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Cepheid, a Danaher operating company, seeks a Senior Product Stability Specialist to drive stability strategies for GX assay products across development and post-launch phases. This on-site role is based in Sunnyvale, CA and emphasizes cross‑functional collaboration to deliver timely results.
You will develop stability plans, write plans and reports, and guide investigations and method validations, reporting to the Sr Manager Assay NPD Quality Assurance in Sunnyvale.
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 Senior Product Stability Specialist is responsible for solving complex problems, take a broad perspective to identify innovative solutions and work independently with guidance in only the most complex situations. This person plays a key role in providing technical quality support throughout the life cycle of GX assay products.
Key activities are developing stability strategies with emphasis on assay development and post launch activities, write plans and reports, provide guidance for investigations, test method development and validations.
This position reports to the Sr Manager Assay NPD Quality Assurance and is part of the Quality Assurance and Regulatory Affairs NPD located in Sunnyvale, California and will be an on‑site role.
In this role, you will have the opportunity to:
Bachelor’s degree in field with 5+ years of related work experience within a medical device or pharmaceutical industry, MS in Life Sciences with 3+ years of relevant professional experience, or Ph.D in Life Sciences with 0-2 years of relevant professional experience. Knowledge of cGMP, ISO, and FDA regulations Proficiency in Molecular Biology Techniques including PCR Experience in working in cross‑functional teams in a global environment Travel, Motor Vehicle Record & Physical/Environment Requirements: Work in a laboratory environment
It would be a plus if you also possess previous experience in:
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