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 (India)
🏢 Intas
📍 India
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