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 ...