This is an 11-month contract and is a fully onsite position.
Responsible for generating and expediting review and approval processes for QC GMP documentation including but not limited to Quality Notifications, Laboratory Investigations, CAPAs, Effectiveness Checks, Standard Operating Procedures, Standard Work Instructions and change controls, Annual Product Reviews, Trend Reports, Out of Process Control Limit events, Compendial Assessments. Author/ Provide technical expertise and technical oversight of the above QC documentation. Ensure that objectives are effectively achieved, consistent with Company requirements to ensure compliance, safety, and reliable supply to our customers.)
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Apply For This JobTo apply for this job email your details to rachael.kennedy@theaphexgroup.com.
To apply for this job email your details to rachael.kennedy@theaphexgroup.com.