Description
Quality Assurance Officer
One of the world`s leading biotechnology organisation based in Belgium requires a Quality Assurance Officer to join their 250 million new build based in Belgium. The QA Officer will work closely with manufacturing, validation engineering, quality control, technology and logistic departments to assure compliance.
The role:
.Participates in internal audits and inspections as well as in conducting follow-up to non-compliance issues.
.Audits/inspections may include cGLP, cGMP, cGCP and/or in-house compliance evaluations.
.Reads and interpret documentation for new and current compliance procedures and regulatory enforcement trends/actions. Participate in the preparation and review of procedures.
.Participates in determining corporate quality and compliance policies.
.Complete analysis, identifies issues and provides recommendations for compliance improvements.
.Evaluates and signs off on documents related to area of expertise
.Assists supervisor and manager during regulatory inspections
.Record review (validation documentation, protocols/reports for IQ, OQ and PQ)
Experience:
.Experience of working Biotech start-up/project
.Experience in QAV - Quality Assurance Validation
.Good working knowledge of cGLP/cGMP/cGCP in a regulated environment.
.European regulations/US regulations
.Good working knowledge of manufacturing/QC/TY/PL/F&E processes and the application of quality principals.
.Excellent accuracy and attention to detail.
An excellent daily rate is on offer alongside an opportunity to work for one of the world`s leading biotechnology organisations.
Please contact - Rebecca Church