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Exposure to aseptic process activities, aseptic techniques, aseptic filling and sealing activities, and media filling activities. Experience in operating autoclaves and terminal sterilizers. Preparation of autoclave loads, loading and unloading of autoclaves and sterilizers

The ideal candidate will be responsible for compiling Drug Master Files DMFs and Certificates of Suitability CEPs, ensuring compliance with global market regulations and emerging market standards in accordance with ICF guidelines. This role requires strong coordination with internal stakeholders and expertise in regulatory submissions, amendments, and annual reports.

M.Pharm / MSc; Experience in Analytical Method Development of Assay, Related Substances and Dissolution method for oral solid dosage form. relevant experience with OSD products for Regulatory Market in the Analytical Department.

B.Pharmacy / M.Pharmacy; Candidate should have Injectable experience and sound knowledge on manufacturing and packing activities of liquid and Lyo products. Aseptic process simulation, process validation, cleaning validation, Batch records review and batch release.

Bachelor of Pharmacy; Exposure in Pellets, Hard Gelatin Capsules, Soft Gelatin Capsules & Packing in OSD Formulation Manufacturing. Exposure in Pellets, Hard Gelatin Capsules, Soft Gelatin Capsules, Tablet & Packing

Execute the production planning in Liquid manufacturing block and ensure the production plan achievement as per plan. Responsible to ensure the entry and exit, gowning and personnel hygiene procedures are followed in liquid manufacturing block.

Seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other groups. Master degree in pharmacy/ life science/Biology/Biotechnology/ Biochemistry/Diploma in Clinical Research

B.Sc/M.Sc/ B. Pharm/ M.Pharm with relevant experience. HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC/ GLP; Hetero Drugs is an Indian pharmaceutical company and the worlds largest producer of anti-retroviral drugs. Heteros business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.

B.Sc / M.Sc / B.Pharma / M.Pharma; Review HPLC methods, chromatograms, and system suitability. Ensure HPLC sequences comply with methods. Prepare and review IQ, OQ, and PQ for new instruments. Conduct pre-investigations for OOS, OOC, OOT, and lab incidents. To perform line clearance, FG Sample withdrawal, Online GMP Monitoring, To Support of Product and Process Validation