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.
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The Product Transfer Assay Life Cycle Division, part of Technical Operations, acts as technical partner to several Swedish and international functions within Cepheid. We lead and coordinate post-launch changes, improvement projects, transfers of assays between manufacturing sites, and support expansions into new markets. As part of these activities, we solve problems and develop new processes, methods, and procedures, assuring manufacturability and continued production of cost-effective high-quality products.
In this role, you will have the opportunity to:
- Work with changes that affect Cepheid's market products. You will lead and participate in Product Life Cycle projects
- Represent the Product Transfer function to ensure compatibility with manufacturing processes and capabilities, as well as serve as technical liaison for other departments.
- Work on projects focused on medical device reagents, enzymes, and plastic consumables and will enrich the team with your expertise and experience in consumables failure investigation, troubleshooting, and development.
- Have Daily interaction with Operations, Quality Control, Regulatory, R&D, Global Supply, and other national and international functions within Cepheid.
- Design and execute Verification and Validation (V&V) as well was qualification studies.
- Continuous production of cost-effective and high-quality products through effective implementation of changes to both products and processes, participation in improvement initiatives, transfers of assays between manufacturing sites and expansions into new markets.
The essential requirements of the job include:
- PhD in Life Sciences with 2+ years of relevant professional experience, or MS in Life Sciences with 6+ years of relevant professional experience
- Proficiency in Molecular Biology (PCR/RT-PCR) and Protein Biochemistry
- Experience in Reagents, Enzymes, and Consumables Development, Qualification, Investigation, and/or troubleshooting.
- Experience in Project Management within a global organization. Deep and broad expertise in Risk and Change Management.
- Excellent level of Swedish and English, written and oral.
It would be a plus if you also possess previous experience in:
- Work experience within Operations or Manufacturing
- Experience with Design for Manufacturing, Design Verification, Design Validation, Qualification, Risk Assessment
- Experience from working in a regulated environment (ISO/GMP)
Cepheid, a Danaher operating 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.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
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