QC VALIDATION SPECIALIST required by CareerWise Recruitment for our Biotech client in Limerick.

The QC VALIDATION SPECIALIST Completes Document Preparation and Field Execution activities for the initial qualification activities for lab and/or Manufacturing equipment.

THE ROLE:
* Implements qualification program for initial qualification of laboratory and/or manufacturing equipment.
* This include document preparation for: Equipment Qualification Assessments (EQAs), Installation Qualifications (IQs), Operational Qualifications (OQs), and where applicable Performance Qualifications (PQs) and Summary Reports (SRs), Trace Matrices (TMs).
* This includes execution for IQ, OQ and where applicable, PQ.
* Maintain progress trackers for doc prep and execution activities.
* Attend daily co-ordination meetings with the Area Lead / QAVAL specialist / Associate Manager.

REQUIREMENTS:
* Proven experience in qualification of lab and/or manufacturing equipment, ideally in a bulk biologics start-up environment.
* Minimum Years of Experience: 3 years relevant experience.
* Minimal educational requirements: B.Sc or B.Eng.

Established in 1999, CareerWise Recruitment is recognised by many of the major indigenous and multinationals companies to be one of Irelands leading specialist Technical and Executive Recruitment firms.

We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway and Dublin.

Supporting Business Demands & Growth since 1999

CareerWise Recruitment accepts that you do not wish your CV to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will be respected at all times.