Description
A QA Specialist is required for a 7 month contract with a global biotech company near Dublin.Role and responsibility:
* Plan and perform routine analyses with efficiency and accuracy.
* Plan and perform multiple, complex routine/non-routine methods and procedures.
* Report, evaluate, back-up/archive, trend and approve analytical data.
* Troubleshoot, solve problems and communicate with stakeholders.
* Initiate and/or implement changes in controlled documents.
* Participate in audits, initiatives, and projects that may be departmental or organisational in scope.
* Introduce new techniques to QA Incoming, including method transfers, reports, validations and protocols.
* Evaluate lab practices for compliance and operational excellence improvement on a continuous basis.
Requirements:
* Take initiative to identify and drive improvements
* Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls)
* Escalate issues professionally and on a timely basic
* Applies research, information gathering, analytical, and interpretation skills to problems of diverse scope
* Interprets generally defined practices and methods
* Able to use statistical analysis tools to perform data trending and evaluation
If this is you please apply today.