Spotfire, Tableau, Dash, Streamlit, RShiny) Handle a suite of custom internal platforms, commercial off-the-shelf (COTS) software, and systems integrations Translate complex scientific and technological needs into clear, actionable requirements for development teams Develop and maintain release deliverables that clearly outlines the planned features and enhancements, timelines, and milestones Identify and handle risks associated with the systems, including technological risks, scientific validation, and user acceptance Develop documentations, communication plans and training plans for end users Ensure scientific data operations are scoped into building Research-wide Artificial Intelligence/Machine Learning capabilities Ensure operational excellence, cybersecurity and compliance. What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. This role requires expertise in biopharma scientific domains as well as informatics solution delivery. Additionally, extensive collaboration with global teams is required to ensure seamless integration and operational excellence. The ideal candidate will have a solid background in the end-to-end software development lifecycle and be a Scaled Agile practitioner, coupled with change management and transformation experience. This role demands the ability to deliver against key organizational strategic initiatives, develop a collaborative environment, and deliver high-quality results in a matrixed organizational structure. Basic Qualifications/Skills: Doctorate degree OR Master’s degree and 4 to 6 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR Bachelor’s degree and 6 to 8 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR Diploma and 10 to 12 years of Life Science/Biotechnology/Pharmacology/Information Systems experience Excellent problem-solving skills and a passion for solving complex challenges in drug discovery with technology and data Superb communication skills and experience creating impactful slide decks with data Collaborative spirit and effective communication skills to work seamlessly in a multi-functional team Familiarity with data analytics and scientific computing platforms such as Databricks, Dash, Streamlit, RShiny, Spotfire, Tableau and related programming languages like SQL, python, R Preferred Qualifications/Skills: BS, MS or PhD in Bioinformatics, Computational Biology, Computational Chemistry, Life Sciences, Computer Science or Engineering 3+ years of experience in implementing and supporting biopharma scientific research data analytics Demonstrated expertise in a scientific domain area and related technology needs Understanding of semantics and FAIR (Findability, Accessibility Interoperability and Reuse) data concepts Understanding of scientific data strategy, data governance, data infrastructure Experience with cloud (e.g. AWS) and on-premise compute infrastructure Familiarity with advanced analytics, AI/ML and scientific computing infrastructure, such as High Performance Compute (HPC) environments and clusters (e.g SLURM, Kubernetes) Experience with scientific and technical team collaborations, ensuring seamless coordination across teams and driving the successful delivery of technical projects Ability to deliver features meeting research user demands using Agile methodology An ongoing commitment to learning and staying at the forefront of AI/ML advancements. We understand that to successfully sustain and grow as a global enterprise and deliver for patients — we must ensure a diverse and inclusive work environment. Professional Certifications: SAFe for Teams certification (preferred) SAFe Scrum Master or similar (preferred) Soft Skills: Strong transformation and change management experience. Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. 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.

Roles and Responsibilities Provide clinical pharmacy services, including dispensing medications and counseling patients on their use. Manage inventory control by ordering supplies, maintaining stock levels, and ensuring accurate records. Assist with billing processes, ensuring timely submission of claims to insurance companies. Maintain confidentiality when handling sensitive patient information. Collaborate with healthcare teams to provide comprehensive care to customers. Desired Candidate Profile 1-6 years of experience as a retail pharmacist or related field. Bachelor's degree in Pharmacy (B.Pharma) from an accredited institution. Strong knowledge of pharmacology, pharmaceutics, and pharmacy practices. Excellent communication skills for effective customer service.

Roles and Responsibilities Provide clinical pharmacy services to patients, including dispensing medications and counseling on their use. Manage inventory levels of pharmaceuticals and supplies, ensuring accurate stock management. Conduct billing activities accurately and efficiently for patient treatments. Maintain confidentiality when handling sensitive patient information. Collaborate with healthcare teams to provide comprehensive care to patients. Desired Candidate Profile 1-6 years of experience as a Retail Pharmacist or equivalent role. Bachelor's degree in Pharmacy (B.Pharma) from an accredited institution. Strong knowledge of clinical pharmacy practices, pharmacology, medicine, and pharmaceutics. Excellent communication skills for effective patient interaction.

