Role & responsibilities
Perform sampling and testing of Raw Materials (RM), Packaging Materials and Finished Products
Handle stability study samples, including sample withdrawal, testing, documentation and monitoring of stability schedules.
Perform/coordinate Finished Product analysis as per approved specifications and test methods.
Ensure proper sampling, labelling, handling and storage of RM and Finished Product samples.
Review analytical results, laboratory records, worksheets and related QC documentation.
Maintain stability chambers/sample storage areas and monitor temperature/humidity conditions as applicable.
Support OOS/OOT investigations, deviations, CAPA and laboratory investigations.
Preferred candidate profile
Qualification: B.Sc./M.Sc. in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry or equivalent.
Experience: 27 years of relevant experience in Pharmaceutical Quality Control.
Candidates having hands-on experience in Stability, Finished Product Analysis and Raw Material Sampling will be preferred.