Job Overview
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Date PostedDecember 9, 2022
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Location (State / UT)
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Expiration date--
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Experience3 Years, 8 Years
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GenderAny
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Desired QualificationBachelor Degree, Master’s Degree
Job Description
- Responsible for all Production activities with respect to cGMP.
- Responsible for shift operations being a shift incharge.
- Sound knowledge of documentation exposure of cGMP.
- Completion of BPCR, Equipment Log Book/ Shift & all cGMP Records.
- Monitoring the shift activities for both Quality & Quantity aspects.
- Co-Ordinating with warehouse, QA, QC & Engg. Department, to run the shift activity (Smoothly) without any hiccups.
- Maintaining proper documentation of the batch manufacturing records requisitions in process.
- Maintaining good housekeeping on the shop floor. .
- Maintaining the safety on shop floor and giving training on safety for shop floor people.
- Controlling the manpower & achieving the production target as per schedule by following proper Quality & Quantities control.
- To improve Plant environmental conditions as per SHE regulations.
Qualification: B.Tech/B.E. in Bio-Chemistry/Bio-Technology, Chemical, MS/M.Sc(Science) in Biotechnology, Organic Chemistry, Chemistry