1

Biotech Operations Manager Jobs in Minnesota (NOW HIRING)

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... Ensure sustained compliance with the Quality Management System (QMS) and applicable regulatory ...

Project Manager II

Maple Grove, MN · On-site

$125 - $150/hr

... biotech or biopharmaceutical manufacturing environment, ideally pre‑clinical phases to commercial, or equivalent amount of experience managing commercial operations or client portfolio management ...

... Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our ... Provide GMP training and guidance to personnel involved in manufacturing and quality operations to ...

Supplier Quality Manager

Chaska, MN · On-site

$130K - $160K/yr

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... Directly manage Supplier Quality team in relation to supporting daily operations to meet customer ...

Supplier Quality Manager

Chaska, MN · On-site

$130K - $160K/yr

... biotechnology? AtBeckman Coulter Diagnostics, one ofDanaher's15+ operating companies, our work ... Directly manage Supplier Quality team in relation to supporting daily operations to meet customer ...

Buyer II

Bloomington, MN · On-site

$30 - $31/hr

This client is a German multinational Pharmaceutical and biotechnology company and one of the ... planning, supplier management, and inventory control to support operational needs. Key ...

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... This position will manage professional associates and operation support assigned to the Quality ...

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... This position will manage professional associates and operation support assigned to the Quality ...

Showing results 41-60

Biotech Operations Manager information

See Minnesota salary details

$30.4K

$62.1K

$116.1K

How much do biotech operations manager jobs pay per year?

As of Sep 8, 2026, the average yearly pay for biotech operations manager in Minnesota is $62,150.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,200.00 and $75,900.00 per year, depending on experience, location, and employer.

What does a Biotech Operations Manager do?

A Biotech Operations Manager is responsible for overseeing the daily operations of biotechnology facilities, ensuring that production processes run efficiently and comply with industry regulations. They manage teams, coordinate schedules, oversee supply chains, and implement quality control measures. Additionally, they work closely with research and development, regulatory, and quality assurance teams to ensure products meet all safety and efficacy standards. Their role is crucial in maintaining productivity, safety, and compliance in a biotech organization.

What are the key skills and qualifications needed to thrive as a Biotech Operations Manager, and why are they important?

To thrive as a Biotech Operations Manager, you need a solid background in life sciences, business management, and regulatory compliance, often supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and project management tools is typically required, along with certifications like Six Sigma or PMP being advantageous. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for managing teams and cross-functional projects. These skills ensure efficient operations, regulatory adherence, and successful product delivery in the highly regulated biotech industry.

What are some common challenges faced by Biotech Operations Managers, and how can they be addressed?

Biotech Operations Managers often face challenges such as maintaining regulatory compliance, managing cross-functional teams, and ensuring smooth production processes. These challenges can be addressed by staying updated on industry regulations, fostering clear communication between departments, and implementing robust quality control systems. Additionally, leveraging project management tools and continuous process improvement strategies can help streamline operations and minimize risks.

What is the difference between Biotech Operations Manager vs Biotech Laboratory Supervisor?

AspectBiotech Operations ManagerBiotech Laboratory Supervisor
CredentialsBachelor's or Master's in Life Sciences, Business, or related fields; experience in biotech operationsBachelor's or Master's in Life Sciences; laboratory management experience; relevant certifications often preferred
Work EnvironmentOversees multiple departments, manages projects, and ensures compliance across operationsManages daily lab activities, supervises lab staff, and maintains lab safety and procedures
Employer & Industry UsageUsed in biotech companies for operational oversightCommon in research labs, biotech firms, and pharmaceutical companies for lab management

The Biotech Operations Manager focuses on overseeing overall biotech operations, including project management and compliance, while the Biotech Laboratory Supervisor concentrates on managing daily lab activities and staff. Both roles require relevant scientific credentials, but their scope and responsibilities differ significantly.

What are popular job titles related to Biotech Operations Manager jobs in Minnesota?

For Biotech Operations Manager jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Biotech Operations Manager jobs?

