Company Jobs

Handle Product Quality Complaints, Root Cause Analysis and CAPA. Manage Change Control, Deviations, OOS/OOT and Compliance Activities

Bachelos or Masters degree in Life Sciences, Chemistry, Biotechnology, Pharmacy, or a related field.

Candidate must have extensive experience in pharmaceutical production operations with strong knowledge of CMP, team handling, production planning, documentation, and coordination with QA / QC.

Candidate must have strong hands-on experience in QMS activities including Deviation, CAPA Change Contol, OOS handling. SOP documentation, and regulatory audit support in injectable / parenteral manufacturing.

Regulatory exposure in a sterile pharmaceutical manufacturing environment is mandatory.

Control manufacturing activities in the respective section to ensure activities carried out are as per requirement of cGMP & safety to meet the quality and manufacturing targets in time

Exposure of analysis for Finished Products, Stability Samples & Raw Materials. Having Knowledge of Analytical Method Validation, Verification & Method Transfer. Having skill for data interpretation, troubleshooting. Pharma knowledge of Solid orals & Quality process.

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

Monitor the production activities in a shift by maintaining cGMP and safety norms to achieve production targets