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GUARDIAN DRUG COMPANY, INC. Chemist in Dayton, New Jersey

Chemist, Dayton, NJ: Handle technical operations of Solid, Liquid and Dry Powder dosage forms. Involve in different processes of Solid Drug Dosage production development cycle like; Dispensing Raw materials, Sifting, Granulating, Blending, Milling, Tablet compression, looking after troubleshooting, stage wise yield calculation, label and weigh finished products as per Sop’s. Monitor production activities per cGMP compliance. Prepare process validation protocols and SOP per cGMP guidelines. Coordinate activities of manufacturing team in a Unionized environment. Coordinate with materials management and QA documentation to ensure scheduling efficiency and batch record completion. Maintain various production batch record (PBR), reconciliation records, in-process check records. Revise and update batch records, SOP’s & validation protocols as required. Ensure that manufacturing operations were performed in compliance with batch records, SOP’s and cGMP’s. Support R&D in process development and optimization of new products. Conduct cGMP training to operators. MS (BS + 5yrs exp) in Pharmacy, Chemistry, or related with two years’ experience. Mail resumes to Guardian Drug Company, 2 Charles Court, Dayton, NJ 08810 or email hr@guardiandrug.com. Refer FMC2025-JPP

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