Description
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