Quality Control Officer
- Category: Data Entry Jobs
- Location: Guwahati, Assam
- Job Type: Full Time / Part Time
- Salary: Estimated: $ 16K to 33K
- Published on: 2025/09/21
QC ROLE (QUALITY CONTROL ) PHARMACEUTICAL COMPANY – GUWAHATI LOCATION Information : Experience: 3-7 Years Location: Guwahati / Able to relocate Guwahati Education: B Pharma / BSC Chemistry / MSC Chemistry Industry Type: Pharmaceutical Functional Area: QC Salary : Best in industry Job Description: The Incumbent as a member of the Quality Control Team is responsible for sampling, analysis, Testing, line clearance, release, related documentation and other related Quality Control functions in respect of RM/PM/Finished goods/ in process /Validation and stability samples. Job Responsibilities : 1. To sample the Incoming RM/Packaging material. 2. To conduct analysis and testing of RM/PM/FG/actives and intermediates with the help of analytical instruments and techniques. 3. To calibrates/verifies analytical instruments/balances 4. To Trouble shots analytical instruments 5. To coordinates and follows up with engineering dept for timely availability of their services to attend breakdowns. Interruptions and scheduling of maintenance. 6. To inspect Packaging lines and issues Line clearances 7. To review and update raw material and packaging material specifications 8. To prepare testing specifications. +. To prepare, review and update working standards. 10. To maintain calibration records of instruments. 11. To prepare trend analysis of finished products. 12. To generates PR for the Consumables/glass wares /chemicals and other laboratory aids /spares required for the dept. To perform Chemical assays and standardizations of reagents. 14. To prepare SOPs, reviews for biannual review. Prepare Training outlines. 15. To maintain and control inventory of Reagents. Chemicals/glass wares. 16. To conduct stability studies of reagents. 17. Prepares analytical reports and certificates of analysis. 18. To investigate laboratory errors/LIRs 1+. To validate instruments, equipments, processes, analytical methods. 20. To prepare and evaluate stability data 21. To prepare stability protocols 22. To validates stability indicating methods Candidate Profile: Education: BSc Chemistry / Msc Chemistry , B pharm Experience: 3 to 7 years of experience in Quality Control Department of a solid dosage forms manufacturing pharmaceutical company. You Can share your resume at Adm17@cyno.co.in
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