Inspector; QA Manufacturing - 3rd Shift (11:00PM - 7:30AM)
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Summary
Third-shift (11:00PM–7:30AM) QA Manufacturing Inspector at Contract Pharmacal Corp who safeguards product quality across all manufacturing phases in line with cGMP — performing in-process checks (weight, hardness, friability), AQL sampling, room clearances, batch record release/review, and environmental monitoring support.
Position Summary:
The Inspector, QA Manufacturing has the primary responsibility of ensuring product quality is maintained through all phases of manufacturing in accordance with current good manufacturing practices.
Responsibilities: Responsibilities include, but are not limited to:
- Perform in-process monitoring (e.g. weight, thickness, hardness, disintegration, friability, etc.) of all manufacturing operations
- Perform duties using good documentation practices
- Collect in-process and finished product samples as required
- Support collection of microbiological samples per procedure as required
- Perform room inspections/clearances as required
- Perform Batch Record release of both Commercial and IP batch records
- Perform AQL sampling and inspections as required
- Identify and report any non-conformances/discrepancies to management if applicable
- Review general SOPs are being met by production
- Assist in employee training (initial and ongoing)
- Support environmental monitoring activities (i.e. water sampling air sampling)
- Provide additional QA technical support to Coating Department
- Review batch record documentation
- QMS form issuance as required to production
- Daily scale weight verification
- Maintain QA supplies
- Review and approve weekly pest control logs
- Sample transmittal to QC and Account Services
- Review grounds logbook for Maintenance
- Monthly audit of facility fire extinguishers
- Other responsibilities as assigned by Senior Management