Quality Engineer, Validation Consultant

Job Role:

This Quality Engineer role will be dedicated to a 6 months project to resolve a CAPA backlog and internal audit observations.

Role Responsibilities:

• Support the operations team for the management of quality activities: CAPA, audit observations.
• Support the operation team for Audit Preparation & Readiness Provide support during internal and external audits (FDA, BSI, MDSAP, Lean, EHS, etc.)
• Lead and follow continuous improvement projects.
• Formal authority to: Review, investigation and approval of CAPA / NC. - Create and approve Cos

Job Requirements:

• Engineer with quality background and 2-3 years of experience in managing CAPA.
• University degree in Engineering or equivalent
• Good knowledge of production environments Mastery of CAPA management tools, problem-solving
• Good mastery of project management tools
• Excellent computer skills
• Experience in the Medical Device sector

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Caleb Mensah on +44 203 854 1080 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.