4 Job openings found

1 Opening(s)
15.0 Year(s) To 25.0 Year(s)
17.00 LPA TO 25.00 LPA
Providing technical assistance to the Facility design team in the drawings for Sterile API both Crystalline and Lyophilization facilities.  Providing technical assistance to the Project Management system (PMS) team in the finalization of required equipment with make, model, capacity and placement in facility based up on the process flow for ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
12.00 LPA TO 14.00 LPA
A "QC Manager - Sterile Formulation" job description entails overseeing all quality control operations within a sterile injectable drug manufacturing facility, ensuring that all products meet stringent regulatory standards by managing testing procedures for raw materials, in-process samples, and finished products, while maintaining compliance with cGMP guidelines and conducting thorough ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
Overseeing Microbiology operations for both Oral Solid Dosage (OSD) and Liquid Injectable facilities. Granting approval for microbiological test reports encompassing MLT, Environment, Water, Raw Materials (RM), Finished Products, Sterility, BET, Calibration, and Analytical Method Validations. Providing assistance to the Research and Development (R&D) team in microbial method development. Collaborating with other departments to ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 18.00 LPA
Experience in Business Development / Sales / Marketing / In licensing / Out licensing of pharmaceutical formulations (ideally Injectable & Sterile) with a minimum of 10+ years . Must have worked in similar role with a reputed pharma company. Build contacts with potential clients to create new business opportunities Keep prospective client ...

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