QA Officer in PAR Laboratories for B.Pharm, M.Pharm In Gujarat
• Review of Batch Manufacturing Record.
• Review of Batch Packing Record.
• Preparation of Standard operating procedure of QA.
• Issuance of BMR and BPR.
• Batch release.
• IPQA activity.
• Line - clearance in granulation ,compression , Packing.
• Preparation of APQR.
• Review Analytic work report.
• Preparation of process validation protocol and reports.
• Preparation of preventive maintenance schedule.
• Monthly check of Temperature and Humidity record and log-books.
• Any other responsibly given by higher management.
Experience: 1-3 year
Qualification: B. Pharm./M.Pharm./M.Sc.
Location: Gozaria, Gujarat
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: QA
End Date: 17th Oct, 2013
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As
a dedicated manufacturer and marketer of Hormone products, the Company
concentrated on the niche areas of operations. With its beginnings in
Mumbai, PAR Laboratories has been providing quality hormones and
contraceptive products to various markets around the world.
Post
QA Officer - 2
Job Description
• Review of Batch Manufacturing Record.
• Review of Batch Packing Record.
• Preparation of Standard operating procedure of QA.
• Issuance of BMR and BPR.
• Batch release.
• IPQA activity.
• Line - clearance in granulation ,compression , Packing.
• Preparation of APQR.
• Review Analytic work report.
• Preparation of process validation protocol and reports.
• Preparation of preventive maintenance schedule.
• Monthly check of Temperature and Humidity record and log-books.
• Any other responsibly given by higher management.
Additional Information
Experience: 1-3 year
Qualification: B. Pharm./M.Pharm./M.Sc.
Location: Gozaria, Gujarat
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: QA
End Date: 17th Oct, 2013
where to forward CV - hr.parlabs@gmail.com
For more Jobs visit Jobes Mantra
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