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Danaher Corporation Regulatory Compliance Leader in Cardiff, United Kingdom

Be part of something altogether life-changing

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

What you'll do

  • Support the development of new products within the Cytiva portfolio

  • Author SDS (Safety Data Sheets) for new products and revise SDS for existing products

  • Review change requests/orders to ensure that compliance requirements are met and maintained

  • Core team member for New Product Introduction (NPI) projects to secure compliance to relevant regulations to get market access

  • Maintain awareness of applicable regulations, and monitor activities related to changes to regulations

  • Participate/support Project Management Office (PMO) projects

  • Supporting the Operations Leaders within the Product and Technology Compliance team to form and drive strategies

  • Drive compliant, simple, cost-efficient and pragmatic solutions to issues related to regulatory requirements in NPI’s and other projects

    Who you are

  • Bachelors' Degree in Chemistry, Biochemistry, Biologics or related discipline

  • 3 + years relevant working experience

  • Experience with Product regulations, QA/RA, biological materials, other regulatory areas or experience with Cytiva’s product portfolio and an interest to learn about regulatory compliance

Preferred qualifications

  • Knowledge around the Cytiva portfolio

  • Knowledge around environmental, chemistry and biological regulations, e.g. familiar with REACH, GHS labeling, hazardous chemicals, Safety Data Sheets

  • Experience in communicating with authorities, e.g. chemistry and border control authorities

  • Experience with SDS tools, e.g. ChemMate

When you join us, you’ll also be joining Danaher’s global organization, where 68,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.

Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we’ll empower you to push the boundaries of what’s possible.

If you’ve ever wondered what’s within you, there’s no better time to find out.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here (http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf) .

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