ive- IPQA
2 weeks ago
Role & responsibilities
- Responsible for monitoring of basic norms of cGMP, ALCOA+ Principle, data integrity,
GDP & to maintain his personal health hygiene.
To handle IPQA team, assign shift of IPQA and monitor routine IPQA activities.
Need base, carried out the line clearance activity, In-process checks and Sample
collection at different stages of processing.
- To take round at Stores, Manufacturing, Primary Packing, Secondary Packing, BSR,
Scrap Yard and other areas.
- To Review BMR/BPR request and Material requisition and approve or reject request in
SCM for stores, Packing, Production and BSR.
- To approve Packing slip, MRN, Bar-coding, batch approval in Propix software and to
Verify Carton in Bar code Verifier.
- To review filled BPR and BMR before submitting to QA - documentation for batch release
and prepare Product Release Note for batch release and make trending of Observation
of Batch Card.
- To raise observation towards departments for any non - Compliance found during QA
review.
- To maintain destruction record of leftover samples, Validation samples and hold time
study samples.
To prepare, review and control of the standard operating procedures (SOP).
To prepare, review and control of Protocol and reports.
Preferred candidate profile
Candidate with 5-8 years of experience in formulation plant will be given preference here. Relevant candidate can share their profile on