QC Officers / Executive

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.