Pharma, Clinical Research & Healthcare Jobs in India
511 open roles from pharma companies, CROs and hospitals, with new openings added most days. Apply directly through each employer's own page or contact.
Showing 101–125 of 170 jobs
Scientist – Research Computational Biology
Amgen
Hyderabad5+ Years · Onsite25 SeptAmgen's ARIA Computational Biology team in Hyderabad sits at the intersection of large-scale data science and disease biology, and this Scientist role is central to how the company replenishes its therapeutic pipeline. Rather than supporting discovery from the periphery, the position directly shapes which targets advance into Amgen's oncology, inflammation and immunology portfolios. The scientist mines multi-modal omics and screening data to characterise disease endotypes, test therapeutic hypotheses and surface novel targets, while building reusable platforms that make those insights scalable across therapeutic modalities. For an experienced computational biologist, this is a rare chance to work on foundational target biology with a global biotech leader, applying long-read transcriptomics, single-cell atlases and transcriptional foundation models inside a genuinely cross-functional research environment with strong scientific visibility.
Ophthalmology Squad Lead
Roche
Kolkata5+ Years · Onsite25 SeptRoche’s Ophthalmology Squad Lead role in Kolkata is a senior commercial and strategic leadership position within one of the company’s most important therapy areas in India. The incumbent owns the Outcome Based Plan, translating disease-area strategy into measurable patient impact, partnerships and account penetration. This is a high-visibility opportunity to shape the ophthalmology ecosystem, lead cross-functional squads and co-create value propositions with key corporate and regional accounts. The position matters because Roche’s ophthalmology portfolio is central to future growth, requiring visionary leadership, execution excellence and uncompromising compliance. For an experienced pharma leader, it offers the chance to influence access, innovation adoption and team development while working with global and Indian stakeholders to improve retinal and eye-care outcomes.
Electrical Engineering Technician – Pharmaceutical Manufacturing
Gsk
Nashik5+ Years · Onsite25 SeptGSK’s Nashik manufacturing site is a critical node in the company’s global supply chain, producing medicines and vaccines that reach patients worldwide. This Electrical Engineering Technician role is central to maintaining uninterrupted power and utility services across high-voltage and low-voltage systems, HVAC, boilers, chillers, and compressed air. By executing preventive, predictive, and breakdown maintenance, the technician directly protects product quality, regulatory compliance, and commercial output. The position offers a compelling career opportunity for hands-on electrical professionals who want to deepen their expertise in pharmaceutical manufacturing, automation, and GxP environments. Working cross-functionally with production, quality, and EHS teams, you will help GSK deliver on its ambition to impact 2.5 billion people by 2030 while building a resilient, future-ready engineering career.
Senior Statistical Programmer
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi's Business Operations hub in Hyderabad anchors a global network of centralized statistical, medical and commercial capabilities serving Specialty Care, Vaccines, General Medicines, Consumer Healthcare and R&D. Within that structure, the Senior Statistical Programmer is a linchpin of Medical Affairs biostatistics — converting raw clinical trial and registry data into rigorous, QC'd tables, figures and listings that underpin abstracts, posters, manuscripts and regulatory-grade evidence. The position sits at the intersection of statistical science and programming craft, giving the holder direct exposure to Sanofi's global portfolio and to senior biostatisticians across geographies. For experienced SAS programmers who want their code to shape how medicines are described to physicians, regulators and payers worldwide, this is a rare chance to combine deep technical work with visible scientific impact.
Associate Manager - Manufacturing Quality Assurance (Upstream)
Pfizer
Visakhapatnam5+ Years · Onsite25 SeptThis Associate Manager - MQA Upstream role at Pfizer’s Vizag sterile manufacturing site is a critical quality leadership position supporting cGMP compliance across solution/emulsion preparation, vial and ampoule washing, depyrogenation, filling, capping, and collection. The position safeguards patient safety and product quality for Pfizer’s sterile injectable portfolio, where regulatory scrutiny from USFDA, MHRA, and TGA is intense. By reviewing electronic batch records, assessing AMPS exceptions, overseeing alarm and trend reports, and investigating deviations, the MQA professional ensures every batch meets Pfizer standards and global regulatory expectations. This is a compelling opportunity for experienced QA professionals to deepen expertise in sterile manufacturing, electronic batch systems, and inspection readiness while influencing shop-floor quality culture, process simplification, and continuous improvement at one of Pfizer’s key India sites.
Associate Manager – Manufacturing Quality Assurance
Pfizer
Visakhapatnam5+ Years · Onsite25 SeptPfizer’s Associate Manager, Manufacturing Quality Assurance, based in Visakhapatnam, is a critical cGMP compliance role supporting terminal sterilization, visual inspection and packaging operations. The position ensures that manufacturing processes, batch records and equipment systems remain inspection-ready for global regulators such as USFDA, MHRA and TGA. This is not a generic QA job: it directly protects patient safety, product quality and Pfizer’s commercial supply continuity. The role offers a strong platform for experienced pharma QA professionals to deepen expertise in sterile operations, electronic batch record review, deviation/AMP impact assessment and audit management. With Pfizer’s science- and risk-based quality culture, the successful candidate gains exposure to advanced manufacturing systems, cross-functional troubleshooting and process simplification, making it an excellent long-term career move within global pharmaceutical operations.
