Lead Chemist, Dayton, NJ:
Handle tech ops of Solid, Liquid & Dry Powder dosage forms. Involve in processes of Solid Drug Dosage production development cycle like; Dispensing Raw materials, Sifting, Granulating, Blending, Milling, Tablet compression, troubleshooting, stage wise yield calculation, label & weigh finished products as per SOP’s. Monitor production activities per cGMP compliance. Prepare process validation protocols & SOP per cGMP guidelines. Coordinate activities of manufacturing team in a Unionized environment. Coordinate with materials management & QA documentation to ensure scheduling efficiency & batch record completion. Maintain various PBR, reconciliation records, in-process check records. Revise & update batch records, SOP’s & validation protocols as required. Ensure that manufacturing operations were performed in compliance with batch records, SOP’s & cGMP’s. Support R&D in process development & optimization of new products. Conduct cGMP training to operators. MS (BS + 5yrs exp) in Pharmacy, Chemistry, or related W/2 yrs exp. Mail resumes to Guardian Drug Company, 2 Charles Court, Dayton, NJ 08810 & ref NV1010.