VERVE Human Care Laboratories (A Unit of Venor Pharma Ltd.) is hiring for Lab QA (Quality Assurance) Details are Provided below 1. Position: Lab QA (Quality Assurance) 2. Experience 3 to 8 Years 3. No. of Positions 2 4. Qualification: M.Sc / M. Pharma 5. Key Responsibilities: -Review and approval of laboratory documents (SOPs, Methods, Specifications, Reports, etc.) -Ensure compliance with cGMP, GLP and regulatory requirements -Handling change control, deviation, CAPA and OOS/OOT investigations -Review of analytical data and batch records -Support during internal and external audits -Ensure data integrity and documentation compliance -Grow Learn Make an Impact in a Regulated Pharma Environment -Quality People Build a Healthier Tomorrow 6. Work Location: Plot No. 15A, Pharmacity, Selaqui, Dehradun, Uttarakhand 7. How to Apply : Share your updated CV at hr.manager@vervehumancare.com Click Here For Details Click Here For Web...
MULTIPLE VACANCIES AT DRUG SUBSTANCE PRODUCTION ( USP, DSP, QMS ) , QUALITY ASSURANCE (IPQA, QMS ) , QUALITY CONTROL ( PROTEIN LAB , BIOASSAYS , RMPM) - M. SC./ B. TECH. / B. E. / M. TECH. IN BIOTECHNOLOGY
MULTIPLE VACANCIES AT ZYDUS BIOLOGICS WALK-IN INTERVIEW FOR ZYDUS LIFESCIENCES LIMITED, PUNE Hiring for Zydus Biologics, Ahmedabad 1. Drug Substance Production a. USP Production: i. Experience in the fermentation department with a minimum of 2 years of experience of working in mammalian culture. ii. The person should have handled SS bioreactor / fermenter having a capacity of 500 L or more. b. DSP Production: i. Experience in the purification department with a minimum of 2 years of experience in working on mammalian culture products. ii. The person should have handled the chromatography system (capacity: Minimum 600-L/h or more). Column (Capacity: 600 mm or more diameter), and Automated TFF system. c. QMS Production: i. Risk assessment, Root cause analysis for deviations, OOT, OOS, and QMS document via Trackwise. ii. Reviewing cGMP and equipment qualification. 2. Quality Assurance a. IPQA: i. Hands on experience in QA Oversight...