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast-track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations to be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work Job Description: • Act as SME for safety business and track industry trends relevant to safety • Work in collaboration with the Sales and the Solutioning teams to improve win ratio and opportunity conversions • Responsible for improving capability presentations and Identifying service areas and solutions and work with the operational leadership to build capabilities • Participates in the analysis and definition of efficient, cost effective and creative solutions deliver competitive value propositions to the industry • Build partnership with senior leadership across the industry in Safety and PV • Represent the company in trade conferences, speaker sessions etc. • Identify and build potentially synergistic partnerships to expand client and service footprints • Be part of safety consulting engagements as well as provide oversight and expertise on operations as needed - MBBS/ MD with a minimum of 14-18years of experience in drug safety or a related field; Master/Diploma in Management degree is added advantage - Experience in the pharmaceutical industry, preferably in drug safety, pharmacovigilance, or clinical development - Knowledge of pharmacology, toxicology, and clinical trial methodology - Understanding of FDA and international regulatory requirements related to drug safety and pharmacovigilance - Strong analytical and problem-solving skills - Excellent communication and interpersonal skills, with the ability to work effectively in cross-functional teams - Demonstrated ability to prioritize tasks and manage multiple projects simultaneously - Proficiency in data analysis tools (e.g., Excel, SAS) and safety databases (e.g., Argus, ARISg) - Good communication skils and relationship building skills - Act as SME for safety business and track industry trends relevant to safety - Work in collaboration with the Sales and the Solutioning teams to improve win ratio and opportunity conversions - Responsible for improving capability presentations and Identifying service areas and solutions and work with the operational leadership to build capabilities - Participates in the analysis and definition of efficient, cost effective and creative solutions deliver competitive value propositions to the industry - Build partnership with senior leadership across the industry in Safety and PV - Represent the company in trade conferences, speaker sessions etc. - Identify and build potentially synergistic partnerships to expand client and service footprints - Be part of safety consulting engagements as well as provide oversight and expertise on operations as needed Show more Show less

Job Description Responsibility New Product Development/ Existing product enhancement : Generate new product ideas Build People: Provide on job feedback and coaching Build Culture: Act as first point of contact for communication, interpretation, and implementation of management decisions Primary Responsibility Research Management: Project management (planning and tracking for efficient delivery), quality management (ensuring adherence to research process and protocols), and report execution BD Initiatives – development of proposal and executing assigned BD initiatives (Newsletters, Whitepapers etc.) Knowledge Management: transfer knowledge/project learnings to the functional group/organization Secondary Responsibility New Product Development/ Existing product enhancement : Generate new product ideas Build People: Provide on job feedback and coaching Build Culture: Act as first point of contact for communication, interpretation, and implementation of management decisions Skills and Expertise Technically strong with orientation for commercial considerations or vice-versa – should possess strong logical and analytical acumen Independent handling and efficient delivery of the project(s) including engagement with internal and external stakeholders Drive thought leadership and BD engagement initiatives (including development of proposals) for the assigned TA/Functional Area Take lead in resource development through trainings (including on the job training) and development/up-dation of framework or protocols for strategic analysis Experience 7-10 years of experience in similar/allied role in Advisory organization or Pharmaceutical Industry Educational Qualifications Graduate/Post- graduate with a management degree from a reputed institute Pharm/M. Pharm, MBA/MBBS /MD or PhD (Immunology, Oncology, Molecular Biology, Biochemistry, Pharmacology and Life Sciences), preferably from a premier institute Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others. Show more Show less

