Job description
We are currently looking to fill a Principal GMP Auditor position. This role is responsible for planning and conducting quality audits in manufacturing (GMP) within designated Quality Auditing area.
In this role, a typical day might include the following:
Scheduling, preparing, and conducting audits in support of GMP as advised
Assembling and coordinating the activities of the audit team
Performing audits in accordance with Regeneron standard operating procedures and quality policies• Raising any compliance issues
Communicating audit results to management and auditees through written audit reports
Leading post-audit activities, and following up on any vital corrective and preventive actions by resolving any issues
Assisting with hosting regulatory facility inspections by acting as a scribe and/or document reviewer
Drafting and issuing periodic reports to site management as requested
Assisting with training/orientation for new Quality Auditing staff
This role might be for you if you:
Are able to interpret policies, standards, and regulations, and then evaluate potentially critical problems not covered
Can ensure that we are following written procedures, and exercise judgment in evaluating quality systems, processes, procedures, and protocols for compliance
Have the ability to stand and walk for extended periods of time
Enjoy travel, domestic and international, 50% of your time
Have experience in aseptic CMO auditing
To be considered for this role you must hold a Bachelors degree with the following amount of experience in the Biotech/Pharmaceutical industry, audit experience in GMP environment preferred.
GMP Auditor: 2+ years
Sr GMP Auditor: 5+ years
Principal GMP Auditor: 8+ years
Other proven experience may be considered in lieu of degree. Level is determined based on qualifications relevant to the role.
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Salary Range (annually)
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