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16 October 2026

Apply Online for Senior Manager at Bristol Myers Squibb

The QPPV support team is headed by the QPPV (EEA & UK QPPV) and is an expert interface for regulatory and scientific requirements and build the interface between Local/Regional safety regulatory environment and Global product Teams, both in development and post-marketing.
16 October 2026

Apply Online for Associate Data Manager at Medpace

Bachelors degree with clinical Data Management experience, including managing multiple clinical projects and serving as the primary sponsor contact.
16 October 2026

Require Associate Pharmacovigilance Manager at Novo Nordisk

Responsible for leading and overseeing local pharmacovigilance activities, including adverse event case processing, safety reporting to Health Authorities, customer complaint handling, regulatory compliance, data quality, and stakeholder collaboration across clinical development and post-marketing activities.
16 October 2026

Work as Safety Data Sheets Expert at Sanofi

Bachelors degree in Biological Science (biology, microbiology, Molecular Biology) or technical discipline at minimum.
16 October 2026

GSK looking for Senior Scientist Pharmacovigilance

Experience in Pharmacovigilance and Medical Information regulatory requirements, systems, and processes
15 October 2026

HETERO IS HIRING | FRESHERS – REGULATORY AFFAIRS

HETERO is looking for enthusiastic, detail-oriented, and motivated freshers to join our Regulatory Affairs Team in Hyderabad.
15 October 2026

Vacancy for MPharm, MSc in Analytical R&D Lab at FDC Limited

Good knowledge in analytical instrumentation commonly used in pharmaceutical testing such as HPLC, UV, Dissolution, FTIR and Karl-Fisher.
15 October 2026

Apply Online for Regulatory Affairs Manager at IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Post : Regulatory Affairs, Manager
15 October 2026

Apply Online for Production Specialist at WIPRO

Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner. Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue
15 October 2026

Cognizant Hiring Pharmacovigilance Specialist

Preferred certifications include pharmacovigilance or drug safety training from recognized industry bodies such as DIA or similar professional organizations.