Address
Form of work- To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.
- QA overview for clean room behavior and aseptic activity.
- Review of batch processing records.
- Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release.
- Review of documents of respective areas and logbooks for adequacy and completeness.
- QA overview for receipt of material from warehouse to production.
- IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities.
- Review and Control of SOP’s, Specification, BPR issuance, Master Formulae and Records.
- Preparation & Review of process validation protocols and reports.
- Executing the validation/revalidation activity in the absence of authorized person.
- Any job activity assigned by HOD
- Responsible for regulatory audits with exposure equivalent to WHO Geneva PQ/USFDA
Job Types: Full-time, Permanent
Salary: Up to ₹30,054.61 per month
Schedule:
- Day shift
Application Question(s):
- Do yo have prior experience in Pharma Industry?
Work Location: In person
Speak with the employer
+91 8053449191
