💼 Pfizer Associate II – Labeling Operations (Freshers)
🏢 Company: Pfizer📍 Location: Chennai, India
🎓 Eligibility: B.Pharm, M.Pharm, B.Sc., M.Sc. preferred
🧪 Experience: 0–2 Years
📝 Job Type: Full-Time | Regulatory Affairs | On-site
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🏢 About Pfizer
Pfizer is a global leader in healthcare innovation, dedicated to discovering, developing, and delivering quality medicines that make a difference in people’s lives. With a strong focus on research and regulatory compliance, Pfizer’s work ensures healthcare professionals and patients receive safe, effective, and accurate product information.
📌 Key Responsibilities
- ✔ 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.
✅ Eligibility & Skills
- ✅ 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.
🎁 Why Join Pfizer?
- 🌐 Work with a global pharmaceutical leader.
- 📈 Gain exposure to international regulatory frameworks.
- 💼 Opportunity for career growth in Regulatory Affairs.
- 🤝 Collaborative and inclusive work environment.
📌 Note Before You Apply:
Highlight your understanding of regulatory labeling processes, proficiency in Microsoft Office, and ability to work with cross-functional teams. Showcase any experience or knowledge related to labeling software and regulatory standards.
👇 Application Link Will Be Visible in 15 Seconds 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
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