We are seeking an experienced and passionate Nursing Tutor to join our coaching institute, specializing in preparing students for competitive nursing exams such as NORCET, PGIMER, MNS, AIIMS, and other nursing officer exams . The ideal candidate will have a deep understanding of nursing concepts, excellent teaching skills, and a strong commitment to helping students succeed in their exams and build their careers in nursing. Key Responsibilities : Exam-Focused Teaching : Deliver high-quality lectures and tutorial sessions focused on competitive exams for nursing officer positions. Ensure that the content is aligned with the syllabus of NORCET, PGIMER, MNS, AIIMS, and other related exams. Subject Expertise : Teach core nursing subjects including Anatomy, Physiology, Nursing Foundation, Medical-Surgical Nursing, Pharmacology, and other relevant topics based on exam requirements. Question Practice and Exam Preparation : Help students prepare for exams by conducting mock tests, quizzes, and solving previous years' question papers. Provide strategies for effective time management and exam techniques. Student Mentorship : Provide individual attention and academic support to students, addressing their doubts, helping with study plans, and offering motivation throughout their preparation journey. Study Materials and Resources : Create and provide comprehensive study materials, notes, and resources tailored to the competitive exam syllabus. Keep materials up to date with the latest exam trends and guidelines. Assessments and Feedback : Conduct regular assessments and provide constructive feedback to students. Track student progress and help them improve in areas where they face difficulties. Group Discussions and Doubt Clearing : Organize group discussions, doubt-solving sessions, and interactive classes to enhance students' understanding and application of key nursing concepts. Monitoring Progress : Keep track of student performance and progress, adjusting teaching methods as necessary to ensure students stay on track to achieve their goals. Exam Strategies : Provide students with tips on tackling competitive exams, including answering techniques, time management, and stress reduction methods. Skills & Qualifications : Educational Qualifications : Registered Nurse (RN) with a Bachelor’s degree in Nursing (BSc Nursing) or a Master’s degree in Nursing (MSc Nursing). Experience : Proven experience in teaching or tutoring nursing students, preferably in preparing for competitive exams like NORCET, PGIMER, MNS, or AIIMS. Subject Knowledge : Strong knowledge of nursing subjects and concepts required for competitive exams. Teaching Skills : Excellent communication, presentation, and interpersonal skills. Ability to explain complex nursing topics in a simple and understandable way. Exam Expertise : Familiarity with the structure, pattern, and syllabus of major nursing competitive exams. Passion for Education : A genuine interest in helping students succeed and building their confidence to excel in competitive exams. Problem-Solving : Ability to identify students' weaknesses and provide tailored solutions to improve their understanding and performance. Technological Proficiency : Familiarity with online teaching tools and platforms is an advantage, especially for students attending remote classes. Preferred Qualifications : Prior experience in coaching students for competitive exams in nursing. Certification in Nursing Education or additional relevant qualifications. Strong motivational skills to inspire students to achieve their best. Ability to design and develop exam-oriented study materials. Benefits : Competitive salary and performance-based incentives. Flexible working hours (for part-time roles). Access to ongoing training and professional development. A supportive and collaborative teaching environment. Opportunity to make a meaningful impact on students' careers in nursing. Job stability and opportunities for advancement in a growing coaching institute. Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Schedule: Day shift Work Location: In person

