ASSISTANT MANAGER

Biocon · Remote

Source and collection record

Last observed by our collector: 8 October 2026 at 11:11 pm IST. This is not a manual review or a confirmation from the employer.

Employer requisition: 20057

Job type and experience labels are automated discovery categories. The employer determines eligibility. Original experience wording was not retained separately; check the current employer page.

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Collected role description

Role Summary: 1. Master degree in any Chemistry / Biochemistry / Biotechnology/Life science. 2. Basic knowledge in chemistry and Biology. 3. Good Knowledge on handling of LIMS software in Quality control (LIMS template creation, Sample Management Lot / Batch creation, Stability Management, Review and Approval Process in LIMS etc...) 4. Knowledge on chromatography techniques (HPLC and GC) and other pharmaceutical Instruments. 5. Trouble shooting of existing analytical methods and highly skilled in chromatography techniques. 6. Knowledge on preparation of SPEC and Standard testing procedure. Review of Dossier, TTD and JOS. 7. To handle QMS documents like Deviation, OOS, Change control, CAPA and Lab Incidents. 8. Raising, tracking, investigating and closing QMS elements (Change control, Deviation, OOS and Lab Incidents). 9. Planning and designing of experiments, preparation of SOP's and Specifications. 10. Trending of historical data. 11. Knowledge on cGMP and GLP practices. 12. Ready to work in a team and shifts. 13. Ready to accept responsibilities. 14. To have good team coordination and cooperation. Key Responsibilities: 1. Master degree in any Chemistry / Biochemistry / Biotechnology/Life science. 2. Basic knowledge in chemistry and Biology. 3. Good Knowledge on handling of LIMS software in Quality control (LIMS template creation, Sample Management Lot / Batch creation, Stability Management, Review and Approval Process in LIMS etc...) 4. Knowledge on chromatography techniques (HPLC and GC) and other pharmaceutical Instruments. 5. Trouble shooting of existing analytical methods and highly skilled in chromatography techniques. 6. Knowledge on preparation of SPEC and Standard testing procedure. Review of Dossier, TTD and JOS. 7. To handle QMS documents like Deviation, OOS, Change control, CAPA and Lab Incidents. 8. Raising, tracking, investigating and closing QMS elements (Change control, Deviation, OOS and Lab Incidents). 9. Planning and designing of experiments, preparation of SOP's and Specifications. 10. Trending of historical data. 11. Knowledge on cGMP and GLP practices. 12. Ready to work in a team and shifts. 13. Ready to accept responsibilities. 14. To have good team coordination and cooperation.