Pfizer Pharmacovigilance Jobs – Senior Associate, Peer QC Analyst

Pfizer Recruitment – Senior Associate, Peer QC Analyst

About Pfizer

Pfizer is a global leader in biopharmaceutical innovation, dedicated to discovering, developing, and delivering healthcare solutions that improve patient outcomes. With a strong commitment to pharmacovigilance, Pfizer ensures the safety and efficacy of its pharmaceutical products through rigorous compliance with global safety regulations.

Are you an experienced pharmacovigilance professional looking to elevate your career? Pfizer is hiring a Senior Associate, Peer QC Analyst for its Chennai, India location. If you have expertise in Individual Case Safety Reports (ICSR) processing or aggregate reporting, this could be the ideal opportunity for you!

Job Overview – Senior Associate, Peer QC Analyst

Current Vacancies:

• Position: Senior Associate, Peer QC Analyst
• Department: Pharmacovigilance – Aggregate Safety Report Quality Control
• Location: Chennai, India
• Experience Required: Minimum 2 years in clinical, safety, or regulatory areas in the pharmaceutical industry, preferably in ICSR processing or aggregate report QC (PADER, PSUR, DSUR)
• Qualification: BS degree in Life Sciences, Nursing, Pharmacy, or related fields
• Work Mode: Hybrid

Key Responsibilities

Aggregate Report Quality Control & Compliance

• Conducts and manages Quality Control (QC) activities for Aggregate Safety Reports such as PADER, PSUR, and DSUR.
• Ensures compliance with global regulatory requirements and internal safety reporting standards.
• Reviews and verifies safety data for consistency, accuracy, and compliance.
• Supports internal audits and regulatory inspections.

Collaboration & Process Improvement

• Participates in and leads peer QC activities within the Aggregate Report Center of Excellence (CoE).
• Collaborates with cross-functional teams to enhance safety reporting accuracy.
• Contributes to process improvement initiatives for QC operations.

Documentation & Training

• Documents peer QC findings, trends, and compliance metrics.
• Serves as a Subject Matter Expert (SME) for training and process enhancement.
• Provides guidance on best practices in pharmacovigilance quality control.

Required Qualifications

Education Background

Candidates should have a BS degree in:

• Life Sciences (e.g., Biotechnology, Microbiology, Biochemistry, Molecular Biology, Genetics)
• Pharmacy (B. Pharm, M. Pharm, Pharmaceutical Sciences)
• Nursing (B.Sc Nursing, M.Sc Nursing, Clinical Research Nursing)
• Medical or Healthcare-related fields (Biomedical Sciences, Public Health, Toxicology)

Experience & Technical Skills

• Minimum 2+ years in pharmacovigilance, safety, or regulatory roles within the pharmaceutical industry.
• Strong knowledge of case processing (ICSR) and aggregate reports (PADER, PSUR, DSUR).
• Familiarity with global pharmacovigilance regulations and industry guidelines.
• Proficiency in data analysis, quality control, and compliance audits.
• Strong communication and collaboration skills.

How to Apply

Ready to take the next step in your pharmacovigilance career? Click the link below to apply:

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