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 48 jobs
Team Lead – Global Regulatory Affairs Labelling Strategist
Sanofi
Hyderabad5+ Years · HybridTodaySanofi's Global Regulatory Affairs (GRA) labelling organization is the function that shapes the Company Core Data Sheet (CCDS), US Prescribing Information, EU SmPC and patient leaflets that govern how every Sanofi medicine is described to physicians, regulators and patients worldwide. As Team Lead GRA Labelling Strategist in Hyderabad, the incumbent owns both a portfolio of products and a team of labelling strategists, converting clinical study reports, pharmacovigilance signals and competitive intelligence into approved labelling text. The role sits at the crossroads of regulatory strategy, drug safety and medical affairs, making it one of the most visible scientific-commercial positions in the company. Because labelling decisions directly unlock new indications, line extensions and marketing authorizations across the US, EU and WHO markets, this position offers exceptional exposure to senior executive governance and long-term career capital.
Senior Analyst, Enterprise Competitive Intelligence
Novartis
Hyderabad5+ Years · Hybrid3 days agoNovartis is hiring a Senior Analyst, Enterprise Competitive Intelligence in Hyderabad on a hybrid basis. The role involves competitive intelligence analysis across brands, franchises and therapy areas, supporting clinical, commercial and regulatory strategy discussions.
Team Lead - Global Regulatory Affairs Labeling Strategist
Sanofi
Hyderabad5+ Years · Hybrid6 days agoThis senior leadership position sits within Sanofi's Global Regulatory Affairs Labeling (GRAL) function in Hyderabad, shaping the corporate core data sheets (CCDS), US Prescribing Information, EU SmPC and WHO labeling that govern how Sanofi's medicines are described worldwide. Labeling strategy is the final gatekeeper of a medicine's approved claims — every safety signal, new indication or line extension must be translated into defensible regulatory text. As Team Lead, you will chair multidisciplinary labeling working groups, defend proposals before the Labeling Governance Committee, and represent Sanofi in Health Authority negotiations across EU and US procedures. Because labeling decisions directly unlock or restrict commercial claims, this role enjoys exceptional visibility with senior executive management and offers a rare blend of scientific depth, cross-functional influence and people leadership inside one of the world's largest pharmaceutical companies.
RLT Dosimetry Data Flow Expert
Novartis
Hyderabad0-2 Years · Hybrid7 days agoNovartis is recruiting an RLT Dosimetry Data Flow Expert in Hyderabad to manage and review dosimetry, imaging, gamma-counting, radiometabolite and pharmacokinetic data across radioligand therapy studies. The position involves dataset reconciliation, discrepancy resolution and coordination with study teams, internal functions and external partners.
Direct Materials Life Cycle Manager
Novartis
Hyderabad5+ Years · Hybrid9 days agoNovartis is hiring a Direct Materials Life Cycle Manager in Hyderabad to lead supplier introduction and direct materials projects for the Small Molecules platform. The job focuses on excipients and chemicals, project delivery, and compliance with quality, regulatory and GMP requirements.
Senior Manager – Commercial Forecasting & Analytics
Amgen
Hyderabad5+ Years · Hybrid10 days agoAmgen is recruiting a Senior Manager for Commercial Forecasting & Analytics in Hyderabad to lead forecasting work for global and U.S. commercial teams. The position combines individual forecasting work with team oversight and cross-regional collaboration.
Global QMS Manager
Novartis
Hyderabad2-5 Years · Hybrid27 days agoNovartis is hiring a Global QMS Manager in Hyderabad to oversee compliance and governance of Batch Release Hub configurations and related quality systems. The role works across Quality, IT and business teams on system changes, validation, documentation and global user support.
Transition Manager Quality
Lonza
Hyderabad5+ Years · Hybrid6 OctLonza is hiring a Transition Manager Quality in Hyderabad to lead the transfer and improvement of Quality processes into its Global Capability Center. The role requires extensive BioPharma, pharmaceutical manufacturing, or CDMO experience with hands-on GMP-regulated Quality experience.
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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.
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.
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.
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.
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.
Senior Manager Medical Review
Regeneron
Hyderabad5+ Years · Hybrid3 OctLead medical review and case-quality activities for global pharmacovigilance programs in a hybrid Hyderabad role, ensuring safety cases are scientifically sound, compliant, and inspection-ready.
