Sanofi, a leading global biopharmaceutical company, is hiring a Quality Assurance Specialist in Goa (Verna Industrial Estate, Salcete). This is an excellent opportunity for B.Pharm / M.Pharm professionals with 2–5 years of experience in pharmaceutical Quality Assurance (QA), QMS, IPQA, and Validation systems.
If you are looking to build your career in pharmaceutical Quality Assurance jobs in Goa, this Sanofi QA Specialist role offers exposure to GMP compliance, product quality reviews, deviation management, validation oversight, and batch release activities in a reputed multinational pharmaceutical company.
📌 Job Overview
- Position: Quality Assurance Specialist
- Location: Goa Site, Verna Industrial Estate, Salcete, India
- Experience: 2–5 Years
- Qualification: B.Pharm / M.Pharm
- Languages Preferred: English, Hindi, Konkani, Marathi
- Application Deadline: April 1, 2026
This Sanofi QA Specialist job in Goa focuses on managing Quality Management Systems (QMS), change controls, CAPA, deviation systems, IPQA activities, validation, and data integrity compliance.
🔬 Key Responsibilities – Quality Assurance Specialist
1️⃣ Quality Systems & QMS Management
- Management of Product Quality Reviews (PQR)
- Handling Change Control & Deviation systems
- Oversight of Market Complaint investigations
- OOS/OOT management
- CAPA system implementation and closure
- Nitrosamine assessment & ICH Q3D compliance
- Implementation of Sanofi Global Standards (STDs) & GOPs
- Subcontractor & service provider QA oversight
2️⃣ GMP & Documentation Control
- Review & approval of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
- GxP document review & SOP control
- Site Master File (SMF) handling
- Audit trail review & data integrity management
- User access management & document archival
3️⃣ Validation & Qualification
- Process, cleaning, transport & computerized system validation
- Temperature & humidity mapping
- Hold time studies & utilities validation
- Management of Qualification & Validation Master Plan
4️⃣ In-Process Quality Assurance (IPQA)
- Line clearance in production
- In-process checks & shopfloor oversight
- Sampling during routine production & validation
- Logbook review & master batch record approval
5️⃣ HSE & Compliance
- Ensuring cGMP & HSE adherence
- Conducting safety training & QDCI meetings
- Promoting zero LTI (Lost Time Injury) culture
This role is ideal for professionals seeking pharmaceutical QA jobs in Goa with GMP, IPQA, and validation exposure.
🎓 Qualifications & Skills Required
- B.Pharm or M.Pharm (mandatory)
- 2–5 years of experience in:
- Quality Assurance (QA)
- QMS & GMP documentation
- Deviation, CAPA, Change Control
- Validation & Qualification
- IPQA activities
- Data Integrity & Audit Trail Review
Strong knowledge of ICH guidelines, GMP compliance, regulatory standards, and pharmaceutical manufacturing processes is essential.
💼 Why Join Sanofi?
Working at Sanofi offers:
- Exposure to global pharmaceutical quality standards
- Experience in multinational regulatory compliance
- Structured training & career progression
- Inclusive & diversity-driven workplace
- Competitive compensation & benefits
Sanofi provides equal employment opportunities and promotes diversity, equity, and inclusion across its global operations.
💰 Salary (Estimated)
For a Quality Assurance Specialist with 2–5 years experience in Goa, the expected salary range is:
₹5,50,000 – ₹8,50,000 per annum (CTC)
(Salary may vary based on experience and internal company structure.)
📍 How to Apply
