What are the responsibilities and job description for the Quality Control Supervisor position at Beckman Coulter, Inc.?
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 Quality Control Supervisor for Beckman Coulter Diagnostics is responsible for management and technical support for the Incoming Inspection and Manufacturing QC departments.
This position is part of the Quality Group 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 Quality Team and report to the Sr. Quality Assurance Manager responsible for people leadership of Quality Control Technicians. If you thrive in a leadership role and want to work to build a world-class quality organization—read on.
In this role, you will have the opportunity to:
- Engage and develop talent of the team by training, coaching and modeling behaviors.
- Identify and communicate problems that might affect the quality of integrity of the product and work to resolve issues.
- Resolve routine but technically complex problems using defined processes and coordinates resources to meet short-term objectives
The essential requirements of the job include:
- Bachelor’s degree with 5 years experience, or Master’s degree with 3 years. Field of Science or Engineering preferred.
- Direct experience working in a Quality role or testing lab strongly preferred FDA regulated environment experience.
- Demonstrated leadership skills with ability to manage team by influence.
- Knowledge and application of Lean Manufacturing and statistics.
- Fundamental knowledge of medical industry practices.
It would be a plus if you also possess previous experience in:
- Direct supervision of associates.
- FDA, QSR/cGMP, and ISO 13485 standards and regulations
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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For more information, visit www.danaher.com.
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