What are the responsibilities and job description for the Pharmaceutical Laboratory Manager position at Glenmark Pharmaceuticals USA?
Job Responsibilities
As a member of our Quality Control team, you will be responsible for ensuring compliance with cGMP standards and maintaining data integrity in the QC lab. You will work closely with the QC Manager to achieve these goals.
Key Responsibilities
- Perform quality control analysis in compliance with cGMP standards prescribed by USFDA.
- Maintain data integrity and compliance in the QC lab according to USFDA standards.
- Perform instrument qualification and calibration in the QC lab under the guidance of CQA.
- Execute procedures and systems for raw materials, packaging materials, finished products, and in-process testing in the QC lab.
- Provide information and data for stability study evaluation and execution according to quality and regulatory requirements.
- Complete testing on time and ensure compliance during analytical TT and AMV performed in the QC lab.
Education and Experience
- Bachelor's degree in Chemistry or Pharmaceutical Sciences.
- 4 years of experience in pharmaceutical manufacturing facilities, preferably in Quality Control.
- Background in Stability, Finished Goods, and Raw Materials with some experience in Analytical R&D.
