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Required for Lab QA (Quality Assurance)- 02 Positions-M.Sc / M. Pharma

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...
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Jubilant Generics Limited requires Executive/officer

Jubilant Generics Limited are looking for a dynamic candidate to join 

Company: Jubilant Generics Limited, Roorkee

Position: Executive/officer - MSTG Technology Transfer
Experiences: 3 to 8 years
Qualification: B. Pharm/M. Pharm
Location: Roorkee (Uttarakhand)
Job Description:
  • Responsible for preparation of PPQ protocol/report/Scale up protocol/report
  • Responsible for preparation of qualitative and quantitative risk assessment for change in batch size/equipment etc.
  • Responsible for preparation of stability protocol
  • Responsible for preparation of Hold time study protocol and its Summary Report.
  • Tracking the outcome of CAPA of Deviation/OOS/OOT and completed within predefined time in CAPA Track wise.
  • Responsible for preparation of batch record
  • Responsible for continuous improvements in the commercial products at site to improve the efficiency, productivity, delivery and safety resulting in effective and efficient operation.
  • Handing of QMS documents such as deviation/ OOS/OOT/ Investigation/Market complaints.
  • Initiate the CCR accord to production plan.
Interested candidates can share their resume at varnika.chaudhary@jubl.com
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