Job Description: Accountabilities/Responsibilities: 1. To perform analysis and review of analytical data for routine samples (In-process samples, Drug substances, Drug product release and stability samples), method transfer and method validation. 2. Preparation and review of Documents (Specification, STPs, TDS, SOP, COA, MVP, MVR MTR etc.) 3. Coordination with vendor for external calibration and with QC personal for in-house calibration and verification of laboratory instruments and equipment. 4. QC materials (Chemicals, standards, kits and consumables) indent. 5. Maintenance and management of laboratory equipment and instruments. 6. Analyst qualification and QC employees training 7. Initiation, investigation and tracking of QMS activities 8. Ensure QC lab compliance in accordance with cGMP Educational qualification: M.SC., M. Pharm or Master degree in Biotech or relevant subjects Experience: 3-7 years of experience in tasks such CEX-HPLC, SE-HPLC, ELISA and Capillary. Electrophoresis analysis. Soft skill competencies: Well versed with computer skill MS word, PPT etc
Employement Category:
Employement Type: Full time Industry: Pharma / Biotech Role Category: Front Office / Receptionist Functional Area: Not Applicable Role/Responsibilies: Senior Executive/ Executive for Method