Description
A leading global pharmaceutical organisation requires a QA Engineer SME (Subject Matter Expert) to join their team at their Biotech manufacturing facility based in Italy. You will be required to ensure the facility is compliant with all GMPs, SOPs and Corporate policies and practices.The Role:
-Working as an SME (Subject Matter expert) for QA and compliance
-Responsible for gap analysis audits of the equipment and facilities of biotech manufacturing campus to ensure engineering activities are performed in a manner that is compliant.
Experience:
-GMP / GEP / Biotech / Engineering background - essential
-Extensive experience within the pharmaceutical industry - essential
-Previous experience of working as a Senior QA Engineer Lead / SME
-Compliance - Lead / Management experience
-Experience of Internal and supplier audits
-Experience within team leadership, management, engineering systems design and implementation. As well as Pharmaceutical design, commissioning/qualification and validation.
-Fermentation / Purification experience - essential
-Languages: English and Italian (Italian highly desirable)
A fantastic rate is available alongside an exceptional opportunity to join a global pharmaceutical organisation.
Please apply today with a covering letter highlighting your key skills and relevant experience aligned to this contract opportunity.