Responsible for ensuring that the process for the manufacture of drug product is in compliance with cGMP and the associated regulatory requirements. Responsible for reviewing and approving GMP documentation to support corporate compliance/regulatory expectations for manufacturing operations. Ensure that objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers.
For Applicants, it is important to note that this will be a Shift IPT Role. The Shift pattern will be discussed in interview, as patterns of shift will differ at project stages/s.
Documentation:
Quality Oversight:
Continuous Improvement:
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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.