Quality Control Supervisor
2 weeks ago
The QC Supervisor reports to the Quality Manager. The primary responsibility of this position is to manage all aspects pertaining to Quality Control of all products packaged/produced at the facility.
Responsibilities:
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Accomplishes department objectives by managing staff; planning and evaluating department activities.
- Maintains staff by conducting interviews, selecting, orienting, and training employees.
- Accomplishes staff results by communicating job expectations, planning, monitoring, and appraising job results.
- Coaches, counsels, and disciplines employees
- Scale calibration program – review for completion, sign off and file
- Moisture meter calibration - review for completion, sign off and file
- Gluten program – ensures materials are being tested. Raw materials and finished goods. Results are reviewed, signed off and filed away appropriately.
- Raw material sampling and retention program – oversee entire program. Ensure samples are catalogued correctly and all associated documentation is complete.
- ATP and allergen swabs – train employees, review forms for completion, sign off and file
- X Ray verification program- review for completion, sign off and file
- QC Testing results review, sign off and file
- QC line check review, sign off, and file
- Blending documentation – review for completion, sign off and file
- Allergen program – be able to be a key figure in ensuring compliance with allergen labeling, stacking, cleaning etc. in the warehouse and production areas.
- Conduct GMP inspections per JJM’s program
- Assist Chemical control program- ensure documentation is complete, conduct chemical control audits per JJM’s program
- Assist Glass and brittle plastics program – ensure documentation is complete, conduct the audit per JJM’s program
- Reviewing and approving staff hours, ensuring appropriate coverage for call outs, weekend coverage, etc.
- Be the liaison for the floor techs to answer questions regarding packaging issues, etc.
- Review and release of pre-ship materials, incoming ingredients, bulk finished materials and packaging – organoleptic, other testing, COA/COC review
- Utilize and understand Plex (ERP) in review and release
- Employee training (QC) and follow up evaluation
- Attend production meetings
- Audit support
Requirements:
High School Diploma or GED
Minimum 5 years of experience with Quality Control in Pharma, Food, or Dietary Supplements
Minimum 5 years is a supervisory role
Knowledge of GMP’s, HACCP, HARPC, & Food Safety
Bilingual (Spanish) required
Experience with ERP Systems
Must have attention to detail
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