Senior QC Associate

QC Associate is required to join a global biotech company, located near Dublin. The QC specialist will be required to manage all sample management activities throughout the site, create/own and approve protocols, sample plans, SOP and documentation and have site ownership of stability programme.

Role and responsibilities:
. Responsible for SAP and LIMS functions/transactions within the sample management remit
. Site ownership of Reference standards and reserves
. Out of hours responder for sample management equipment (fridges/freezers/incubators)
. Responsible for their own training and safety compliance.
. Sample shippments and temperature monitoring activities.
. Under minimal supervision, be responsible for one or more of the following activities in QC, including sample and data management and equipment maintenance.
. Contribute to team by ensuring the quality of the tasks/services provided by self
. Contribute to the completion of milestones associated with specific projects or activities within team

Relevant experience:
. Bachelor's degree in a Science-related field is required.
. 5+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.

If this is you please apply today