Staff Consumables Design Engineer

Danaher Corporation • Sunnyvale, CA

1d • $145,000 - $180,000

About The Position

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cepheid, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world’s most complex health challenges. Together, we bring MORE change to the world. Learn about the Danaher Business System which makes everything possible. The Staff Consumables Design Engineer is responsible for Designing, Testing, and Validating new consumable products in collaboration with multi-disciplined engineering teams. This includes translating product requirements into scalable, sustainable production of consumables parts and assemblies. This position is part of the R&D Consumables Team and will be located in Sunnyvale, CA. The R&D Consumables team spearheads the engineering of Cepheid’s consumable components (plastic parts). From designing new components, performing verification activities on design inputs, to validating quality of our product, this department plays a critical role in delivering products that meets or exceeds the customer’s need. In this role, you will have the opportunity to: Collaborate with Assay R&D, Chemistry R&D, R&D Lab Operations, Systems Integration, Technical Operations, and Quality to work on Innovation and New Product Development projects taking responsibility of full product development lifecycle from conception to product launch and transfer to Manufacturing. Document that the product meets production demand, customer needs and FDA requirements in a medical device environment. Enable consumables development using CAD, engineering drawings, finite element analysis, building prototypes, testing, part and equipment qualification and verification with an emphasis on defining part specifications, improving manufacturability, optimizing processes and achieving cost targets. Support the cross-functional teams with lab equipment and automation set up including vendor communications, fixture designs, standard operating procedures, control plans, test method development and quality control procedures.

Requirements

• Bachelor’s degree in engineering (Mechanical, Material Science, Plastics or related field) with 8+ years of related work experience or Master’s degree in field with 6+ years of related work experience or equivalent experience.
• Proven expertise in Plastic Injection Molding Part Design, Mold Design, Injection Molding Process development and Mold Qualification.
• Product life cycle experience, including design, test planning, execution, data analysis, associated documentation, and implementation to large-scale manufacturing in a medical device environment under design control processes.
• Strong analytical and troubleshooting experience, including understanding of system interfaces and quickly analyzing, tackling, and resolving system interoperability problems in ambiguous and complex situations to understand root cause and proficiency with data analysis software to conduct relevant analyses.
• Demonstrated leadership and collaboration when faced with various challenges, including but not limited to continuous improvement and problem-solving, in a cross-functional environment.

Nice To Haves

• Working knowledge of Polymerase Chain Reaction (PCR) or other biological applications of fluorescence-based techniques.
• Working with Finite Element Analysis Tools such as Ansys Mechanical and CFD.
• Metrology Method Development and Validation for Plastic parts and assemblies.

Responsibilities

• Collaborate with Assay R&D, Chemistry R&D, R&D Lab Operations, Systems Integration, Technical Operations, and Quality to work on Innovation and New Product Development projects taking responsibility of full product development lifecycle from conception to product launch and transfer to Manufacturing.
• Document that the product meets production demand, customer needs and FDA requirements in a medical device environment.
• Enable consumables development using CAD, engineering drawings, finite element analysis, building prototypes, testing, part and equipment qualification and verification with an emphasis on defining part specifications, improving manufacturability, optimizing processes and achieving cost targets.
• Support the cross-functional teams with lab equipment and automation set up including vendor communications, fixture designs, standard operating procedures, control plans, test method development and quality control procedures.

Benefits

• Cepheid, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.
• We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level