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 North America Document Services Supervisor for Beckman Coulter Diagnostics is responsible for coaching, motivating, and leading the team to accomplish the productivity goals for the project milestones and establishing a culture of positive employee relations while ensuring all processes, best practices and policies are adhered to consistently.

This position is part of the North America Document Services team and will be located in Chaska, MN onsite. At Beckman Coulter, our vision our vision is to relentlessly reimagine healthcare, one diagnosis at a time.

You will be a part of the North America Document Services team and report to the Senior Manager for Technical Documentation. You will be responsible for establishing and maintaining product coaching, motivating, and leading the team to accomplish the productivity goals for the project milestones and establishing a culture of positive employee relations while ensuring all processes, best practices and policies are adhered to consistently. If you thrive in a fast-paced leadership role and want to work to build a world-class Document Services organization—read on.

In this role, you will have the opportunity to:

• Supervise, engage and develop talent of the team by training, coaching and modeling behaviors to meet daily and project deliverables.

• Handle day-to-day challenges, show flexibility in approach to meet multiple project demands and prioritize daily/weekly work assignments to meet production needs for staff through strong partnership with staff, project and operations teams.

• Measure and monitor work of both self and team to ensure compliance to quality systems with adherence and integrity in a regulated environment through compliance to all FDA, QSR/cGMP, ISO and Quality Policies of Beckman Coulter.

• Resolve routine but technically complex problems using defined processes and coordinate resources to meet short-term objectives.

• Lead performance and development goals for direct reports.

• Act as subject matter expert during internal and external audits. Responsible for investigating and completing actions related to the audit findings.

• Recommend and implement system enhancements as needed that result in more effective quality operations as well as improve the end user experience.

The essential requirements of the job include:

• High School degree with 8+ years of experience or Bachelor’s degree with 5+ years of experience or Master’s degree with 3+ years of experience.

• 2 or more years leading teams and or previous supervisor experience.

• Experience in an FDA regulated environment and with regulations associated with document control and product labeling for medical devices.

It would be a plus if you also possess previous experience in:

• Oracle, Adobe Acrobat, EDMS, ENOVIA & Solid Works.

• Experience in a Document Control or change order environment.

• Practical understanding of IT processes associated with document management and document publication.

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.

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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.