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Quality Assurance Specialist
Sanofi
Goa (Verna)
2–5 Years
GMP & QMS
IPQA & Validation
₹5.5–8.5 LPA
🏢 About Sanofi
Sanofi is a global biopharmaceutical company committed to improving patient lives through innovative medicines and high-quality manufacturing standards. The Goa facility operates under global GMP and regulatory compliance frameworks.
📌 Job Overview
- Position: Quality Assurance Specialist
- Location: Verna Industrial Estate, Goa
- Experience: 2–5 Years
- Qualification: B.Pharm / M.Pharm
- Languages Preferred: English, Hindi, Konkani, Marathi
- Application Deadline: April 1, 2026
🔬 Key Responsibilities
- Manage Product Quality Reviews (PQR)
- Handle Change Control, Deviations & CAPA systems
- Investigate market complaints & OOS/OOT cases
- Ensure compliance with ICH Q3D & nitrosamine assessments
- Review Batch Manufacturing & Packing Records
- Control SOPs & GxP documentation
- Manage data integrity & audit trail reviews
- Oversee validation & qualification activities
- Perform line clearance & in-process quality checks
- Ensure cGMP & HSE compliance
🧪 Validation & IPQA Oversight
- Process & cleaning validation
- Temperature & humidity mapping
- Utilities & transport validation
- Hold time studies & qualification plans
- Sampling during production & validation
🎓 Qualifications & Skills
- B.Pharm or M.Pharm (Mandatory)
- Experience in QA, GMP & QMS systems
- Deviation, CAPA & Change Control handling
- IPQA & validation experience
- Knowledge of ICH guidelines & regulatory standards
- Understanding of pharmaceutical manufacturing processes
⭐ Why Join Sanofi?
- Exposure to global GMP & compliance systems
- Work in a multinational pharma environment
- Structured career growth & training
- Inclusive & diversity-driven workplace
- Competitive compensation & benefits
📌 Note Before You Apply:
Candidates with strong GMP, QMS, IPQA, and validation experience will have a competitive advantage.
Candidates with strong GMP, QMS, IPQA, and validation experience will have a competitive advantage.
👇 Apply Online 👇
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