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Covalent Laboratories Private Limited is a USFDA, EU-GMP & ISO 14001(2004) Certified & reputed pharmaceutical company, pioneering and leading in Cephalosporin products since 2003 in the global and domestic market. The role of Production Supervisor involves supervising API manufacturing steps, ensuring adherence to BMR, and coordinating with maintenance and quality teams.
Role requires 2–10 years of pharma or formulation plant experience, with involvement in charging, sampling, filtration,
rated by Project and Maintenance Executive in Hyderabad
Assist in API manufacturing processes as per Batch Manufacturing Records (BMR).
Support charging, sampling, filtration, centrifugation, drying, and packing activities.
Monitor process parameters and report deviations to supervisors.
Role Category: Production & Manufacturing - Other
Education
UG: Any Graduate
Key Skills
Skills highlighted with ‘‘ are preferred keyskills
Covalent Laboratories Private Limited is an USFDA,EU-GMP & ISO 14001(2004) Certified & Reputed Pharmaceutical Company, pioneer & Leader of producing Cephalosporin products since 2003 in theGlobal/Domestic market.