Executive / Sr. Executive – Production (Peptides)

Department: Production Location: Ambernath Reports To: Manager – Production Education: B.Sc / M.Sc Chemistry / B.Pharm / M.Pharm / Chemical Engineering Experience: 4–8 years in pharmaceutical / API / peptide / chemical manufacturing industry About PolyPeptide Group PolyPeptide Group AG and its consolidated subsidiaries (“PolyPeptide”) is a specialized Contract Development & Manufacturing Organization (CDMO) for peptide- and oligonucleotide-based active pharmaceutical ingredients. By supporting its customers mainly in pharma and biotech, it contributes to the health of millions of patients across the world. PolyPeptide serves a fast-growing market, offering products and services from pre-clinical to commercial stages. Its broad portfolio reflects the opportunities in drug therapies across areas and with a large exposure to metabolic diseases, including GLP-1. Dating back to 1952, PolyPeptide today runs a global network of six GMP-certified facilities in Europe, the U.S. and India. PolyPeptide’s shares (SIX: PPGN) are listed on SIX Swiss Exchange. Purpose of the Role To lead and manage production activities while ensuring compliance with GMP standards, operational excellence, investigation management, and continuous process improvement in peptide manufacturing operations. Job Description for Executive / Sr. Executive – Production • Execute production activities as per production plan and targets while ensuring compliance with GMP norms and SOPs. • Perform manufacturing operations as per Master Batch Production Records. • Operate and manage equipment including Glass Reactors, Vacuum Tray Dryer, Prep HPLC, Rotary Evaporator, Nano Filtration, and Tray Lyophilizer. • Perform root cause analysis for manufacturing-related events and implement corrective and preventive actions (CAPA). • Ensure timely initiation and closure of quality events including Deviations, Incidents, Change Controls, OOS, and OOT. • Perform process risk assessments and support continuous improvement initiatives. • Prepare User Requirement Specifications (URS) for manufacturing equipment. • Prepare and review validation documentation including IQ, OQ, and PQ protocols. • Ensure compliance with quality systems and regulatory requirements. • Proficient in MS Word, Excel, and PowerPoint. Why Join Us at PolyPeptide Group PolyPeptide Group offers an exciting opportunity to work at the forefront of peptide-based therapeutics, a rapidly growing and innovative segment of the pharmaceutical industry. Join us and be part of a global organization shaping the future of life-saving therapies.