Walk in Interview @ Papaya Tree Hotel Indore- QA -IPQA Sterile

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

• Strong understanding of GMP regulations, ISO standards, and industry best practices for pharmaceutical manufacturing.