we are looking for a line lead to oversee the quality assurance of the product during production for a rapidly growing pharmaceutical company in Long Island. There is enormous opportunity for growth, pay rate increases, and bonuses. If you are looking for an opportunity where you can make an immediate impact with a company that is growing by 20% year over year this is your opportunity! Please contact Dillon at 631-760-2096 or text 347-620-1469
- Verify all raw material kits being used for bulk processing. - Compare the physicochemical chemical characteristics and the organoleptic properties of the production lot to an approved standard. - Sample and Release bulk product. - Bring released samples to the QC Laboratory for micro-testing. - Verify that all equipment used, (pH Meter / Viscometer) are in proper working order and are up to date on calibration. - Routine GMP inspections of the compounding floor and equipment. - Write-up and sign for all addendums after reviewed by R&D. - Collect weekly samples of Deionized water for laboratory. - Work in conjunction with R&D to monitor highly supervised batches such as pilot and validation batches. - Review the compounding section of the batch record to verify that the compounders were compliant with procedures. Any discrepancies are resolved before the product is released.
The essential functions of this role include:
- working in a smoke free environment
- Quality Control
- GMP Knowledge
- Line Work
- Production line
- Record keeping
- viscosity testing
- batch records
- Years of experience: 1 year
- Experience level:Experienced
Working hours: 8 AM - 4:30 PM
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