Clinical Evaluation Medical Writer
Medtronic
Hyderabad5+ Years · Hybrid2 OctClinical Evaluation Medical Writer responsible for developing and maintaining clinical evaluation and regulatory documents that support the safety, performance, reliability, and regulatory compliance of medical devices.
Senior Regulatory Affairs Specialist
Medtronic
Hyderabad5+ Years · Hybrid2 OctSenior Regulatory Affairs Specialist responsible for regulatory strategy, submissions, regulatory information management, compliance assessments, and global product registrations. The role supports medical-device and/or pharmaceutical regulatory activities and collaborates with business and international regulatory teams.
Sr Regulatory Consultant (CMC, EU mkt) (Office based)
Syneos Health
Hyderabad5+ Years · Hybrid2 OctLead and contribute to regulatory consulting projects with a strong focus on CMC regulatory strategy, EU market requirements, post-approval variations, lifecycle management, and regulatory submissions for pharmaceutical products.
Senior Scientific Writer - HEVA
Sanofi
Hyderabad5+ Years · Hybrid1 OctSanofi, a global leader in healthcare, is seeking a Senior Scientific Writer for its Health Economics and Value Assessment (HEVA) team at the Sanofi Global Hub in Hyderabad. This role is pivotal in communicating the value of Sanofi's pharmaceutical portfolio to global stakeholders, including payers, healthcare professionals, and regulatory bodies. By creating high-impact scientific publications and HEVA communication deliverables, you will directly influence access and reimbursement decisions, ultimately ensuring patients receive life-changing therapies. This position offers a unique opportunity to work at the intersection of science, health economics, and medical communications, collaborating with cross-functional teams across R&D, Medical Affairs, and Market Access. If you are passionate about translating complex HEVA evidence into compelling narratives and want to grow your career in a dynamic, innovation-driven environment, this role at Sanofi is an exceptional platform.
Mgr, Regulatory Consulting (Office based)
Syneos Health
Hyderabad2-5 Years · Hybrid1 OctManager, Regulatory Consulting leads regulatory consulting projects, regulatory submissions, client engagements, project teams, and people-management activities while providing strategic and operational regulatory advice across pharmaceutical and related product development programs.
Regulatory Intelligence Senior Specialist
Lonza
Hyderabad5+ Years · Hybrid29 SeptDrive global regulatory intelligence surveillance and analysis across human and veterinary medicines, translating changing health authority requirements into actionable insights that support compliance, risk management, and Lonza's global CDMO operations.
Regulatory Intelligence Senior Specialist
Lonza
Hyderabad5+ Years · Hybrid29 SeptRegulatory Intelligence Senior Specialist responsible for global regulatory surveillance, impact assessment, regulatory trend analysis, stakeholder collaboration, intelligence reporting, dashboards, and regulatory risk identification across human and veterinary medicines.
Manager, Clinical Operations
Syneos Health
Hyderabad5+ Years · Hybrid29 SeptLead clinical operations teams at Syneos Health in Hyderabad, overseeing site activations, monitoring, and regulatory submissions.
Clinical Monitoring (CM)
Syneos Health
Hyderabad2-5 Years · Hybrid29 SeptSupport clinical trial oversight through independent monitoring, patient-level data review, study and site-level trend analysis, risk identification, and risk-based quality management.
Site Start Up EUCTR II
Parexel
Hyderabad2-5 Years · Hybrid26 SeptSupport complex clinical trial initiation, focusing on EU CTR compliance and CTIS database management.
Associate Director - Strategic Resource Planning
Amgen
Hyderabad5+ Years · Hybrid26 SeptAmgen's Operations Strategy & Business Resilience (OSBR) group functions as an internal management-consulting arm for the company's global manufacturing and supply organisation. This Associate Director role anchors the Amgen India (AIN) delivery hub in Hyderabad, translating demand from California-based leadership into prioritised, decision-ready analytics. The position matters because Amgen's biotechnology pipeline — biologics, biosimilars and next-generation medicines — depends on drug substance and drug product networks that must be modelled, stress-tested and capacity-planned years ahead. Leading eight to ten managers, the Associate Director ensures business cases, scenario models and network capacity analyses reach executive-grade quality. For seasoned pharma operations leaders, it is a rare opportunity to shape a greenfield capability centre while remaining close to global supply-chain strategy.