Pharma, Clinical Research & Healthcare Jobs in India
518 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 1–25 of 78 jobs
Analyst Customer Facing Effectiveness
Sanofi
Hyderabad2-5 Years · OnsiteYesterdaySanofi is hiring an Analyst Customer Facing Effectiveness in Hyderabad to support commercial operations through incentive plan analysis, sales target allocation, and sales force effectiveness tracking. The role sits within the global Go-to-Market Capabilities team and requires analytical skills and commercial operations experience.
Statistical Programmer
Sanofi
Hyderabad2-5 Years · Onsite4 days agoSanofi is hiring a Statistical Programmer in Hyderabad to support Medical Affairs biostatistics within Sanofi Business Operations. The role centres on building QC'd statistical outputs — tables, figures and listings — for publications and ad-hoc analyses, using SAS and CDISC standards.
Central Clinical Research Associate
Sanofi
Hyderabad2-5 Years · Onsite6 days agoSanofi is hiring a Central Clinical Research Associate in Hyderabad to support rare disease registry studies. The role coordinates with principal investigators and site staff and covers start-up, monitoring, data review and site-management tasks under ICH-GCP.
R&D Scientific Competitive Intelligence Analyst
Sanofi
Hyderabad2-5 Years · Onsite20 days agoSanofi is recruiting an R&D Scientific Competitive Intelligence Analyst for its Hyderabad offshore hub, where patent data is used to map competitor innovation and shape R&D portfolio choices. The position sits in the Competitive Intelligence group of the Global R&D Strategy and Portfolio Management team.
Quality Assurance Specialist
Sanofi
Verna2-5 Years · Onsite7 OctSanofi is hiring a Quality Assurance Specialist for its Goa site in Verna Industrial Estate. The position suits professionals with 2 to 5 years of experience in IPQA, batch record review, and shopfloor quality governance, with B.Pharm or M.Pharm qualification. The role involves three-shift working.
Associate, Membership – Contracts & Pricing Execution
Amgen
Hyderabad2-5 Years · Onsite7 OctAmgen is hiring an Associate, Membership – Contracts & Pricing Execution in Hyderabad. The role supports U.S. pharmaceutical membership operations covering customer eligibility, contract alignment, pricing-related processes, customer setup, data maintenance, and compliance activities.
HR Specialist
Syneos Health
Delhi NCR2-5 Years · Onsite6 OctSyneos Health is hiring an HR Specialist in Gurgaon to provide operational support across employee lifecycle processes, HR records, employee queries, compliance activities, and HR service delivery. The role requires a bachelor's degree and 3 years of HR operations experience, along with hands-on Workday HCM and HR ticketing tool experience.
Regulatory Affairs Associate II
Teva Pharmaceuticals
Mumbai2-5 Years · Onsite6 OctTeva Pharmaceuticals is hiring a Regulatory Affairs Associate II in Navi Mumbai for work involving FDA submissions, post-approval changes, annual reports and regulatory documentation. The role is intended for candidates with at least four years of pharmaceutical industry experience and relevant regulatory, analytical, quality, laboratory or production exposure.
Manager – Standards Medical Writer (Biomedical Data Stewardship)
Amgen
Hyderabad2-5 Years · Onsite5 OctAmgen is expanding its global Biomedical Data Stewardship (BMDS) capabilities in India, and this Manager, Standards Medical Writer role sits at the intersection of medical writing, clinical data standards, and regulatory governance. Based in Hyderabad, the position supports Amgen's Center for Design & Analysis by advancing protocol standards, structured authoring, and metadata repository (MDR) execution. The role is critical to ensuring protocols are fit-for-purpose, inspection-ready, and aligned with global clinical development strategy across therapeutic areas. By partnering with Global Regulatory Writing, Clinical Development, Regulatory, and TA SMEs, the writer-manager helps harmonize protocol language, govern libraries, and improve data quality from authoring through submission. This is a compelling opportunity for life-sciences professionals seeking global cross-functional exposure, influence over enterprise standards, and a career path in medical writing, clinical data governance, or regulatory operations within a top-tier biopharma.
Filling Instrumentation Engineer
Pfizer
Visakhapatnam2-5 Years · Onsite4 OctPfizer's Vizag facility is a cornerstone of its global sterile injectables and vaccine manufacturing network. The Filling Instrumentation Engineer role is central to maintaining uninterrupted, compliant operation of critical fill-finish equipment, including vial washing, tunnel sterilization, filling, capping, and inspection lines. By ensuring precise calibration, predictive maintenance, and rapid troubleshooting of instrumentation and automation systems, this engineer directly supports the delivery of life-saving medicines to patients worldwide. The position offers a unique opportunity to work with advanced Siemens, Allen-Bradley, or DeltaV platforms in a GMP-regulated environment. As part of a forward-thinking engineering team, you will contribute to capacity expansions, automation upgrades, and continuous improvement projects, accelerating your career in pharmaceutical engineering while making a tangible impact on global health.
Officer / Senior Officer – Quality Assurance (OSD)
Sun Pharmaceutical Industries Ltd
Halol2-5 Years · Onsite2 OctQuality Assurance opportunity at Sun Pharma's Halol plant focused on in-process quality assurance, batch documentation, validation, manufacturing oversight and cGMP compliance for oral solid dosage (OSD) operations.