Cities in Minnesota with the most Biotech Operations Manager job openings:

Infographic showing various Biotech Operations Manager job openings in Minnesota as of September 2026, with employment types broken down into 1% As Needed, 76% Full Time, 10% Part Time, 1% Temporary, 11% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $62,150 per year, or $29.9 per hour.

Senior Director Quality Operations

Danaher

Chaska, MN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 days ago


Key responsibilities

  • Provide strategic and operational quality leadership for manufacturing and development sites.

  • Ensure compliance with the Quality Management System and regulatory requirements, and lead continuous improvement initiatives.

  • Build, mentor, and develop the quality organization to meet site performance, compliance, and delivery goals.


Danaher rating

7.7

Company rating: 7.7 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

191st of 547 rated manufacturers


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 theDanaher Business Systemwhich makes everything possible.

The Senior Director, Quality Operations - Clinical Chemistry Immunoassay (CCIA) North America provides seniorlevel operational quality leadership for the Chaska, Minnesota and San Diego, California manufacturing and development sites, with accountability for manufacturing quality and development quality. This role translates enterprise quality strategy into disciplined site execution, ensures regulatory compliance, and drives a strong culture of quality across CCIA through close partnership with Operations, R&D, Supply Chain, and Regulatory Affairs.

This position reports to the Vice President, US Quality Operations and is a key member of the North America Quality Operations leadership team and will be based out of Chaska, Minnesota.

In this role, you will have the opportunity to:

  • Provide strategic and operational quality leadership for the Chaska site and Carlsbad sites, driving a strong culture of quality across the CCIA organization and establishing followership through influence and matrixed collaboration with crossfunctional partners.

  • Lead and be accountable for a complex, multidisciplinary quality organization, including Quality Assurance, Quality Control, Process Validation, Design Quality, Incoming Inspection, and sustained deployment of the Danaher Business System (DBS) to drive standard work, problem solving, and continuous improvement.

  • Ensure sustained compliance with the Quality Management System (QMS) and applicable regulatory requirements, partnering with global and local stakeholders to standardize, simplify, and continuously improve quality processes.

  • Own site quality performance and key performance indicators, proactively identifying gaps and leading structured problemsolving to resolution when performance is at risk.

  • Build and sustain an effective quality organization by ensuring appropriate staffing levels, clear role design, capability depth, succession coverage, and overseeing budget allocations required to consistently meet site performance, compliance, and delivery commitments.

  • Build, mentor, and develop strong, diverse teams and quality leaders, fostering engagement, accountability, and leadership behaviors that inspire followership and ownership at all levels of the organization.

  • Collaborate across all organizational levels, functions, and management chains to align priorities, communicate risk, and drive timely decisions to solution that protect patient safety and ensure the delivery of safe, compliant, highquality diagnostic products.

The essential requirements of the job include:

  • Bachelor's degree in a scientific or engineering discipline with 20+ years of experience, or Master's/Doctoral degree with 18+ years of experience, including 6+ years of people leadership experience.

  • Minimum of 10 years of quality leadership experience with invitro diagnostics or medical device industry, with direct accountability for manufacturing and/or development quality.

  • Demonstrated experience leading quality organizations at multisite or complex manufacturing environments, including responsibility for compliance, inspections, and operational performance.

  • Deep working knowledge of quality assurance, quality control, process validation, design quality, and supplier/incoming quality within regulated industries.

  • Strong understanding of IVD regulatory requirements and quality standards (e.g., FDA, ISO, global regulatory frameworks).

  • Proven ability to lead structured problem solving, apply data and riskbased decision making, and drive sustainable corrective actions.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel - up to 35% domestically and internationally per business needs.

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

  • Leading regulatory inspections, audits, or remediation activities in a regulated diagnostics or medical device environment.

  • Applying DBS or similar continuous improvement systems to improve quality performance and simplify processes.

  • Supporting new product introductions or product transfers, partnering with R&D and Operations to ensure compliant commercialization.

#LI-KW4

Beckman Coulter Diagnostics, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

The annual salary range for this role is $230,000 - $250,000. 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.

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.


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.


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.


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 applyassistance@danaher.com.


What Danaher employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Danaher logo

About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984