This is an 11-month initial contract.
Responsible for ensuring that the process for the manufacture of drug products at our Carlow site 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, and consistent with Company 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 the interview, as patterns of shift will differ at project stages/s.
Responsibilities Provide Quality support to IPT production teams to ensure cGMP standards are maintained. Understanding of sterile manufacturing operations is...
Apply For This JobThis is an 11-month initial contract. Purpose: The Specialist is a member of a team within Quality and is involved...
Apply For This JobThis is a 12-month initial contact. Purpose The Senior Quality Audit Specialist will be responsible for supporting the Alexion audit...
Apply For This JobPurpose The Quality Systems Specialist is responsible for maintaining and continuous improvement of the Quality Management System throughout their knowledge...
Apply For This JobThis is an 8-month contractor position. Hybrid position – 3 days onsite, 2 days remote. Purpose This role serves as...
Apply For This JobThis is a 12 month contract. Purpose The Medical Device QA Specialist is to provide QMS support for combination products...
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.