About the Role:
A reputed pharmaceutical manufacturing facility in Boisar (MIDC Boisar, Tarapur) is hiring an IPQA (In-Process Quality Assurance) Officer to ensure strict adherence to cGMP and regulatory standards during production.
Key Roles & Responsibilities:
• Conduct routine in-process quality assurance checks and line clearances across dispensing, manufacturing, compression, coating, and packaging stages.
• Review Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) concurrently for accuracy and regulatory compliance.
• Perform environmental monitoring, swab sampling, and collect intermediate/finished product samples for laboratory evaluation.
• Identify and report process deviations, out-of-specification (OOS) conditions, and participate in initial investigation exercises.
• Enforce cGMP compliance, data integrity, and hygiene protocols across the shop floor.
Candidate Profile & Requirements:
• Educational Qualification: Any Graduate / Relevant Experience.
• Experience: Freshers Allowed.
• Thorough familiarity with cGMP guidelines, pharmaceutical line clearance, and in-process sampling techniques.
• Strong attention to detail and good documentation practices (GDP).
• Working Schedule: Regular shift.
• Gender Preference: Male & Female.
• Location: Boisar (MIDC Boisar, Tarapur).
• Compensation: Depends on interview.
How to Apply:
Eligible and interested candidates are encouraged to apply directly through Jobrabit. Applications will be reviewed by Yukti Placement Services, and shortlisted candidates will be scheduled for interview screening in Boisar.
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