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Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector

Handling QMS as per Regulatory requirements. Handling Deviations, CAPA, Change Controls, OOS investigations. Responsible to process internal quality audits.

Strong understanding of formulation analytical method development. Working knowledge of ICH guidelines, SAP. and documentation systems.

Responsible for development, optimization, and scale-up of tablet formulations, ensuring product quality, stability, and regulatory compliance.

Should have hands on experience in Water samples analysis, In-process Bioburden and BET analysis, MLT analysis of Raw material and Packing material, Antibiotic assay by Microbial method and Sterility testing.

Akums Plant 1 specializes in the production of Oral Solid Dosage Forms, including tablets and capsules.

MSc / MPharm in Chemistry, Analytical Chemistry. Pharmaceutical Analysis or related field. 1 - 4 years of relevant experience in Analytical Development

Exposure to Manufacturing operations like Granulation, Compression, Coating, Capsule filling eBMR/ eBPR/ eLog/ Sap/QMS/trims and handling of SCADA

Communicate effectively with Elanco contacts from affiliate offices, call center contacts, legal, customer response teams, and other customer groups