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 76–100 of 515 jobs
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Manager I, Commercialization FP&A
Bristol Myers Squibb
Hyderabad5+ Years · Hybrid6 OctThe Manager I, Commercialization FP&A role supports financial planning and operational process management for BMS commercialization activities. The position focuses on forecasting, budgeting, management reporting, process improvement, governance, relationship management and business risk oversight.
Associate Manager Quality Control
Pfizer
Vizag5+ Years · Onsite6 OctThe Associate Manager Quality Control will perform analytical method validation, transfer and verification activities while supporting quality control testing and GMP compliance at Pfizer's Vizag location.
Senior Data Scientist – Surfaceome Biology
Amgen
Hyderabad5+ Years · Onsite6 OctAmgen is hiring a Senior Data Scientist – Surfaceome Biology in Hyderabad to develop computational and AI/ML approaches for integrating biomedical data and supporting target discovery, validation, biomarker development, and therapeutic research.
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.
Sr. Specialist LCoE Operations
Regeneron
Hyderabad5+ Years · Hybrid6 OctRegeneron is hiring a Senior Specialist Learning Center of Excellence Operations in Hyderabad to support regional training, onboarding and learning delivery for its India Global Capabilities Center. The role involves training content development, facilitation, Learning Management System administration, onboarding coordination and collaboration with regional and global stakeholders.
Upstream Field Application Scientist
Merck
Mumbai5+ Years · Onsite6 OctMerck is hiring an Upstream Field Application Scientist in Mumbai to provide technical expertise and customer support for upstream bioprocessing and biomanufacturing solutions. The role focuses on process development, scale-up, implementation studies, technical training and customer engagement across process materials, cell culture and upstream platform solutions.
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.
Quality Expert, Data Analytics and Statistical Support
Lonza
Hyderabad5+ Years · Hybrid5 OctLonza is hiring a Quality Expert for Data Analytics and Statistical Support in Hyderabad to oversee manufacturing consistency and compliance through statistical analysis. The role involves managing control charting, supporting root-cause investigations, and generating reports for Periodic Quality Review and Continued Process Verification.
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.
Global Regulatory Affairs Labelling Group Lead
Sanofi
Hyderabad5+ Years · Hybrid5 OctThis Global Regulatory Affairs (GRA) Labelling Group Lead role at Sanofi in Hyderabad is a senior people-leadership and labeling strategy position within one of the world’s leading biopharmaceutical companies. It owns the end-to-end creation, maintenance, and negotiation of corporate labeling documents—CCDS, US Prescribing Information, EU SmPC, WHO labeling, and patient leaflets—across a large portfolio of marketed, lifecycle-management, and development products. The position is pivotal to Sanofi’s ability to secure and maintain marketing authorizations, respond to health authority queries, and deliver compliant, competitive labels that support patient safety and commercial success. For experienced regulatory professionals, this is a rare opportunity to shape global labeling strategy, lead multidisciplinary teams, and influence senior governance committees while working in a hybrid, high-impact environment.
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.
Senior Clinical Trial Manager (Sr. CTM) - Internal Medicine
Thermo Fisher Scientific
Mumbai5+ Years · Remote5 OctSenior Clinical Trial Manager role responsible for end-to-end clinical trial start-up and clinical deliverables for moderate-to-high complexity studies within Internal Medicine and related therapeutic areas.
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.
Senior Global Regulatory Affairs Labeling Specialist
Sanofi
Hyderabad5+ Years · Hybrid4 OctThis Senior GRA Labeling Specialist role at Sanofi in Hyderabad is a strategic regulatory affairs position responsible for shaping corporate labeling documents such as CCDS, USPI, and EU SmPC across marketed and lifecycle products. Labeling is the final, legally binding communication of a medicine's benefit-risk profile, directly impacting patient safety and commercial viability. The incumbent will chair multidisciplinary labeling working groups, lead agency negotiations, and ensure alignment with global regulatory strategy. As Sanofi advances its pipeline in immunology, oncology, rare diseases, and vaccines, this role offers a high-visibility opportunity to influence product approvals, lifecycle extensions, and competitive differentiation. Working in a hybrid model, the specialist will collaborate with global pharmacovigilance, medical affairs, and legal teams, making it an ideal next step for an experienced labeling professional seeking global impact.
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.
Senior Manager, Clinical Operations (FSP)
Thermo Fisher Scientific
Remote5+ Years · Remote4 OctSenior clinical operations leadership role responsible for managing clinical operations staff, FSP client relationships, resource allocation, performance management, quality, training and operational delivery across clinical trials.
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).