Scientific Writer - Health Economics and Value Assessment (HEVA)
Sanofi
Hyderabad2-5 Years · Onsite1 OctSanofi’s Global Hub in Hyderabad is a strategic engine for medical, HEVA, and commercial excellence. As a Scientific Writer – Health Economics and Value Assessment (HEVA), you will translate complex health economic and value evidence into clear, compliant publications and communication tools. This role is pivotal for demonstrating product value to payers, healthcare professionals, and internal stakeholders, directly supporting access and reimbursement decisions across Specialty Care, Vaccines, General Medicines, and CHC. You will partner with global HEVA, RWE, and scientific communication teams, managing deliverables from manuscripts and abstracts to Core Value Decks. This is an outstanding opportunity to build therapeutic area expertise, influence global value narratives, and grow within a world-class pharmaceutical organization committed to innovation and patient impact.
Scientific Writer HEVA
Sanofi
Hyderabad2-5 Years · Onsite1 OctScientific Writer – Health Economics and Value Assessment (HEVA) develops high-quality HEVA communications and evidence-based content supporting product value, access, and reimbursement decisions across global business units.
Senior Officer / Executive - Direct Procurement
Sun Pharmaceutical Industries Ltd
Mumbai2-5 Years · Onsite1 OctManage direct procurement of packaging materials for commercial sites and R&D locations, ensuring timely purchase orders, vendor coordination, delivery tracking, quality documentation, and procurement reporting.
Manager / Senior Manager - Medical Science Liaison
Eli Lilly and Company
Delhi NCR2-5 Years · Onsite1 OctField-based Medical Science Liaison role focused on Cardio-metabolic diseases, scientific exchange with healthcare experts, medical insights, strategic territory planning, and cross-functional collaboration.
Central Monitor Senior Associate
Amgen
Hyderabad2-5 Years · Onsite1 OctCentral Monitor Senior Associate independently performs proactive, data-driven central monitoring across clinical studies, using analytics and structured review to detect risks affecting patient safety, data quality, and protocol adherence.
Associate Project Specialist - Medical Communications
Sanofi
Hyderabad2-5 Years · Onsite30 SeptThis Associate Project Specialist – Medical Communications role at Sanofi in Hyderabad sits within Sanofi Business Operations (SBO), a centralized hub supporting Specialty Care, Vaccines, General Medicines, Consumer Healthcare, and R&D. The position is pivotal to delivering high-quality scientific publications and medical education materials—slide decks, abstracts, posters, and manuscripts—that communicate Sanofi’s clinical evidence to healthcare professionals, regulators, and payers. By coordinating project timelines, compliance submissions, budgets, and stakeholder communication, the specialist ensures scientific writers can focus on content excellence. This is an exceptional opportunity for life-sciences graduates to gain end-to-end exposure to medical publications, publication management tools like iEnvision and PromoMats, and global medical affairs operations. It offers a launchpad into medical writing, publications management, or scientific communications leadership within a top-tier pharmaceutical company.
Associate Quality Complaints
Amgen
Hyderabad2-5 Years · Onsite30 SeptOwn and execute quality complaint activities across the global complaint process, ensuring compliant handling, accurate records, timely closure, and appropriate escalation. The role connects customer feedback with quality processes and continuous improvement.
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Clinical Trial Support Specialist
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite30 SeptSupport end-to-end clinical trial submission operations by preparing submission-ready documents, maintaining clinical trial systems and data, coordinating regulatory milestones, and enabling efficient clinical development activities across the oncology portfolio.
ICN (Male)
AIMS India
Faridabad2-5 Years · Onsite30 SeptJoin AIMS India as an Infection Control Nurse (ICN) in Faridabad to drive hospital hygiene, patient safety, and clinical infection prevention standards.
Specialist, Quality Services – Product Complaints
Sanofi
Hyderabad2-5 Years · Onsite29 SeptSanofi's Global Manufacturing & Supply Services hub in Hyderabad is the operational backbone of the company's worldwide product quality agenda, and this Specialist Quality Services (Product Complaints) position sits at the frontline of post-market surveillance. The role owns intake, triage, categorization and closure of Product Technical Complaints across medical devices, pharmaceuticals, biologics and combination products — a workflow that directly protects patient safety and feeds the investigation, field alert and pharmacovigilance machinery of a 110,000-person life-sciences leader. Because Sanofi is investing heavily in AI-driven data standards and reusable quality data, specialists here gain exposure to modern QMS tooling and global cross-functional stakeholders. For an early-career quality professional, it is an exceptional launchpad: high regulatory visibility, structured GxP discipline and a clear route into broader quality, compliance and pharmacovigilance careers.
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Scientific Writer II
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite29 SeptScientific Writer II responsible for authoring and coordinating regulatory and clinical documents, integrating scientific, medical, and regulatory input while managing document strategy, review cycles, timelines, quality, and compliance.
Resident Medical Officer
HCG (Healthcare Global Enterprises)
Bangalore2-5 Years · Onsite29 SeptProvide emergency clinical care, manage patient records, and coordinate medical procedures as a Resident Medical Officer at HCG in Bangalore.
Jr. Officer - Production
Lupin
Goa2-5 Years · Onsite28 SeptManage pharmaceutical manufacturing, granulation, compression, and coating operations at Lupin in Goa.
Regulatory Affairs Associate II
Teva Pharmaceuticals
Mumbai2-5 Years · Onsite28 SeptRegulatory Affairs Associate II responsible for preparing, reviewing and submitting high-quality FDA regulatory submissions, managing post-approval change controls, maintaining regulatory databases and supporting ANDA annual reports and supplements.