Roles and Responsibilities

- Ensure compliance with regulatory requirements, company policies, and procedures related to quality assurance (QA) and quality management system (QMS).

- Conduct stability studies on pharmaceutical products according to established protocols and guidelines.

- Review and approve batch manufacturing records (BMRs), test results, and other documentation for accuracy and completeness.

- Collaborate with cross-functional teams to resolve issues related to product quality, process validation, or equipment calibration.

- Maintain accurate records of all activities performed during the shift operation.

- 3-8 years of experience in QA/QMS Document Cell Stability IPQA role.
- Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from a recognized institution.
- Strong understanding of Good Manufacturing Practices (GMP), Current Valuable Laboratory Practice (cGMP), Quality Assurance principles, and Quality Management System (QMS).
- Proficiency in preparing documents such as BMRs, stability protocols, test reports using software like LIMS/Lotus Notes/Word/Excel etc.

📌 Walk in Interview @ Vadodara For QA QMS Doc cell Stability IPQA (Gujarat)
🏢 Intas
📍 Gujarat