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Biotech Quality Control Jobs in Minnesota (NOW HIRING)

Quality Control Technician

Minneapolis, MN

$19.50 - $25/hr

The Quality Control Technician works hands-on with porcine tissues, prepares and processes ... Interest in working in a biotech environment with opportunities for advancement to Technician II ...

Apply Early

Quality Manager

Glencoe, MN · On-site

$90K - $105K/yr

... control processes to meet customer expectations. Monitor and evaluate the performance of the ... Cook Biotech in IN. and Collagen Solutions, MN. Our new brand identity emphasizes our unique ...

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... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... Deep working knowledge of quality assurance, quality control, process validation, design quality ...

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... Deep working knowledge of quality assurance, quality control, process validation, design quality ...

R&D Scientist

Saint Cloud, MN · On-site

$86K - $107K/yr

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 ...

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 ...

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Showing results 1-20

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 Jul 6, 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.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

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.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

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 are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

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 does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency 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:
Quality Control Technician

Quality Control Technician

Actalent

Minneapolis, MN

$19.50 - $25/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago

Be an early applicant


Job description

Job Title: Quality Control Technician
Job Description

This role focuses on supporting the production of biological medical devices derived from porcine liver in a regulated cleanroom manufacturing environment. The Quality Control Technician works hands-on with porcine tissues, prepares and processes materials according to strict procedures, and helps maintain a sterile and compliant workspace. The position offers consistent full-time hours with some overtime, opportunities for advancement to higher technician levels, and the chance to contribute to innovative biotech products within a small, collaborative team.

Responsibilities

  • Work in a cleanroom manufacturing environment to support the creation of biological medical devices derived from porcine liver.
  • Receive porcine livers and verify that incoming materials meet established requirements and documentation standards.
  • Trim porcine livers and prepare tissue samples according to defined specifications and standard operating procedures (SOPs).
  • Scoop, measure, and mix chemical solutions for use with porcine livers, following aseptic and sterile processing techniques.
  • Perform decellularization of porcine livers using established protocols, ensuring consistency and quality in processed tissues.
  • Create, cut, and prepare specific tissue pieces for use in medical devices, maintaining accuracy and attention to detail.
  • Sterilize the cleanroom environment and equipment in accordance with SOPs and good manufacturing practice (GMP) requirements.
  • Follow all SOPs and GMP guidelines to ensure compliance with regulatory and quality standards throughout the production process.
  • Work in the cleanroom during non-build weeks to support assembly activities and related production tasks.
  • Assemble components and materials as needed to support device production and quality control activities.
  • Sweep floors, clean work areas, and perform general housekeeping tasks to maintain a safe, organized, and sterile environment.
  • Update manufacturing records (MFR) and other documentation accurately and in a timely manner to reflect production activities.
  • Support administrative tasks, including order receiving, shipping, and related paperwork, as needed.
  • Assist with sterile processing and sterilization of equipment, materials, and workspaces.
  • Apply aseptic technique consistently when handling tissues, solutions, and equipment.
  • Collaborate with a small team of technicians and partner with the research and development (R&D) team on production and process-related tasks.
  • Work directly with porcine livers during production and assist R&D with porcine kidneys and other tissues during downtime.
  • Stand for extended periods and safely lift bins and livers weighing approximately 5–15 pounds throughout the workday.
  • Adhere to production timelines, ensuring that products move from start to finish according to the established Monday-to-following-Tuesday schedule.
  • Participate in build weeks and non-build weeks, adapting to varying start times, workloads, and mandatory overtime as required.
Essential Skills
  • At least 6 months of experience working within a cleanroom setting.
  • Associate degree in a medical or science field.
  • Experience following SOPs in a GMP (Good Manufacturing Practice) environment.
  • Demonstrated strong attention to detail, including accurate documentation and adherence to procedures.
  • Hands-on experience with cleanroom practices and protocols.
  • Ability to perform sterile processing and apply aseptic technique when handling tissues and solutions.
  • Experience with chemical mixing in a controlled or regulated environment.
  • Ability to perform tissue trimming and handling of biological samples.
  • Knowledge of basic biology concepts relevant to working with animal tissues.
  • Capability to stand for most of the workday and safely lift 5–15 pound bins and livers.
  • Comfort working in a regulated environment with defined timelines and quality standards.
Additional Skills & Qualifications
  • Associate degree in a scientific field such as biology is preferred.
  • Experience in a laboratory setting working with porcine or other animal tissue is highly beneficial.
  • Background in roles such as butcher, barista, quality technician in the food industry, landscaping, or similar hands-on positions, especially when combined with an outdated or prior scientific degree.
  • Familiarity with cleanroom operations, tissue samples, sterile processing, and aseptic techniques.
  • Experience with chemical handling, chemical mixing, and sterilization processes.
  • Ability to follow detailed SOPs and manufacturing records with high accuracy.
  • Interest in working in a biotech environment with opportunities for advancement to Technician II and Technician III levels.
  • Comfort working independently within a smaller team while maintaining strong communication with colleagues and R&D staff.
Work Environment

The role is based in a new biotech facility with a cleanroom that is being built out and expanded. The team will initially consist of three technicians who work closely with the research and development (R&D) team. The position involves direct, hands-on work with porcine livers during production and support for R&D activities, including work with porcine kidneys, during downtime. The environment is regulated and follows GMP standards, with a focus on sterile processing, aseptic technique, and strict adherence to SOPs. Production runs on a defined timeline, with products moving from start on Monday to shipment the following Tuesday. Work hours are structured around build and non-build weeks. Non-build weeks typically run Monday through Friday from 8:00 a.m. to 4:30 p.m., totaling around 36 hours per week. Build weeks generally require 40+ hours, with some mandatory overtime (approximately 42–44 hours). During build weeks, Monday hours are 8:00 a.m. to 4:30 p.m.; Tuesday through Thursday shifts start between 6:00–6:30 a.m. and end around 4:30–5:00 p.m.; Friday shifts usually start at 7:00 a.m. and end when production is complete, often around 1:00–2:00 p.m. The work requires standing for most of the day and lifting 5–15 pound bins and livers. The dress code aligns with cleanroom and sterile environment requirements, including appropriate protective clothing and adherence to all cleanliness and safety protocols.

Job Type & Location

This is a Contract to Hire position based out of plymouth, MN.

Pay and Benefits

The pay range for this position is $21.00 - $21.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in plymouth,MN.

Application Deadline

This position is anticipated to close on Jul 9, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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