Supervisor Cell Culture and Purifications Manufacturing
Beckman Coulter Diagnostics

Job Info

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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 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 Supervisor Production Operations - Cell Culture and Purifications for Beckman Coulter Diagnostics is responsible for supervising the mammalian cell culture and protein purification teams. These teams produce and purify monoclonal and polyclonal antibodies for use in immunodiagnostic test kits.

This position is part of Immunodiagnostics Production Operations located in Chaska, Minnesota and will be an on-site position. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.

You will be a part of the Upstream Reagent Formulations Team and report to the Manager of Reagent Formulations responsible for the production and purification of antibodies, and the generation of conjugates and coated particles. If you thrive in a collaborative and inclusive technical leadership role and want to work to build a world-class manufacturing organization-read on.

In this role, you will have the opportunity to:

• Lead a technical team of Cell Culture and Protein Purification scientist to achieve their best while assuring compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements
• Work in coordination with cross-functional team members to tackle problems and implement manufacturing improvement ideas
• Identify and recommend quality improvements to processes including but not limited to production methods, equipment, product quality and efficiencies

The essential requirements of the job include:

• Bachelor's degree with 5+ years' experience, or master's degree with 3+ years' experience.
• Experience directly or indirectly leading a team
• Organizing and tracking training for team members as well as completing documentation, maintain accurate records of production and report status of work.

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

• Proficiency with aseptic techniques, mammalian cell culture, protein purification and protein characterization techniques
• Understanding of large-scale bioreactor systems, FPLC, HPLC and protein characterization methods.
• Familiarity with in vivo and in vitro antibody/antigen production.
• Validation/verification experience
• Experience in a regulated industry preferred (e.g. FDA, ISO) with advanced knowledge of cell culture production and/or purification techniques.

This job is 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.

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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.

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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.

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