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 one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. The QC Technician role will support Cytiva’ s new plant for manufacturing of chromatographic resins located in Muskegon, MI. This role will play a key part in the start-up and establishment of Laboratory Operations to support all parts of manufacturing from raw material testing to product release including troubleshooting activities. You are expected to travel outside of US as the Muskegon site cooperates with Uppsala site in Sweden. Your duties vary from daily operations in the Laboratory where you will perform analytical experiments, hands on problem solving, documentation, and report results. What you’ll do: + Be a part of the ongoing Transfer and Build Project to establish the Quality Control Laboratory at the Muskegon site. + Write and review analytical methods and instructions to be used in testing and analysis. + Perform, calibrations, maintenance, and deviation management according to the Cytiva Quality Management System. Who you are: + Minimum Bachelor degree from an accredited University or College in Chemistry, Biochemistry, Microbiology or applicable. An Associate’s degree with 5 plus years working experience in a Quality Control Laboratory may be substituted in lieu of a Bachelor degree. + Minimum 2 years working experience in a Quality Control Laboratory. + Good documentation (GDP & GMP) skills with the ability to transfer information in both written (Microsoft Office Suite) and verbal environments. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.