We’re hiring!
Anthem
invites applications for Quality Assurance Auditor - GLP.
Responsibilities:
• Assure Test Facility Management, compliance to OECD Principles of GLP
and terms and conditions of National GLP Compliance Monitoring Authority with
respect to GLP functions.
• Conduct Study, Facility and Process Based Inspections and vendor
audits.
• Prepare Standard Operating Procedure(s) to describe procedures related
to Quality Assurance, Management SOPs as applicable in compliance with
principles of GLP.
• Review SOPs to support applicable regulatory requirements specific to
system compliance.
• Review Master Schedule for accuracy and completeness and facility
general documents like IQ, OQ & PQ
• Identify critical phases of a GLP study for in-process audit with the
Study Director.
• Issue QA statement to GLP study after Study Director has signed the GLP
Compliance Statement
Qualification: M.Sc (Biotechnology/Microbiology/Chemistry)/ M. Pharm/ Veterinary
Sciences with 2-4 years of industrial experience. The following skill set will
be an added advantage:
• Preclinical Toxicology studies
• Microbiology (AMES studies)
• Physico-Chemical Studies
• Analytical/bioanalytical studies
Applicants can send their resumes to careers.qa@anthembio.com
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