Key Responsibilities
- Conduct process validation, cleaning validation, sterilization, and injectable processing activities according to cGMP guidelines.
- Ensure compliance with regulatory requirements for pharmaceutical manufacturing facilities.
- Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.
- Develop and maintain documentation related to production processes, equipment qualification, and batch records.
- Participate in audits conducted by regulatory agencies or internal stakeholders.
Educational Qualification
- MS/M.Sc(Science)/M.Pharma/B.Pharma degree from a recognized university.
Experience
- 03 to 10 years of experience in INJ pharmaceutical IPQA
- Hands-on experience with QA- IPQA
Skills & Competencies
- Solid understanding of GMP regulations, ISO standards, and industry best practices for pharmaceutical manufacturing.
📌 Walk in Interview @ Papaya Tree Hotel Indore- QA (Ahmedabad)
🏢 Intas
📍 Ahmedabad
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