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Opella HealthCare Hiring For Jr. Scientific Writer & Pharmacovigilance Roles
📍 Location: Hyderabad
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, MBBS, MD, Lifesciences
🧾 Job Type: Full-Time | On-site
💼 Experience: 0 - 4 Years
🌐 About Company:
Opella is a division of Sanofi, globally recognized in self-care and OTC healthcare with iconic brands like Allegra, Dulcolax, and Buscopan. With 11,000+ employees, 13 manufacturing sites, and 4 global innovation centers, Opella aims to make healthcare simpler, inclusive, and accessible. As a certified B Corp, they are committed to sustainability, innovation, and ethical practices in healthcare.
Opella is a division of Sanofi, globally recognized in self-care and OTC healthcare with iconic brands like Allegra, Dulcolax, and Buscopan. With 11,000+ employees, 13 manufacturing sites, and 4 global innovation centers, Opella aims to make healthcare simpler, inclusive, and accessible. As a certified B Corp, they are committed to sustainability, innovation, and ethical practices in healthcare.
📝 Job Openings at Opella – Hyderabad:
Requisition ID: R2799591
Last Date to Apply: July 31, 2025
Responsibilities:
Requisition ID: R2804114
Last Date to Apply: August 31, 2025
Responsibilities:
Requisition ID: R2804117
Last Date to Apply: August 5, 2025
Responsibilities:
Eligibility:
1️⃣ Junior Scientific Writer
Location: HyderabadRequisition ID: R2799591
Last Date to Apply: July 31, 2025
Responsibilities:
- Create and edit medical content – manuscripts, slide decks, abstracts.
- Support publication plans, med-ed materials and scientific presentations.
- Coordinate with cross-functional teams and medical experts.
- Use platforms like PromoMats, iEnvision for documentation compliance.
- M.Pharm, PharmD, MBBS or Life Sciences Master’s Degree
- 0-2 years in medical/scientific writing
- Excellent English writing and analytical skills
2️⃣ Pharmacovigilance Case MR Oversight Specialist
Location: HyderabadRequisition ID: R2804114
Last Date to Apply: August 31, 2025
Responsibilities:
- Perform medical review of ICSRs (Individual Case Safety Reports)
- Maintain data integrity in PV databases like Aris-G, ARGUS
- Support Risk Management Plans, Signal Detection, and Regulatory Submissions
- Ensure compliance with global PV guidelines (FDA, EMA, ICH-GVP)
- MBBS/MD/PharmD
- 2-3 years in medical review of safety reports
- Familiarity with PV software, signal evaluation, causality assessment
3️⃣ Pharmacovigilance Product & Regulatory Associate
Location: HyderabadRequisition ID: R2804117
Last Date to Apply: August 5, 2025
Responsibilities:
- Configure product rules in safety databases
- Ensure regulatory compliance across countries via collaboration with QPPV offices
- Maintain label documents in Veeva Vault
- B.Pharm, M.Pharm or Life Science graduate with 3-4 years of PV experience
- Experience in ARGUS, Veeva Vault, Aris-G
- Good knowledge of international PV regulations
🌟 Why Join Opella?
✅ Work on Global Safety & Medical Writing Projects
✅ Be Part of a B Corp Certified Ethical Company
✅ Opportunities to Grow in Regulatory & Scientific Domains
✅ Collaborative & Inclusive Environment with Training Support
📩 Application Link:
📌 Note Before You Apply:
We use a 15-second timer to encourage you to read the job description carefully before applying. Understanding the role increases your chances of success and helps create a strong impression.
✅ Work on Global Safety & Medical Writing Projects
✅ Be Part of a B Corp Certified Ethical Company
✅ Opportunities to Grow in Regulatory & Scientific Domains
✅ Collaborative & Inclusive Environment with Training Support
📩 Application Link:
📌 Note Before You Apply:
We use a 15-second timer to encourage you to read the job description carefully before applying. Understanding the role increases your chances of success and helps create a strong impression.
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