Job Overview
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Date PostedOctober 22, 2023
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Location (State / UT)
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Expiration dateSeptember 12, 2024
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Experience3 Years, 6 Years
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GenderMale
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Desired QualificationMaster’s Degree
Job Description
Roles and Responsibilities:
- Responsible for analysis of finished products, stability samples, and packing material in the Quality control department.
- Responsible for document preparation required in Laboratory (ARS, MOA, Specification, Reports stability study protocol, and SOPs.
- Responsible for review of documents and daily activity roles in the QC laboratory.
- Responsible for maintaining the ALCOA in the QC laboratory.
- Responsible for the Preparation of reagents and chemicals, and volumetric solution preparation.
- Responsible for testing review & and release of packing material, Stability product analysis whenever applicable.
- Responsible for Maintaining records of Working standards/ Primary standards and Reference standards.
Desired Candidate Profile:
- Qualification: M.sc. (Chemistry)/ B.Pharma
- Candidates from the Pharmaceutical industry (Formulation/ API) will be preferred.
Perks and benefits:
1. Transport facility
2. Canteen facility