Packaging

Openings in R&D, AR&D, Production, Labelling & Packing at Hetero Biopharma. Process development & scale-up. Tech transfer experience. DoE / QbD based process studies

Media Preparation and GPT, Microbiological Limit Test and assay, Water analysis, Environment Monitoring, Culture Handling, Personal Hygiene Monitoring

Operate & manage granulation, compression, coating, pelletization and capsule filling area. Operate and monitor pharmaceutical manufacturing equipment as per SOPs, BMRs, and GMP guidelines.

Compression, Coating, Granulation & Blending. Maintaining BMR of Solid dosage form and related logbooks during process, production activities in line with cGMP norms and applicable SOPs.

Handling of Change Controls, CAPA's, Unplanned Deviations, Planned Deviation, Investigations and Audit Management in Trackwise software

Sun is building the future of healthcare. We invite passionate professionals to join India's No. 1 pharmaceutical company and help deliver medicines that change lives worldwide.

IPQA, Vendor Qualification, Technology Transfer, QMS, Validation, Qualification, Documentation Quality Risk Assessment

Candidate should have handled KF, Potentiometer, GC, HPLC and IC instruments. Candidate should have exposure to the analysis of Raw material. API & Excipient. Should have exposure for testing of Stability, FP samples.

Monitor and supervise production process to ensure compliance with SOP and cGMP. Maintain documentation as per regulatory authorities requirement like change control, deviations.