Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, 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. By harnessing Danaher’s system of continuous improvement, you help turn ideas into impact—innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our 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 continuously improve yourself and us by working on challenges that truly matter with people who care for each other, our customers, and their patients. Take your next step to an altogether life‑changing career. Learn about the Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible.
Responsibilities
- Identify, participate in and lead projects that deliver improvements in safety, quality, delivery and cost
- Problem‑solve process issues and/or product non-conformances using empirical evidence and quantitative analysis
- Participate in new product development projects and support the transfer of new products from development into production
- Create process and validation documentation to ensure manufacturing is performed safely and meets documented quality specifications
- Provide technical and project leadership to develop and deploy equipment and process upgrades for new product development, cost reduction and quality improvement
Qualifications
- Bachelor’s degree in Mechanical, Manufacturing or Process Engineering (or a related field) with more than 5 years of relevant experience
- Experience applying lean manufacturing tools including daily management, standard work and lean conversion
- Experience with equipment and process design and improvement in a regulated industry
- Excellent written and verbal communication skills, comfortable interacting at all levels of the organization
- Able to work independently and collaborate well across diverse functions in a matrix organization
- Travel requirements: Able to travel within UK/Europe in support of the role objectives (estimated at 10%)
- Must have a valid driver’s license with an acceptable driving record
- Preferred: Clean‑room experience in the pharmaceutical or medical device industry
- Preferred: Formal training, qualification and proven experience in Six Sigma techniques
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.
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