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Quality Control Biotechnology 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 ...

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

$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

$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 ...

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 ...

Danaher

Sr. Quality Engineer

New Brighton, MN · On-site

$115K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... Lead value stream specific quality tasks, including change control, training, non-conformance, and ...

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 Seeds

Production Technician

Cokato, MN · On-site

  • 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 · On-site

  • 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 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

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) ...

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Showing results 21-40

All JobsQuality Control Biotechnology JobsQuality Control Biotechnology Jobs in Minnesota

Quality Control Biotechnology information

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How much do quality control biotechnology jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for quality control biotechnology in Minnesota is $20.54, according to ZipRecruiter salary data. Most workers in this role earn between $17.64 and $22.60 per hour, depending on experience, location, and employer.

What is a quality control biotechnology job?

Quality Control Biotechnology jobs involve ensuring that biotechnological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet required quality and safety standards. Professionals in this field design and perform tests, analyze data, and document results to verify that products comply with regulatory guidelines. They often work in laboratories, using specialized equipment to detect contaminants or inconsistencies. These roles are crucial for maintaining product integrity and protecting public health.

What are the key skills and qualifications needed to thrive as a quality control biotechnology professional?

To thrive as a Quality Control professional in Biotechnology, you need a solid background in biology or chemistry, attention to detail, and knowledge of regulatory standards, often supported by a relevant degree. Familiarity with laboratory equipment, analytical techniques (like HPLC, PCR), and quality management systems such as GMP or ISO 9001 is typically required. Strong problem-solving skills, teamwork, and clear communication help you excel in ensuring product integrity and compliance. These skills are crucial for maintaining high product standards, meeting regulatory requirements, and ensuring the safety and efficacy of biotechnological products.

What are typical challenges faced by professionals in quality control biotechnology, and how can they be addressed?

Professionals in Quality Control Biotechnology often encounter challenges such as maintaining compliance with stringent regulatory standards, managing tight deadlines for product release, and adapting to rapidly evolving technologies. To address these issues, staying updated on regulatory changes, implementing robust documentation practices, and participating in ongoing training are essential. Collaboration with cross-functional teams, such as Research & Development and Manufacturing, also helps ensure that quality standards are integrated throughout the production process.

What is the difference between Quality Control Biotechnology vs Quality Assurance Biotechnology?

AspectQuality Control BiotechnologyQuality Assurance Biotechnology
Primary FocusTesting and inspecting biotech products to ensure they meet standardsDeveloping and implementing processes to prevent defects and ensure quality
Work EnvironmentLaboratories, testing facilitiesOffice settings, compliance departments
CertificationsGMP, GLP, laboratory certificationsGMP, ISO, audit-related certifications

While both roles aim to ensure biotech product quality, Quality Control Biotechnology focuses on testing and inspection, whereas Quality Assurance Biotechnology emphasizes process development and compliance to prevent issues. Both are essential for product integrity in the biotech industry.

How to become a quality control biotechnology specialist?

To become a quality control biotechnology specialist, candidates typically need a bachelor's degree in biotechnology, biology, or a related field. Gaining experience with laboratory techniques, quality assurance protocols, and regulatory standards such as GMP or ISO is important, and certifications like ASQ's Certified Quality Auditor can enhance prospects. Strong attention to detail, analytical skills, and familiarity with laboratory equipment are also essential for success in this role.

What does quality control biotechnology do in biotech?

Quality Control Biotechnology professionals are responsible for testing and analyzing biological products to ensure they meet safety, quality, and regulatory standards. They perform assays, validate processes, and document results using laboratory instruments and techniques, often working under Good Manufacturing Practice (GMP) guidelines. Their work helps ensure the integrity and compliance of biotech products before they reach the market.

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

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

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

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

Quality Control Biotechnology jobs near you
Infographic showing various Quality Control Biotechnology job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 4% Contract, and 2% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $42,714 per year, or $20.5 per hour.

Quality Manager ISO9001

Harvard Bioscience

Saint Paul, MN • On-site

$110K - $160K/yr

Full-time

Posted 24 days ago

Job description

ABOUT HARVARD BIOSCIENCEHarvard 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 RESPONSIBILITIESLeadership: 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 REQUIREDStrong 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 EQUIVALENT4-year engineering degree with 5+ years relevant experience and 2+ years of management experience preferred. AN EQUAL EMPLOYMENT OPPORTUNITY EMPLOYER/VETERAN/DISABILITYFLSA: ExemptADA DISCLAIMERIn 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.
Job Posted by ApplicantPro