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.
This is an 11-month contract and is a hybrid position Purpose Provide quality oversight and direction for the introduction of...
Apply For This JobPurpose Associate Quality Specialist supports day to day QA activities in the facility. Responsibilities Participate as functional expert in the...
Apply For This JobThis is an 11-month contract and is a fully onsite position. Purpose Responsible for generating and expediting review and approval...
Apply For This JobPurpose Responsible for ensuring that the process for the manufacture of drug product is in compliance with cGMP and the...
Apply For This JobThis is a 23-month initial contract with an excellent salary, bonus, and benefits. Purpose Your job, as Quality Systems Team...
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.