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Biotech Quality Control Jobs in Minnesota (NOW HIRING)

Harvard Bioscience

Quality Manager ISO9001

Saint Paul, MN · On-site

$110K - $160K/yr

... pharmaceutical, biotechnology and clinical research organizations. POSITION SUMMARY Harvard ... Supports manufacturing change control projects. * Reviews exception proposals as part of risk ...

Harvard Bioscience

Quality Manager ISO9001

Saint Paul, MN · On-site

$110K - $160K/yr

... pharmaceutical, biotechnology and clinical research organizations.POSITION SUMMARY Harvard ... Supports manufacturing change control projects. Reviews exception proposals as part of risk ...

Microbiologics, Inc.

R&D Scientist

Saint Cloud, MN · On-site

$86K - $107K/yr

  • Medical

  • Dental

  • Life

  • Retirement

As a well-established biotechnology company with a strong reputation for quality, collaboration ... You will help shape next-generation control materials and biomaterials that support pharmaceutical ...

Microbiologics

R&D Scientist

Saint Cloud, MN

  • Medical

  • Dental

  • Life

  • Retirement

As a well-established biotechnology company with a strong reputation for quality, collaboration ... You will help shape next-generation control materials and biomaterials that support pharmaceutical ...

Danaher

Staff Quality Assurance-Supplier Quality Engineer

Chaska, MN · On-site

$77K - $99K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... records, change control documentation, and support files- measured by clear, audit-ready ...

Danaher

Senior Supplier Quality Engineer

Chaska, MN · On-site

$0.05 - $0.06/hr

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... Develop supplier material control plans as part of product qualification * Primary supplier quality ...

Teleflex

Laboratory Technician 2

Maple Grove, MN · On-site

$19.50 - $25.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Specialized Skills / Other Requirements • GMP QC laboratory experience for pharmaceutical, biotechnology or medical devices industry highly preferred. • Experience with pipetting, dilution and ...

Teleflex

Laboratory Technician 2

Maple Grove, MN · On-site

$19.50 - $25.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Specialized Skills / Other Requirements GMP QC laboratory experience for pharmaceutical, biotechnology or medical devices industry highly preferred. Experience with pipetting, dilution and reagent ...

Oncodea

Molecular Diagnostics Associate

Saint Paul, MN · On-site

  • Medical

  • PTO

Run routine molecular pattern acquisition and QC; help refine and troubleshoot the analytical ... One or more years of combined experience across academic research labs, biotech industry, or ...

Syngenta Group

Production Technician

Cokato, MN · On-site

$45K - $68K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotech crops that can thrive even in challenging growing conditions. Syngenta Seeds is ... Demonstrate knowledge of and adherence to company's Quality Assurance/Quality Control (QA/QC) ...

Syngenta

Production Technician

Cokato, MN · On-site

$45K - $68K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotech crops that can thrive even in challenging growing conditions. Syngenta Seeds is ... Demonstrate knowledge of and adherence to company's Quality Assurance/Quality Control (QA/QC) ...

Syngenta Seeds

Production Technician

Howard Lake, MN

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotech crops that can thrive even in challenging growing conditions. Syngenta Seeds is ... Demonstrate knowledge of and adherence to company's Quality Assurance/Quality Control (QA/QC) ...

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Showing results 21-40

All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Minnesota

Biotech Quality Control information

See Minnesota salary details

$29.9K

$79.6K

$126.8K

How much do biotech quality control jobs pay per year?

As of Aug 19, 2026, the average yearly pay for biotech quality control in Minnesota is $79,649.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,300.00 and $97,900.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are popular job titles related to Biotech Quality Control jobs in Minnesota?

For Biotech Quality Control jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Biotech Quality Control jobs in Minnesota look for?

The top searched job categories for Biotech Quality Control jobs in Minnesota are:

What cities in Minnesota are hiring for Biotech Quality Control jobs?

Cities in Minnesota with the most Biotech Quality Control job openings:

Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Minnesota as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 100% In-person job distribution, with an average salary of $79,649 per year, or $38.3 per hour.

Quality Manager ISO9001

Harvard Bioscience

Saint Paul, MN • On-site

$110K - $160K/yr

Full-time

Posted 28 days ago

Job description

ABOUT HARVARD BIOSCIENCE
Harvard Bioscience is a leading global developer, manufacturer and seller of technologies, products and services that enable fundamental research, discovery, and pre-clinical testing for drug development. Our customers range from renowned academic institutions and government laboratories, to the world's leading pharmaceutical, biotechnology and clinical research organizations.
POSITION SUMMARY
Harvard Bioscience is looking for a Quality Manager for our New Brighton office. This role is responsible for executing the Global Quality Plan, driving cultural changes toward Quality processes, and collaborating with production, product development, sales/marketing, and post-market teams to ensure connection with processes and data.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Leadership:
  • Support and expand the culture to provide high quality products to customers.
  • Provide mentorship to quality team and department leads.
  • Cultivate collaborative culture across the organization.
  • Manage the Quality Management System architecture to meet corporate needs.
  • Reviews Quality System operation and identifies improvements.
  • Plans and leads improvement projects.

Quality:
  • Leads execution of the Global Quality Plan in Holliston.
  • Tracks regulatory changes and makes recommendations for system changes.
  • Leads the CAPA review board, including field risk assessment.
  • Plans and executes Internal Audit schedule.
  • Responds to external information requests (customers, audits).
  • Provides perspective and experience for information management procedures and tools.

Operations:
  • Supports validation of manufacturing processes.
  • Supports manufacturing change control projects.
  • Reviews exception proposals as part of risk assessment.

Design:
  • Supports project, verification, and design validation planning.
  • Supports design change control projects.

SKILLS AND ABILITIES REQUIRED
  • Strong organization, communication, and leadership skills.
  • Knowledge of relevant manufacturing and process development principles and practices.
  • Project management skills, ability to plan, and perform against plan.
  • Interpersonal and leadership skills with the ability to establish rapport with cross functional team members to create high performance teams.
  • Confidence to provide quality staff direction and assignments consistent with department objectives and priorities.
  • Ability to review the manufacturing processes, design verification plans and reports, and process validation/qualification protocols and reports.
  • Full understanding of ISO 9001:2015 Required.
  • Experience with ISO 13485:2016, ISO 14971:2019, IEC 62366-2:2015 or other regulations a plus.
  • Willing to share knowledge and teach others about processes.
  • Knowledge of the full product lifecycle (Launch/Maintain/Obsolete).
  • Ability to work effectively in a cross-functional team environment.
  • Strong analytical ability with active listening skills.
  • Ability to interpret and articulate regulatory requirements.
  • Ability to lead by example.

EDUCATIONAL REQUIREMENTS AND/OR EQUIVALENT
4-year engineering degree with 5+ years relevant experience and 2+ years of management experience preferred.
AN EQUAL EMPLOYMENT OPPORTUNITY EMPLOYER/VETERAN/DISABILITY
FLSA: Exempt
ADA DISCLAIMER
In developing this job description care was taken to include all competencies needed to successfully perform in this position. However, for Americans with Disabilities Act (ADA) purposes, the essential functions of the job may or may not have been described for purposes of ADA reasonable accommodation. All reasonable accommodation requests will be reviewed and evaluated on a case-by-case basis.

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