Medical Advisor Head Office - Mumbai
Boehringer Ingelheim
Mumbai5+ Years · Onsite25 SeptMedical Affairs role focused on scientific engagement, therapeutic-area insights, medical projects, KOL development, medico-marketing strategy, product registration support and medical labeling activities.
Manager QA - EPD Quality Systems
Abbott
Mumbai5+ Years · Onsite25 SeptManager QA – EPD Quality Systems responsible for managing Quality Systems related initiatives within the EPD Quality System organization to ensure safe, effective and quality products.
Area Manager
Lupin
Ahmedabad5+ Years · Onsite25 SeptManage regional sales operations, drive primary and secondary sales targets, and lead a team of medical representatives in Ahmedabad.
Scientist, Biomarker Analysis
Amgen
Hyderabad5+ Years · Onsite25 SeptAmgen's Scientist, Biomarker Analysis role in Hyderabad is a strategic addition to the Global Development - Precision Medicine organization, specifically within Computational Biology and Translational Analytics. As Amgen expands its India innovation footprint, this position will deliver high-quality clinical biomarker analytics across oncology, inflammation, rare disease, cardiovascular/metabolic, and obesity programs. The scientist will transform complex multi-omics, imaging, and clinical trial data into actionable translational insights that inform target engagement, patient stratification, mechanism validation, and benefit-risk decisions. This is a compelling opportunity for a quantitative biologist to work at the interface of drug development, advanced statistics, and responsible AI, influencing global portfolio decisions while helping build a high-impact precision medicine capability at Amgen India. The role offers deep scientific ownership, cross-functional collaboration, and exposure to late-stage clinical programs.
Associate Marketing Director – Diabetes Care
Abbott
Mumbai5+ Years · Onsite25 SeptAbbott's Associate Marketing Director for ADC India sits on the India Leadership Team and owns the strategic marketing agenda for Abbott Diabetes Care — the business behind FreeStyle Libre, the world's leading continuous glucose monitoring (CGM) franchise. This is a high-visibility commercial leadership role in which marketing directly shapes diabetes outcomes at national scale: brand strategy, HCP and consumer engagement, digital and CRM journeys, and customer experience all fall within this mandate. Because India is one of the fastest-growing diabetes markets globally, with more than 100 million people living with the condition, the position carries outsized strategic weight in Abbott's global CGM expansion story. For a seasoned pharma, medical device or consumer health marketer, it offers a rare blend of P&L-adjacent impact, cross-functional leadership across Sales, Medical and Commercial, and exposure to area and global marketing forums that can accelerate a path to Marketing Director or General Manager roles.
Associate Manager, Externally Sponsored Research
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi Business Operations (SBO) in Hyderabad seeks an Associate Manager, Externally Sponsored Research (ESR) to oversee investigator-sponsored studies and externally sponsored collaborations from concept submission through closeout. This role sits at the intersection of clinical research, medical governance, and operational excellence, ensuring that unsolicited research support requests are routed for scientific review and managed in compliance with Sanofi SOPs, ICH-GCP, and local regulations. It is critical to Sanofi's Specialty Care, Vaccines, General Medicines, and R&D pipelines because ESRs generate real-world evidence and expand research partnerships. The position offers deep exposure to global stakeholders, SRC coordination, study start-up, product supply, contracting, and audit readiness. For professionals with clinical trial project management experience, it is a compelling opportunity to build specialized expertise in externally sponsored research operations while contributing to compliant, timely delivery of studies that inform medical and commercial strategy.
R&D Global Regulatory Affairs CMC Lead
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi’s Global Regulatory Affairs CMC & Device Organization seeks an R&D GRA CMC Lead in Hyderabad to shape regulatory strategies for pharmaceuticals, biologics, vaccines, and combination products. This senior role is central to Sanofi’s pipeline, bridging R&D, manufacturing, and health authorities such as the US FDA and EMA. The CMC Lead ensures dossiers meet global quality and compliance standards, accelerates approvals, and mitigates regulatory risks across the product lifecycle. As a strategic partner, the position influences cross-functional teams, regulatory policy, and digital innovation, including AI-enabled regulatory workflows. For experienced CMC professionals, this is a high-visibility opportunity to lead complex submissions, negotiate with regulators, and advance patient access to innovative therapies while growing within a world-class regulatory network.
