Job Overview
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Date PostedApril 29, 2023
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Location (State / UT)
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Expiration date--
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Experience2 Years, 5 Years
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GenderAny
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Desired QualificationMaster’s Degree
Job Description
Roles and Responsibilities
- Analysis of In-process, Intermediates, Raw material, Packing material, Finished products, Stability study, Hold time study, Process validation, Cleaning samples, Vendor development, and any analysis allocated by the team leader and release with proper documentation.
- Ensuring analysis is performed in compliance with GLP.
- Ensuring analysis raw data is documented on-line.
- Initiation, Completion, and filing of Daily analysis reports.
- Ensuring any abnormal results, incidents, deviations, and discrepancies are reported immediately to the reporting Section Head.
- Ensuring all relevant log entries are made for every activity wherever applicable.
- Supervise compliance to all cGMP, GxP, or any other regulatory requirements including EHS requirements.
- Report any quality concerns or suggestions for improvements to Department Head.
- Execute and supervise all tasks and activities as per the applicable SOPs and company policy.
- To maintain the safety norms while working in the lab. (e.g. Wear goggles, PPE, Disposal of sample/media as per procedure, etc).
- Ensuring analysis is performed as per valid procedures and by using calibrated instruments / Standards.
- Ensuring self-discipline with respect to wearing aprons, attendance, and personnel hygiene and interrelations.
- To perform Labware LIMS-related activities.
- Any other assignment was given by the Section Head or Department Head.
Desired Candidate Profile
- Qualification: B.Sc,/M.Sc
- Experience: 1-5 Years of all cGMP, GxP, or any other regulatory requirements
Interested Candidates can Apply with their most recent CTC Break-up