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Plastic Tooling Process Engineer II - Chaska
Plastic Tooling Process Engineer II - Chaska-January 2024
Chaska
Jan 13, 2026
About Plastic Tooling Process Engineer II - Chaska

  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 the 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 Plastics Process Engineer II will be responsible for leading and executing projects related to the design and development of plastic medical devices, ensuring that the products meet quality, cost, and delivery requirements. This will involve working closely with cross-functional teams such as R&D, manufacturing, Quality, and Supply Chain. This position is a hybrid role located in Chaska, MN.

  In this role, you will have the opportunity to:

  Ensure projects are completed on time, within budget, and to the required quality standards, with a focus on medical device industry requirements and validation processes

  Work with project teams and collaborate with cross-functional teams to resolve technical issues.

  Implement processes and tools to improve product quality and efficiency, with a focus on medical device industry requirements.

  Ensure that all design and development activities are following industry standards and regulations, including medical device industry requirements.

  Generate design change documents, perform risk analysis, and design transfer activities as needed.

  The essential requirements of the job include:

  Bachelor's degree in Mechanical, Plastics or Manufacturing Engineering.

  3+ years of experience in plastics tooling and manufacturing processes.

  Project management skills and experience working with cross-functional teams.

  Understanding of validation requirements and processes applicable to the medical device industry.

  Knowledge of quality systems and experience in continuous improvement.

  #LI-MR1

  When you join us, you’ll also be joining Danaher’s global organization, where 80,000 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 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 [email protected] to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out.

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