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Biocompatibility Jobs in Maple Grove, MN (NOW HIRING)

Actalent

Design Engineer II

Minneapolis, MN

Knowledge of FDA Quality System Regulation and relevant ISO standards, including usability, sterilization, biocompatibility, and regulatory submission support. * Experience designing plastic ...

NAMSA

Supervisor, Sample Preparation

Minneapolis, MN

$68K - $133K/yr

Trains technicians in sample preparation, formulation, and extraction of prepared samples in support of in vitro and in vivo biocompatibility assays, pharmacology and toxicology procedures. Also ...

Evergen

Sr. R&D Engineer

Eden Prairie, MN · On-site

$100K - $130K/yr

Identify and lead interactions with external vendors such as test labs (e.g. biocompatibility, animal study, and analytical) and suppliers. * Independently author engineering reports and ...

rms Company

Chemical Process Technician

Coon Rapids, MN · On-site

$21.20 - $30.72/hr

Lab Technician/Biocompatibility Technician Preferred Knowledge, Skills and Abilities * Experience with process validation. * Knowledge of Hazardous Chemical Handling. * Knowledge of testing methods ...

rms Company

Chemical Process Technician

Coon Rapids, MN · On-site

$21.20 - $30.72/hr

Lab Technician/Biocompatibility Technician Preferred Knowledge, Skills and Abilities * Experience with process validation. * Knowledge of Hazardous Chemical Handling. * Knowledge of testing methods ...

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Biocompatibility information

See Maple Grove, MN salary details

$42K

$118.1K

$219.1K

How much do biocompatibility jobs pay per year?

As of Sep 4, 2026, the average yearly pay for biocompatibility in Maple Grove, MN is $118,132.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,000.00 and $138,700.00 per year, depending on experience, location, and employer.

What is a biocompatibility job?

A Biocompatibility job involves evaluating medical devices, materials, and implants to ensure they are safe and non-toxic for human use. Professionals in this role analyze the interactions between biomaterials and biological systems, conducting risk assessments and regulatory compliance reviews. They work closely with engineers, scientists, and regulatory teams to meet standards like ISO 10993. This job is critical in ensuring patient safety and securing product approvals for medical devices.

What are the typical daily responsibilities in biocompatibility?

Professionals in Biocompatibility routinely assess the biological safety of new materials or devices, design or coordinate laboratory tests, and analyze results to determine compliance with regulatory standards. Their day-to-day work often involves preparing technical reports, collaborating with R&D and regulatory teams, and communicating findings to project stakeholders. You may also contribute to risk assessments, provide input during product development stages, and stay updated on evolving international regulations. This role requires balancing technical expertise with proactive communication to ensure the safe and timely approval of medical products.

What are the key skills and qualifications needed for biocompatibility?

To thrive in a Biocompatibility role, you typically need a background in biomedical engineering, materials science, or a related life science field, with strong knowledge of biological safety and regulatory requirements for medical devices. Familiarity with ISO 10993 standards, biocompatibility testing methods, and data analysis tools is essential, along with potential certification in regulatory affairs or toxicology. Attention to detail, effective communication, and problem-solving abilities are vital soft skills for collaborating across multidisciplinary teams. These skills ensure accurate safety evaluations and regulatory compliance, which are crucial for bringing safe and effective medical products to market.

What job categories do people searching Biocompatibility jobs in Maple Grove, MN look for?

The top searched job categories for Biocompatibility jobs in Maple Grove, MN are:

What cities near Maple Grove, MN are hiring for Biocompatibility jobs?

Cities near Maple Grove, MN with the most Biocompatibility job openings:

Biocompatibility jobs near you
Infographic showing various Biocompatibility job openings in Maple Grove, MN as of August 2026, with employment types broken down into 72% Full Time, and 28% Contract. Highlights an 100% In-person job distribution, with an average salary of $118,132 per year, or $56.8 per hour.

Lab Tech (NAMSA Talent Building Community)

NAMSA

Minneapolis, MN

$14.81/hr

Full-time

Re-posted 3 days ago

Key responsibilities

  • Conduct sample preparation for in vivo and in vitro biocompatibility, pharmacology, and toxicology studies according to study protocols.

