Senior Manufacturing Scientist Wondering what’s within Beckman Coulter Diagnostics? Take a closer look. At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. The Senior Manufacturing Scientist for Beckman Coulter Diagnostics is responsible for supporting the daily production needs of a Reagent manufacturing work cell. This includes investigation and resolution of assay failures during in-process/pre/post fill reagent testing, maintenance of bills of materials and material specification changes due to new material qualification or supplier changes, and updating/correcting SOPs in compliance with current quality system standards. There will be opportunities to tackle problems to keep reagents moving through the value stream to serve our customers with high-quality finished goods. This position is an integral part of the Reagent Operations department located in Chaska, Minnesota, and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Technical Operations team and report to the Manager, Manufacturing Science, responsible for conducting investigations, document updates, design changes, troubleshooting, and more. If you thrive in a fast-paced and data-driven role and want to work to build a world-class manufacturing organization—read on! In this role, you will have the opportunity to: + Provide technical expertise and direction in multiple Immunoassay manufacturing areas. + Lead multi-department teams to support/resolve non-conforming issues for existing products. + Assess manufacturing processes and systems and implement improvements aimed at performance, quality, and cost. + Communicate investigation status reports, proposals for further investigation, etc., via oral and written reports; Develop and implement changes to existing documentation in a timely manner. + Solve immunoassay testing and manufacturing issues as they arise. The essential requirements of the job include: + Biochemistry, chemistry, or biology (or related field) Bachelor’s degree with 5+ years of industry experience or Master’s degree with 3+ years of industry experience or Doctoral degree + Experience in a regulated industry preferred (e.g. FDA, ISO) + Strong technical understanding of biochemical/immunoassay processes and experience analyzing and interpreting data. + Experience discussing technical concepts with a diverse audience, including experts and non-experts. + Extensive knowledge with Microsoft applications, including Word, PowerPoint, Excel, and the basic Windows operating system. It would be a plus if you also possess previous experience in: + Project Management experience + Manufacturing of biologicals or pharmaceuticals + Validation/verification experience The salary range for this role is 98-115K. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law. #LI-NS3 #LI-Onsite 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 . 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.