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Pfizer, a global leader in healthcare innovation, is hiring Associate II – Labeling Operations in Chennai, India. This role offers a unique opportunity to ensure pharmaceutical product labels meet global regulatory requirements, helping healthcare professionals and patients receive accurate and safe product information. With 0–2 years of experience, this is a golden entry point into regulatory affairs for aspiring life science professionals.
Key Responsibilities
As Associate II – Labeling Operations, you will:
- Generate, edit, and finalize labeling documents in GDMS.
- Manage labeling workflows, ensuring compliance with SOPs and regulatory standards.
- Consolidate and version-control labeling documents.
- Prepare comparison tables and integrate reviewer feedback.
- Coordinate timely reviews, approvals, and document updates.
- Maintain CDS logs and project tracking systems.
- Support cross-functional teams including Regulatory Affairs and Drug Listing.
Minimum Qualifications
- Bachelor’s degree in science or life sciences (B.Pharm, M.Pharm, B.Sc., M.Sc. preferred).
- 0–2 years of relevant experience.
- Proficiency in Microsoft Office Suite.
- Basic understanding of regulatory labeling requirements.
- Strong organizational, communication, and attention-to-detail skills.
- Ability to manage multiple tasks and work independently.
Preferred Qualifications
- Experience in the pharmaceutical/biotechnology industry.
- Familiarity with labeling software and electronic document management systems.
- Knowledge of global labeling regulations.
- Strong interpersonal and analytical skills.
- Problem-solving abilities in regulatory contexts.
Benefits
- Work with a global pharmaceutical leader.
- Gain exposure to international regulatory frameworks.
- Opportunity for career growth in Regulatory Affairs.
- Collaborative and inclusive work environment.
Application Process
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