We have a new contract opportunity for a manufacturing engineer to coordinate, create, develop, design and improve products in conformance with established programs and objectives.
This is initial 6 months contract (with possibility of extension) in Switzerland.
Providing direction and leadership in line with operational strategies and objectives to support existing and new production facilities and processes. Managing a team of engineers in support of industrial manufacturing processes designed to promote lean manufacturing, demand flow, work efficiency and cost savings. Planning , scheduling, managing and monitoring smooth execution of various engineering projects, ensuring adherence with all local government and company regulations, policies and procedures for environment, health and safety compliance. Ensures the documentation of project and program activities and deliverables. Supporting implementation of new product development plans for the business unit. Develops industrial engineers and technicians as strong contributing members of extended NPI teams (New Product Introduction). Reviewing and approving technical documentation to verify compliance technical specifications and standards. Planning and managing cost improvement program related to manufacturing engineering. Overseeing overall capital expenditures program for the business unit, responsible for the development and justification of the engineering department capital investments. Setting business metrics for the team and provides performance feedback to employees. Overseeing a department for technical engineering work such as CAD, tooling, fixture design, and technical documentation.
University/Bachelor Degree in Engineering or equivalent Prior experience in industrial manufacturing engineering in the medical device or regulated industry Interpersonal skills / characteristics: Strategic agility, knowledge of business planning: ROI, Value proposition & Profit optimization Good knowledge of lean manufacturing principles. Cross-functional project management experience to develop and transfer new product and/or technology into manufacturing required. Excellent knowledge and understanding of the medical device quality system regulation required (ISO & QSR).
Please send your CV
Michael Bailey International is acting as an Employment Business in relation to this vacancy.