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 51–75 of 323 jobs
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.
Full Stack Engineer – Biologics Discovery Platform
AstraZeneca
Chennai5+ Years · Onsite5 OctAstraZeneca's Global Capability Centre in Chennai is hiring a Full Stack Engineer to build the Augmented Biologics Discovery Platform — a cloud-native product suite that shortens the path from antibody idea to clinical candidate. Sitting at the intersection of software engineering, AI/ML and computational biology, the role translates complex scientific workflows into production-grade services and data products that discovery scientists use every day. This is a strategic build-out for AstraZeneca: biologics represent a fast-growing share of its oncology, respiratory and rare-disease pipeline, and the speed at which computational teams can model, rank and validate antibody candidates directly influences how quickly programmes reach IND. For engineers who want their code to shape real therapeutic programmes rather than generic enterprise software, it is a rare opportunity to work beside scientists, product leaders and MLOps specialists at global scale.
Team leader-Visual inspection
Pfizer
Vizag5+ Years · Onsite5 OctTeam Leader responsible for visual inspection activities within Pfizer's pharmaceutical manufacturing operations in Vizag.
MSL Oncology West
Bayer
Thane0-2 Years · Onsite5 OctMedical Science Liaison role focused on Oncology, scientific exchange, thought-leader engagement, clinical research support and medical education.
Clinical Data QC Reviewer
Sanofi
Hyderabad5+ Years · Onsite4 OctThis Clinical Data QC Reviewer role at Sanofi Business Operations in Hyderabad sits at the heart of clinical data integrity for registry and real-world evidence studies. As Sanofi centralizes global medical, HEVA, and commercial support, this position ensures eCRF, EDC, and SAS listings meet rigorous quality control standards before they inform regulatory submissions, publications, or safety decisions. The reviewer will work with Medidata RAVE and cross-functional stakeholders to validate data, manage issues, perform UAT, and uphold GCP, FDA, EMA, and ICH expectations. It is a compelling opportunity for experienced clinical data professionals to deepen therapeutic and systems expertise, contribute to Sanofi’s Specialty Care, Vaccines, and General Medicines pipeline, and influence process improvements in a global, science-driven environment.
Associate Manager - Automation
Pfizer
Visakhapatnam5+ Years · Onsite4 OctPfizer’s Vizag manufacturing site plays a critical role in producing essential medicines for global markets. As Associate Manager – Automation, you will be the technical owner of process control systems—DeltaV DCS, SCADA, and PLCs—that keep production lines reliable, compliant, and efficient. This role sits at the intersection of engineering, validation, and regulatory compliance, ensuring automation systems meet 21 CFR Part 11, cGAMP, and GMP expectations. You will support investigations, audits, periodic reviews, and capital projects, directly impacting Pfizer’s ability to deliver medicines without interruption. For experienced automation engineers seeking a purpose-driven career, this position offers deep exposure to pharmaceutical manufacturing, cross-functional collaboration, and the chance to shape site automation standards. It is an ideal move for professionals who want to combine hands-on technical work with meaningful patient impact.
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.
Quality Specialist (QMS, Documentation)
Merck
Bangalore5+ Years · Onsite4 OctQuality Assurance Specialist responsible for maintaining the Quality Management System, leading quality activities, ensuring regulatory compliance, and strengthening product and process quality within Merck's Life Science division in India.
Medical Science Liaison
Bayer
Hyderabad0-2 Years · Onsite4 OctMedical Science Liaison role focused on scientific exchange, medical education and engagement with healthcare professionals, thought leaders, medical societies and advisory boards within an assigned therapeutic area.
Director, Global Clinical Trial Services, India
Regeneron
Hyderabad5+ Years · Onsite4 OctSenior operational leadership role responsible for clinical trial delivery across India, from feasibility through site close, while ensuring compliant execution, strong vendor performance, effective resource planning, and alignment with global clinical development standards.
Associate Manager - Quality Compliance
Pfizer
Vizag5+ Years · Onsite3 OctAssociate Manager responsible for Quality Compliance, Data Integrity, Market Complaints, investigations, CAPA and quality systems within a regulated pharmaceutical manufacturing environment.
Senior Manager - Medical & Scientific Affairs
Roche
Mumbai5+ Years · Onsite3 OctLead medical strategy and scientific engagement for Roche Diagnostics India's cardiology and neurology solutions, driving evidence generation, HCP/KOL engagement, and compliant medical activities.
Expert - Regulatory Labelling Operations
Merck KGaA
Bangalore5+ Years · Onsite3 OctThe Expert - Regulatory Labelling Operations role focuses on global labeling operational excellence, process optimization, compliance tracking and continuous improvement within Regulatory Quality Safety (RQS).
Assistant Manager, Clinical Data Management
Teva Pharmaceuticals
Bangalore5+ Years · Onsite2 OctLeads and supports Clinical Data Management delivery with subject matter expertise, study oversight, quality control and process improvement. The role combines technical CDM expertise with resource coordination, mentoring, standards development and audit support.
Senior Scientific Writer – Health Economics and Value Assessment (HEVA)
Sanofi
Hyderabad5+ Years · Onsite2 OctSenior scientific writing role focused on Health Economics and Value Assessment communications. The position develops high-quality HEVA evidence communications and supports global access, reimbursement and scientific communication strategies across Sanofi.
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.
Group Lead - Scientific Writing
Sanofi
Hyderabad5+ Years · Onsite2 OctLeads a multi-layered scientific writing organization supporting pharmaceutical and healthcare content across therapeutic areas. Drives scientific quality, publication and medical education deliverables, stakeholder engagement, technology adoption and operational efficiency.
- B
Negotiation Governance Lead, Site Contracting
Bristol Myers Squibb
Hyderabad5+ Years · Onsite2 OctLead complex clinical trial site contract and budget negotiations, governance, escalations and process improvements for BMS-sponsored research. The role provides strategic oversight, negotiation expertise, training and quality governance across global clinical contracting operations.
Artwork Reviewer - Global Artwork
Amgen
Hyderabad0-2 Years · Onsite2 OctArtwork Reviewer responsible for reviewing pharmaceutical product artworks, templates, supplier print proofs, and partner-generated artwork while ensuring compliance with Amgen procedures and quality requirements.
Clinical Development Scientist
Novartis
Hyderabad0-2 Years · Onsite2 OctClinical Development Scientist / Clinical Scientific Expert I supporting global clinical trials through clinical data review, scientific insight generation, data quality oversight, study documentation, and cross-functional trial activities. The role contributes to delivering clinical study outcomes within schedule, budget, quality, compliance and performance standards.
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.
Pharmacist
Prashanth Group of Hospitals
Padur0-2 Years · Onsite1 OctManage hospital pharmacy operations, dispense medications accurately, and ensure strict compliance with pharmaceutical guidelines.
Medical Writing Specialist
Novo Nordisk
Bangalore5+ Years · Onsite1 OctSenior medical writing specialist role responsible for leading clinical reporting deliverables, setting direction for complex medical writing work, coordinating global stakeholders, and driving quality and process improvements across clinical development programmes.
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 Clinical Research Associate II
Pfizer
Mumbai5+ Years · Onsite1 OctLead and support moderately complex clinical research projects, overseeing study startup, monitoring plans, regulatory activities, budgets, drug supply, and site-level execution for pharmaceutical clinical studies.