Scientist II Production Operations

MedDeviceJobs; Chaska (MN); On-site; USD 66,000 - 78,000; Full time

Benefits offered by this job

Bonus eligible

Job summary

Beckman Coulter Diagnostics, a Danaher company, is seeking a Scientist II Production Operations in Chaska, MN to execute the daily production plan and maintain a smooth flow of material in a fast-paced manufacturing environment.

You will follow SOPs, ensure compliance with FDA QSR, GMP and ISO requirements, and apply basic analytical methods while collaborating with cross‑functional teams to troubleshoot issues and uphold quality.

Qualifications

• Bachelor’s degree in a Science field with 3+ years experience or Master’s with 1-2+ years experience.
• Proven track record of good laboratory practices and adherence to SOPs.
• Familiarity with FDA, GMP, and ISO regulatory requirements.

Responsibilities

• Execute the daily production plan to meet due dates and quality standards.
• Buffer and reagent preparation following good laboratory practices.
• Ensure compliance with QSR, GMP, and ISO requirements.
• Apply analytical methods to daily tasks and troubleshoot with cross‑functional teams.

Skills

GLP experience

SOP adherence

FDA/GMP/ISO compliance

Analytical skills

Cross-functional collaboration

Education

Bachelor’s Degree in Science

Master’s Degree in Science

Tools

DxI800

DxI9000

Access II

Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Beckman Coulter Diagnostics, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory’s role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible.

The Scientist II Production Operations for Beckman Coulter Diagnostics is responsible for following established operation procedures, maintaining appropriate training records for your role, sustaining a smooth flow of material, and the execution of work orders to on-time completion.

This position reports to the Supervisor of Reagent Operations and is part of Reagent Operations department located in Chaska, MN, and will be on-site. If you thrive in a fast-paced dynamic role and want to work to build a world-class manufacturing organization—read on.

In this role, you will have the opportunity to:

• Execute the daily production plan to due date conformance and quality standards according to Standard Operating Procedures (SOPs)
• Independently execute work regarding buffer and reagent preparation using good laboratory practices; assistance in other areas as needed
• Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements
• Apply basic analytical skills or scientific methods to perform daily tasks
• Work directly and cooperatively with cross-functional team members to troubleshoot issues and ensure emphasis on quality

The essential requirements of the job include:

• Bachelor’s Degree in a Science field / 3+ years of relevant experience or a Master’s degree in a Science field with 1-2+ years or relevant experience
• Proven track record of good laboratory practices (GLP).
• Proficient in executing manufacturing processes, strictly adhering to SOPs, written/verbal specifications, and all relevant FDA, GMP, and ISO regulatory requirements

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

• A regulated industry preferred (e.g. FDA, ISO)
• Updating and improving SOPs to reflect current best practices and operational changes
• Testing utilizing Access II, DxI800, and DxI9000 Instruments

The salary range for this position is: $66K-$78K. 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.

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.

The U.S. EEO posters are available here (http://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12ScreenRdr.pdf) .

For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here (https://jobs.danaher.com/global/en/notice-to-us-candidates-based-in/applying-for-roles-outside-nyc) .

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or [e-mail].