Quality Engineer, Wicklow

CPL

Wicklow

Reporting to the Head of Quality and Technical Affairs, the successful candidate will be responsible for providing guidance on all aspects of quality, validation and quality engineering within a cross functional team thus ensuring customer satisfaction and reduction of scrap. Principal Duties and Responsibilities: The main duties include but are not limited to the following: • Support Operations through the product life cycle / process for defined product portfolios. • Management of process deviations, non conformances, reworks, CAPA, Design Changes, complaints, scrap and change requests for product group. • Lead Validation activities for designated product groups. • Conduct process and GMP audits and ensure area compliance. • Liaise with regulatory department to ensure product supply is maintained and all quality aspects are met. • Champion QA and continuous improvement initiatives. Applications are invited from candidates with the following background and experience: • Graduate in a science, engineering or related background. • Minimum 5 years in a QA Engineering / QE role, working within a recognised quality system within IVD, Medical Device or Pharma industry. • Minimum 3 years validation experience in equipment/process/software is highly desirable. • A working knowledge of regulatory requirements. • A technical background or knowledge of IVD products or Medical devices would be advantageous. • Awareness of statistical techniques and validation. • Experience of internal, third party regulatory & external customer audits. • A high degree of computer literacy. For a full Job Spec and to apply for this role please forward your CV in strict confidence to dbolger@thornshaw.com or call Deirdre on +353 1 2784671. Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671. This job originally appeared on RecruitIreland.com.

2580 days ago