Sr Associate QC is required for a South Dublin based Biopharmaceutical company that specialises in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
The Senior Associate QC will be responsible for:
o With a high degree of technical flexibility, work across diverse areas within the lab
o Plan and perform routine analyses with efficiency and accuracy.
o Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
o Report, evaluate, back-up/archive, trend and approve analytical data.
o Troubleshoot, solve problems and communicate with stakeholders.
o Initiate and/or implement changes in controlled documents.
o Participate in audits, initiatives, and projects that may be departmental or organizational in scope.
o Write protocols and perform assay validation and equipment qualification/ verification.
o Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
o Evaluate lab practices for compliance and operational excellence improvement on a continuous basis.
The Sr Associate QC will require:
o Bachelor’s degree in a science discipline.
o 3+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
o Experience with regulatory compliance in GMP manufacturing and testing of pharmaceutical products.
Call Conor in LSC on 0214777 329 to discuss this Sr Associate QC role in more detail or apply directly via this advert.