  • Operate, maintain, and monitor laboratory equipment such as incubators, autoclaves, hoods, and sterilizers, ensuring proper functioning and cleanliness.

  • Review incoming test articles and paperwork for accuracy, maintain lab supplies, and document test article tracking and study data.

NAMSA rating

8.3

Company rating: 8.3 out of 10

Based on 16 frontline employees who took The Breakroom Quiz

37th of 121 rated laboratories

Job description

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.

We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry's premier provider. We provide support for clients during every step of the product development lifecycle and beyond.

Come and work for an organization with the:

Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the

Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core

Values:

  • Act with integrity in everything we do.
  • Provide best-in-class customer experiences.
  • Develop superior talent and deliver expertise.
  • Respond with agility and provide timely results.
  • Embrace collaboration, diverse perspectives and ideas.

Job Description:

Strictly adheres to GLP guidelines (good documentation, labeling and expiration of materials, participation in audits).
Conducts sample preparation for Sponsor materials as directed by study protocols for in vivo and in vitro biocompatibility assays, pharmacology studies, and toxicology studies.
Performs the extraction process on prepared samples in accordance with ISO, USP and JMHLW regulations as directed by study protocols for biocompatibility assays.
May prepare and maintain sterile glassware for the In-vitro lab and sample preparation process. Processes glassware through washer, autoclave and depyrogenation oven as needed.
Operates, cleans and maintains incubators, autoclaves, hoods, and other equipment routinely utilized.
Performs preparation of media/reagents, maintains reagents and/or test article as required for testing, and maintains lab supplies/inventory.
Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and taking all concerns to management or Study Directors as required.
Maintains an efficient and clean work area by organizing and restocking the sample preparation lab as needed.
Communicates with external clients in regards to particulate observations or article abnormality. Routinely communicates with Study Directors, Quality Assurance and NAMSA Associates about issues, results, or audits.
Responsible for daily monitoring of laboratory equipment, being on-call and responding to continuous monitoring alarms. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures.
Performs ethylene oxide processing of study-related materials through the in-house sterilizer.
Adheres to established company processes.
Completes chain of custody documentation for test article tracking.
Responsible for performing routine equipment microbiological monitoring.
Maintains ancillary records (logbooks, worksheets).
Communicates test schedule updates to NAMSA Associates or management as needed.
Responsible for the assessment and completion of GLP study article data retention/archival.
May assist in receipt and release of lab supplies and inventory.
May assist trainers or may become a certified trainer to provide Associates with on the job training for basic lab tasks and media preparation.
Other duties as assigned.

Qualifications & Technical Competencies:

Experience in a GLP laboratory setting preferred.
Basic mathematical knowledge is essential for surface area/volume ratio calculations that are part of the sample preparation process.
An Associate or Bachelor degree in related scientific field is required. Individuals with sufficient relevant work experience may be considered at the discretion of management.

** Future openings at NAMSA (Talent Building Community)

Working Conditions:

While performing the duties of this job, the Associate is occasionally exposed to sharps and hazardous or caustic chemicals. The noise level in the work environment is usually moderate. Eye protection is required in designated areas and when performing specific tasks. The Associate is occasionally exposed to small laboratory animals and may, on rare occasions, be exposed to blood borne pathogens and zoonotic diseases.
While performing the duties of this job, the Associate is regularly required to stand; walk; reach with hands and arms; use hands to finger, handle, or feel objects, tools, or controls; talk; and hear. The Associate is occasionally required to sit, climb, balance, stoop, kneel, crouch, or crawl. The Associate must occasionally lift and/or move up to 50 pounds. The Associate may be required to view computer monitors and stand for extended periods of time.

Pay Range Minimum:

$14.81

Pay Range Target:

$20.00

Pay Frequency:

Hourly

Please Note: Individual base pay depends on various factors, in addition to primary work location, such as complexity and responsibility of role, job duties/requirements, and relevant experience and skills.

NAMSA is an equal employment opportunity company. NAMSA participates in pre-employment background and drug screen processes aligned to local, state and federal laws.

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