QC Officers / Executive

Lincoln Pharmaceuticals Ltd.; Mahesana, Ahmedabad District; Vor Ort; INR 400.000 - 640.000; Vollzeit

Zusammenfassung

Lincoln Pharmaceuticals Ltd. is seeking a Quality Control Analyst in Gujarat to perform sampling and testing of raw materials, packaging materials, and finished products. The role includes handling stability samples, statistical monitoring of schedules, and coordinating product analysis as per approved methods.

The candidate should have hands-on experience in stability, finished product analysis and RM sampling, with a strong focus on laboratory documentation and QC processes.

Qualifikationen

• Hands-on experience in Stability testing and Finished Product analysis.
• Experience with Raw Material sampling and attention to QC documentation.
• Strong understanding of analytical methods and lab practices.

Aufgaben

• Perform sampling and testing of RM, packaging materials and finished products.
• Handle stability study samples, including withdrawal, testing, documentation and monitoring schedules.
• Perform/coordinate Finished Product analysis as per approved specs and test methods.
• Ensure proper sampling, labeling, handling and storage of RM and finished product samples.
• Review analytical results, laboratory records and QC documentation.
• Maintain stability chambers and monitor temperature/humidity conditions.
• Support OOS/OOT investigations, deviations, CAPA and lab investigations.

Kenntnisse

Stability testing

Finished product analysis

Raw material sampling

Ausbildung

BSc/ MSc in Chemistry or Analytical/ Pharmaceutical Chemistry

Jobbeschreibung

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.