|
Staff Automation Engineer - Wilton California
Company: Cepheid Location: Wilton, California
Posted On: 04/24/2024
At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we're working at the pace of change on diagnostic tools that address the world's biggest health challenges, driven by knowing that behind every test there is a patient waiting.Learn about the which makes everything possible.The Staff Automation Engineer is responsible for the design, development, documentation, and production launch of complex, high speed assembly equipment. This equipment will be used in the high-volume production of diagnostic biomedical devices consumables. The successful candidate will be responsible for system specification, machine tooling and fixture design. Hands on and supervisory experience of automated equipment assembly, electro-mechanical equipment and mechanical design of prototype fixtures is required. Position also requires interacting with contract manufacturers for outsourced projects.This position is part of the Automation Development Engineering team and will be located in Lodi, CA. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions.In this role, you will have the opportunity to: - Responsible for the design and development of automation projects including, initial concept, design requirements, system architecture, test plan, prototype fabrication testing and final production release.
- Create detailed documentation including but not limited to design input requirements, specifications, design of experiments, acceptance test and validation protocols, detailed drawings, and bills of materials.
- Selection and specification of machine components such as motors, pneumatics, conveyors, and part feeding components.
- Modify existing equipment to improve product quality, increase part throughput, decrease cost, and/or strengthen safety measures.
- Evaluate and recommend engineering changes to equipment or processes that will ensure maximum productivity.The essential requirements of the job include:
- BS in Mechanical Engineering (or a related field) with 8+ years of experience within medical device or a regulated industry OR MS in Mechanical Engineering (or a related field) with 6+ years of experience within medical device or a regulated industry
- Strong analytical and problem-solving skills combined with a strong technical presence.
- Proficient in SolidWorks 2019 or later, PDM or EPDM.
- Working knowledge and experience of GMP, ISO, and FDA rules and regulatory requirements
- Ability to work in clean room environment, use hand or power tools, and be able to stoop, kneel, crawl, lift, push.It would be a plus if you also possess previous experience in:
|
|