Assistant Manager – Pharmacovigilance Local Case Intake (Japanese Language)
AstraZeneca
Bengaluru5+ Years · Onsite25 SeptAstraZeneca's Local Case Intake function is the front door of the company's patient-safety ecosystem, and this Assistant Manager role owns it for the Japanese market. Leading a team of Local Case Intake Advisors, you will make sure every adverse event report originating from Japanese Marketing Companies is captured, triaged, followed up and submitted within regulatory clocks. Because Japan is one of AstraZeneca's largest and most tightly regulated commercial markets, accuracy here directly protects licence continuity, Health Authority credibility and patient trust. This is a compelling next step for a pharmacovigilance professional with Japanese language capability who wants to move from individual case processing into people leadership, gaining structured exposure to PMDA interactions, Pharmacovigilance System Master File governance, inspection readiness and global safety transformation work inside a digitally enabled organisation.
Associate Manager - MSAT (Commissioning & Qualification)
Pfizer
Vizag5+ Years · Onsite25 SeptPfizer’s Manufacturing Science & Technology (MSAT) group at Vizag plays a critical role in commissioning, qualification and validation of sterile injectable manufacturing assets. The Associate Manager – MSAT (C&Q) ensures equipment, utilities, facilities and processes are qualified to cGMP, FDA and Pfizer Quality Standards, directly protecting product sterility, patient safety and regulatory compliance. This position matters because Vizag supports regulated-market injectables, where robust validation underpins every batch release. The role offers exposure to complex sterile processes, cleaning validation, computer system validation, audits and technology transfers. For pharma professionals with QA, validation or sterile manufacturing experience, it is a compelling opportunity to deepen technical expertise, work cross-functionally and influence compliance strategy at a global scale while building a pathway toward senior quality and MSAT leadership.
Regulatory Affairs CMC Team Lead
Sanofi
Hyderabad5+ Years · Onsite25 SeptThis R&D GRA CMC Team Lead role at Sanofi in Hyderabad is a senior regulatory affairs leadership position within the Global Regulatory Affairs CMC & Device Organization. The incumbent will shape global Chemistry, Manufacturing, and Controls strategies for pharmaceuticals, biologics, vaccines, and combination products, directly influencing approval timelines and lifecycle management. As a critical bridge between technical development, manufacturing, and health authorities, this role ensures Sanofi's innovative therapies reach patients with speed and compliance. The position offers exceptional exposure to FDA, EMA, and other global regulators, matrixed project teams, and cutting-edge digital regulatory tools such as Veeva Vault. For regulatory professionals seeking to lead strategy, mentor specialists, and drive organizational change in a world-class biopharma environment, this is a compelling career step with significant influence on Sanofi's commercial and clinical pipeline.
Manager QA – EPD Quality Systems
Abbott
Mumbai5+ Years · Onsite24 SeptManage Quality Systems initiatives within Abbott's EPD Quality System organization, supporting Quality Management System processes with emphasis on Third-Party Manufacturer and Supplier Quality Management. The role drives continuous improvement, regulatory compliance, global initiatives, and quality-system governance.
Senior Medical Advisor
Pfizer
Mumbai5+ Years · Onsite24 SeptProvide scientific and medical expertise to support medical strategy, launch readiness, evidence generation, and external engagement for Specialty Care and Internal Medicine pipeline products while ensuring scientific integrity and regulatory compliance.
Associate Consultant Neuro Surgery
Fortis Healthcare
Bangalore5+ Years · Onsite24 SeptSeeking an Associate Consultant Neuro Surgery to deliver expert surgical care, manage neurological disorders, and contribute to clinical excellence at People Tree Hospital.
Consultant – Anesthesiologist
AIMS India
Faridabad5+ Years · Onsite24 SeptSeeking an experienced Consultant Anesthesiologist to provide expert anesthetic care, manage critical care units, and ensure patient safety during surgical procedures.
Director, Process Development- Drug Product
Amgen
Hyderabad5+ Years · Onsite24 SeptLead and build the Drug Product Technologies organization at Amgen Hyderabad, driving process development, digital transformation, and global biotech deliverables.
Medical Governance Lead
Novartis
India5+ Years · Onsite24 SeptMedical Governance Lead accountable for strengthening governance, compliance, SOP adherence, MLR oversight, audit readiness and Managed Access Program governance across Medical Affairs activities in India.
Attending Consultant Radiology
Fortis Escorts Heart Institute & Research Centre
Delhi NCR5+ Years · Onsite23 SeptProvide expert radiological diagnostic and consultative services at Fortis Escorts Heart Institute in Delhi.
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Speciality Care Advisor - Cardiology (field based in Mumbai)
Bristol Myers Squibb
Mumbai5+ Years · Onsite23 SeptDrive territory performance for Cardiology by identifying and mapping healthcare accounts, engaging healthcare professionals, supporting scientific activities and executing commercial strategies in line with BMS objectives and values.
Director, Process Development - Drug Product
Amgen
Hyderabad5+ Years · Onsite23 SeptLead the establishment and growth of Amgen's Drug Product Technologies organization in Hyderabad, building a high-performing team and operating model while expanding global drug product process-development capabilities through technical, digital and cross-functional innovation.