Shift Process Engineer

Lumiradxukaccount ,
Alloa, Clackmannan
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Job Description

Shift Process Engineer This role will initially work a shift of 06:30-15:00 1 week and 14:30-22:30 the next week. We plan to move to 24/7 shifts later in 2020 (exact shift pattern to be confirmed). LumiraDx is a medical technology company developing, manufacturing and marketing smart connected diagnostics and diagnostic-led care solutions. Founded in 2014 by entrepreneurs with a successful track record in building and scaling medical diagnostics and health IT businesses, the company has major operations in the UK and the USA, and is supported by a global sales network, LumiraDx currently has over 600 employees worldwide. We have recently launched the innovative LumiraDx Platform, and are looking for proactive, experienced, focused and enthusiastic individuals who can make a significant contribution to the continued growth and success of our dynamic and forward-looking company. Role Description An experienced Process Engineer who can make a significant contribution to the continued growth and success of our company. As a Process Engineer you will support all aspects of the Reel to reel print line and automated manufacturing processes. Providing support to Manufacturing, Quality and Equipment Engineering through process monitoring and continuous improvement activities. Key Responsibilities * Product and process performance monitoring. * Troubleshooting, rapid diagnosis and resolution of problems in existing manufacturing plant & processes, using a methodical approach and report progress in a structured way. * Statistical analysis, trend monitoring and reporting. * Determine, categorise and develop mitigation for failure modes. * Develop & improve manufacturing methods utilising knowledge of product design, materials, fabrication processes, tooling and production equipment assembly methods. * Investigate, root cause & resolve Non-Conformances / Quality Events. * Be open to self-development and the development of others during the transition from R&D through to volume manufacture. * Adhere to all relevant regulatory requirements. * Engage the production team in the identification of cost and inventory reduction initiatives, whilst also striving to streamline workflow. About you You will be highly motivated engineer and have excellent proven experience in continuous improvement in a regulated environment with a strong knowledge of how to use data to help improve performance. Other requirements to be successful in this role are as follows: * A hands-on Process Engineer with a high level of relevant industry experience. * Experience of optimising product and processes, medical would be an advantage. * Knowledge of statistical process controls, capabilities and analysis techniques. * Experience of executing GRR (gage repeatability and reproducibility) protocols. * Experience of executing product and process verification protocols. * Experience of Design of Experiments. * GMP experience. * High level of computer literacy in MS Office. * Competent in documentation and report writing. Apply for this Job

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