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. Scientific Business Analyst – Research Data and Analytics What you will do Let’s do this. Let’s change the world. In this vital role, you will primarily focus on analyzing scientific requirements from Global Research and translating them into efficient and effective information systems solutions. As a domain expert, the prospective BA collaborate with cross-functional teams to identify data product enhancement opportunities, perform data analysis, solve issues, and support system implementation and maintenance. Additionally, it will involve development of data product launch and user adoption strategy of Amgen Research Foundational Data Systems. Your expertise in business process analysis and technology will contribute to the successful delivery of IT solutions that drive operational efficiency and meet business objectives. Collaborate with geographically dispersed teams, including those in the US, EU and other international locations. Partner and ensure alignment of the Amgen India DTI site leadership and follow global standards and practices. Foster a culture of collaboration, innovation, and continuous improvement. Function as a Scientific Business Analyst, providing domain expertise for Research Data and Analytics within a Scaled Agile Framework (SAFe) product team Serve as Agile team scrum master or project manager as needed Serve as a liaison between global DTI functional areas and global research scientists, prioritizing their needs and expectations Create functional analytics dashboards and fit-for-purposes applications for quantitative research, scientific analysis and business intelligence (Databricks, Spotfire, Tableau, Dash, Streamlit, RShiny) Handle a suite of custom internal platforms, commercial off-the-shelf (COTS) software, and systems integrations Translate complex scientific and technological needs into clear, actionable requirements for development teams Develop and maintain release deliverables that clearly outlines the planned features and enhancements, timelines, and milestones Identify and handle risks associated with the systems, including technological risks, scientific validation, and user acceptance Develop documentations, communication plans and training plans for end users Ensure scientific data operations are scoped into building Research-wide Artificial Intelligence/Machine Learning capabilities Ensure operational excellence, cybersecurity and compliance. What we expect of you We are all different, yet we all use our unique contributions to serve patients. This role requires expertise in biopharma scientific domains as well as informatics solution delivery. Additionally, extensive collaboration with global teams is required to ensure seamless integration and operational excellence. The ideal candidate will have a solid background in the end-to-end software development lifecycle and be a Scaled Agile practitioner, coupled with change management and transformation experience. This role demands the ability to deliver against key organizational strategic initiatives, develop a collaborative environment, and deliver high-quality results in a matrixed organizational structure. Basic Qualifications/Skills: Doctorate degree OR Master’s degree and 4 to 6 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR Bachelor’s degree and 6 to 8 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR Diploma and 10 to 12 years of Life Science/Biotechnology/Pharmacology/Information Systems experience Excellent problem-solving skills and a passion for solving complex challenges in drug discovery with technology and data Superb communication skills and experience creating impactful slide decks with data Collaborative spirit and effective communication skills to work seamlessly in a multi-functional team Familiarity with data analytics and scientific computing platforms such as Databricks, Dash, Streamlit, RShiny, Spotfire, Tableau and related programming languages like SQL, python, R Preferred Qualifications/Skills: BS, MS or PhD in Bioinformatics, Computational Biology, Computational Chemistry, Life Sciences, Computer Science or Engineering 3+ years of experience in implementing and supporting biopharma scientific research data analytics Demonstrated expertise in a scientific domain area and related technology needs Understanding of semantics and FAIR (Findability, Accessibility Interoperability and Reuse) data concepts Understanding of scientific data strategy, data governance, data infrastructure Experience with cloud (e.g. AWS) and on-premise compute infrastructure Familiarity with advanced analytics, AI/ML and scientific computing infrastructure, such as High Performance Compute (HPC) environments and clusters (e.g SLURM, Kubernetes) Experience with scientific and technical team collaborations, ensuring seamless coordination across teams and driving the successful delivery of technical projects Ability to deliver features meeting research user demands using Agile methodology An ongoing commitment to learning and staying at the forefront of AI/ML advancements. We understand that to successfully sustain and grow as a global enterprise and deliver for patients — we must ensure a diverse and inclusive work environment. Professional Certifications: SAFe for Teams certification (preferred) SAFe Scrum Master or similar (preferred) Soft Skills: Strong transformation and change management experience. Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. 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.

This role is for one of our clients Industry: Hospitals and Health Care Seniority level: Associate level Min Experience: 0 years JobType: full-time About The Opportunity We are seeking a dedicated and detail-oriented Consultant Anesthesiologist to join a leading multi-specialty hospital in Bhavnagar. This opportunity is ideal for early-career medical professionals looking to build a long-term career in a technologically advanced, patient-centric clinical environment. You will play a vital role in delivering safe, effective anesthesia care across a broad range of surgical specialties, working alongside some of the region’s most skilled medical teams. If you are committed to clinical excellence, collaborative teamwork, and continuous learning, this role offers the ideal platform to grow and make a meaningful impact. Key Responsibilities Anesthesia Delivery & Patient Monitoring Administer general, regional, and local anesthesia for surgical, diagnostic, and therapeutic procedures. Continuously monitor patient vitals and anesthetic depth to ensure intraoperative safety and stability. Tailor anesthesia techniques to suit individual patient conditions, comorbidities, and procedural requirements. Preoperative & Postoperative Patient Management Conduct thorough pre-anesthetic evaluations including risk assessment and patient counseling. Manage postoperative recovery, pain control protocols, and potential anesthesia-related complications. Maintain clear communication with patients and families about anesthesia procedures and expectations. Interdisciplinary Collaboration Work closely with surgeons, intensivists, physicians, and nursing staff to provide seamless perioperative care. Participate in pre-surgical briefings, case reviews, and critical care planning for high-risk patients. Documentation & Compliance Maintain accurate and comprehensive medical records of all anesthesia interventions and observations. Ensure adherence to institutional policies, safety standards, and national medical guidelines. Mentorship & Clinical Learning Supervise and support residents, fellows, and medical interns during procedures. Demonstrate the correct use of monitoring and anesthesia equipment, emphasizing patient safety and efficiency. Professional Growth & Contribution Engage in hospital-led clinical audits, quality assurance activities, and department meetings. Stay abreast of the latest research, protocols, and technologies in anesthesiology through CME programs and medical conferences. Candidate Profile Qualifications: MD / DNB in Anesthesiology from a recognized medical institution. Must hold valid registration with MCI or relevant State Medical Council. Experience: 0–3 years of post-qualification experience (Freshers encouraged to apply). Core Competencies: Strong foundation in pharmacology, physiology, and anesthesia techniques. Confidence in handling emergencies and making critical intraoperative decisions. Clear and empathetic communication skills with both patients and medical teams. Strong commitment to patient care, ethical practice, and continuous improvement. Why Join Us? Be part of a highly reputed multi-specialty hospital with advanced infrastructure. Learn and grow under the mentorship of seasoned medical professionals. Enjoy a collaborative work environment that values compassion, innovation, and clinical integrity. Competitive compensation package with opportunities for academic contribution and skill enhancement.

