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.

📌 QC Officers / Executive (Mehsana)
🏢 Lincoln pharmaceuticals
📍 Mehsana