Quality Assurance Job at Sanofi | Pharma Candidates Eligible – Apply
Looking for a Quality Assurance Job in the pharmaceutical industry? Sanofi Careers is hiring a Quality Assurance Specialist in Goa for professionals experienced in GMP compliance, quality systems, validation, documentation, and regulatory processes. This opportunity is suitable for B Pharm and M Pharm graduates looking to build their career in pharmaceutical quality assurance and contribute to maintaining high standards of product quality and patient safety.
- Job Title: Quality Assurance Specialist
- Location: Goa
About The Company
Sanofi is a global healthcare company dedicated to supporting people through their health challenges. Operating in the pharmaceutical sector, Sanofi focuses on developing innovative solutions to improve patient outcomes. The organization is committed to advancing science and enhancing the quality of life for individuals worldwide. Quality assurance jobs at Sanofi play a crucial role in maintaining high standards across its diverse product offerings.
Job Description
Sanofi is hiring for the position of Quality Assurance Specialist in Goa. This Quality Assurance Job involves managing pharmaceutical quality systems, ensuring GMP and GxP compliance, supporting validation activities, reviewing quality documents, and maintaining regulatory standards. The selected candidate will play a key role in ensuring product quality, documentation accuracy, and compliance with global pharmaceutical requirements.
Key Responsibilities
- Manage Quality Management Systems (QMS) including deviations, CAPA, change controls, and market complaint systems.
- Review and approve GxP documents, SOPs, Batch Manufacturing Records (BMR), and Batch Packing Records (BPR).
- Support OOS/OOT investigations, training management, and data integrity activities.
- Coordinate process validation, cleaning validation, transport validation, and computerized system validation.
- Manage Validation Master Plan (VMP), qualification activities, and quality documentation.
- Perform IPQA activities including line clearance, in-process checks, product sampling, and shop floor quality oversight.
- Support self-inspections, audits, regulatory compliance, and Site Master File (SMF) management.
- Conduct Nitrosamine Assessment, ICH Q3D compliance activities, audit trail reviews, and document control processes.
- Ensure compliance with GMP, GxP, HSE guidelines, and global quality standards.
Required Skills
- Strong knowledge of GMP and GxP compliance
- Experience with Quality Management Systems (QMS)
- Knowledge of CAPA, Change Control, and Deviation Management
- Understanding of Process Validation and Qualification activities
- Experience in Batch Record Review and Documentation Control
- Knowledge of IPQA operations and manufacturing quality oversight
- Understanding of Data Integrity, Audit Trail Review, and Regulatory Compliance
- Familiarity with ICH Q3D and Nitrosamine Assessment requirements
Eligibility Criteria
- Education: B.Pharm / M.Pharm
- Experience: 2–5 years of experience in pharmaceutical Quality Assurance, GMP compliance, validation, or quality systems.
This Quality Assurance Job at Sanofi provides an excellent opportunity for pharmacy professionals to advance their careers in pharmaceutical quality systems, validation, and regulatory compliance. Candidates interested in building their future through Sanofi Careers can apply for this role and become part of a global healthcare organization committed to quality, innovation, and patient safety.
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