Qualification & Experience : Ph.D/M.Sc in Biotech/ Biochemistry/ Microbiology/ Chemistry/ Life Science with 12 to 20 years of relevant experience in sterile and Vaccine formulations/ Bulk Antigens (Biologicals)
Job Description :
To lead & be responsible for Overall QC department activities including bench operations & Implementation of QMS as per WHO cGMP and GLP norms.
To lead the entire quality control team at the site and ensuring authorization of written procedures.
Ensuring process validation, Analytical method validations and calibration of analytical equipment.
To undertake all preparations and lead the team of QC for WHO and other regulatory audits, risk mitigation & automation.
OR
Attend the Walk in drive at Mohali & New Delhi on 9th and 10th Dec. For more details login to our website www.panaceabiotec.com
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