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. In July 2015 the site opened a $300million investment, which added significantly to the sites laboratory, filling, packaging and distribution (including cold chain) capabilities. The site is a fast paced, collaborative, team based working environment, where you get an opportunity to work with other highly skilled staff in a strategically important site in the companies global supply chain.
The Sr Associate QC will:
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.
The Sr Associate QC will require:
o 3rd level degree in a relevant discipline
o At least 3 years solid GMP pharma experience
o 4 years extensive HPLC experience with Empower software
o Peer to peer review experience
o Experience and comfortable with general GMP IS systems, electric lab notebook, QMTS, LIMS.
Call Amparo in LSC on 0214777 329 to discuss this Sr Associate QC role in more detail or apply directly via this advert.