Job Description Responsibility New Product Development/ Existing product enhancement : Generate new product ideas Build People: Provide on job feedback and coaching Build Culture: Act as first point of contact for communication, interpretation, and implementation of management decisions Primary Responsibility Research Management: Project management (planning and tracking for efficient delivery), quality management (ensuring adherence to research process and protocols), and report execution BD Initiatives – development of proposal and executing assigned BD initiatives (Newsletters, Whitepapers etc.) Knowledge Management: transfer knowledge/project learnings to the functional group/organization Secondary Responsibility New Product Development/ Existing product enhancement : Generate new product ideas Build People: Provide on job feedback and coaching Build Culture: Act as first point of contact for communication, interpretation, and implementation of management decisions Skills and Expertise Technically strong with orientation for commercial considerations or vice-versa – should possess strong logical and analytical acumen Independent handling and efficient delivery of the project(s) including engagement with internal and external stakeholders Drive thought leadership and BD engagement initiatives (including development of proposals) for the assigned TA/Functional Area Take lead in resource development through trainings (including on the job training) and development/up-dation of framework or protocols for strategic analysis Experience 7-10 years of experience in similar/allied role in Advisory organization or Pharmaceutical Industry Educational Qualifications Graduate/Post- graduate with a management degree from a reputed institute Pharm/M. Pharm, MBA/MBBS /MD or PhD (Immunology, Oncology, Molecular Biology, Biochemistry, Pharmacology and Life Sciences), preferably from a premier institute Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.

Job description Responsibility New Product Development/ Existing product enhancement : Generate new product ideas Build People: Provide on job feedback and coaching Build Culture: Act as first point of contact for communication, interpretation, and implementation of management decisions Primary Responsibility Research Management: Project management (planning and tracking for efficient delivery), quality management (ensuring adherence to research process and protocols), and report execution BD Initiatives – development of proposal and executing assigned BD initiatives (Newsletters, Whitepapers etc.) Knowledge Management: transfer knowledge/project learnings to the functional group/organization Secondary Responsibility New Product Development/ Existing product enhancement : Generate new product ideas Build People: Provide on job feedback and coaching Build Culture: Act as first point of contact for communication, interpretation, and implementation of management decisions Skills and Expertise Technically strong with orientation for commercial considerations or vice-versa – should possess strong logical and analytical acumen Independent handling and efficient delivery of the project(s) including engagement with internal and external stakeholders Drive thought leadership and BD engagement initiatives (including development of proposals) for the assigned TA/Functional Area Take lead in resource development through trainings (including on the job training) and development/up-dation of framework or protocols for strategic analysis Experience 7-10 years of experience in similar/allied role in Advisory organization or Pharmaceutical Industry Educational Qualifications Graduate/Post- graduate with a management degree from a reputed institute Pharm/M. Pharm, MBA/MBBS /MD or PhD (Immunology, Oncology, Molecular Biology, Biochemistry, Pharmacology and Life Sciences), preferably from a premier institute Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.