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Medical Device Development Jobs in Minneapolis, MN

The position offers opportunities for skill development through formal training and does not ... medical device assembly * High School Diploma, GED, or equivalent experience * Proficient in ...

This role is with a leading medical device manufacturing organization, is seeking Operators to join ... Comprehensive training and development programs Upon completion of waiting period associates are ...

New

Senior R&D Engineer

Minneapolis, MN · On-site

$109K - $149K/yr

We are currently hiring for a Senior R&D Engineer opportunity with one of our medical device clients in the greater Minneapolis area. This is a long-term onsite opportunity running through the end of ...

Working knowledge of clinical trial methodology, Good Clinical Practice (GCP), medical device development. Preferred Qualifications: * Demonstrated interest and commitment to transitioning from ...

Director of R&D - Medical Devices New Hope, MN Full-Time | $150,000-$200,000 + Bonus + Stock Options A leading medical device company in the Twin Cities is seeking a Director of Research ...

Medical Device Assembler/SS

Saint Paul, MN · On-site

$18.25 - $22.50/hr

... Medical Device Industry only; * must have some form of Assembly experience in MD; * Must be able to ... development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified ...

New

Senior R&D Engineer

Brooklyn Park, MN · On-site

$116 - $136/hr

We are seeking an experiencedResearch and Development Engineerwith deep medical device development expertise to participate in design activities across multiple structural heart programs. This role ...

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Showing results 1-20

Medical Device Development information

See Minneapolis, MN salary details

$30.3K

$55.8K

$84.5K

How much do medical device development jobs pay per year?

As of Sep 5, 2026, the average yearly pay for medical device development in Minneapolis, MN is $55,757.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,400.00 and $62,600.00 per year, depending on experience, location, and employer.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.

What are the key skills and qualifications needed to thrive in medical device development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is the difference between Medical Device Development vs Medical Device Quality Assurance?

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

Infographic showing various Medical Device Development job openings in Minneapolis, MN as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $55,757 per year, or $26.8 per hour.

Medical Device Toxicologist III

Boston Scientific

Arden Hills, MN • Hybrid

Full-time

Posted 8 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers


Job description

Additional Location(s): US-MN-Arden Hills; US-MA-Marlborough

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.           

About the role:

The Medical Device Toxicologist III at Boston Scientific provides technical support for toxicology and biocompatibility processes to meet global business objectives. This position contributes to the biological evaluation of medical device products, including toxicological risk assessments based on data from extractables and leachables studies, in support of new product development, sustaining activities and global regulatory submissions. The role applies established standards, procedures and risk-based approaches to help ensure patient safety and product quality while enabling timely product development and regulatory decisions.

Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.

Work model, sponsorship, relocation:

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.

Your responsibilities will include:

  • Support biocompatibility and toxicology processes initiated by department management and help ensure related information and data are accurate, reliable and aligned with Global Preclinical objectives and Quality Management System requirements.

  • Demonstrate a primary commitment to patient safety and product quality.

  • Author biocompatibility and chemical characterization test plans, biocompatibility assessments and reports, and assess test data and reports as assigned to support business objectives.

  • Author toxicological risk assessments as assigned to support divisional objectives, applying established procedures, precedents and scientific judgment.

  • Provide informal guidance to new or less-experienced team members on established biocompatibility and chemical characterization processes, as appropriate.

  • Maintain communication with internal customers on biocompatibility and toxicology topics and support the resolution of straightforward to moderately complex issues related to biological evaluation, chemical characterization and toxicological risk assessment.

  • Support biocompatibility, chemistry and toxicology testing strategies for assigned investigational and device development programs during technology and product development programs (TDP/PDP).

  • Apply working knowledge of regulatory requirements and internal procedures to support medical device submissions for assigned projects and divisions, with guidance on complex or unprecedented issues.

  • Participate, as assigned, in biocompatibility training for device development teams based on applicable standards, procedures and regulatory requirements.

  • Serve as a resource for factual biocompatibility and toxicology information for medical devices and pharmaceutical materials, which may include materials of animal origin, color additives, chemical exposure assessments and other chemical toxicities.

  • Apply established procedures, techniques, concepts and approaches to assigned biocompatibility and toxicology programs; identify issues and escalate complex or unprecedented matters as appropriate.

Qualifications:

Required qualifications:

  • Bachelor's degree in toxicology or a closely related field, such as biology, chemistry, biochemistry or biomedical engineering.

  • Minimum of 3 years' experience in a related field.

  • Knowledge of the biological evaluation of medical devices and/or drug-device combination products.

Preferred qualifications:

  • Master's degree in toxicology or a closely related field, such as biology, chemistry, biochemistry or biomedical engineering. Candidates with a master's degree and a minimum of 1 year's related experience will be considered.

  • Doctoral degree in toxicology or a related field, such as biology, chemistry, biochemistry or biomedical engineering.

  • Solid knowledge and practical application of toxicology principles and best practices.

  • Working knowledge of risk assessment methodologies, including the toxicological evaluation of medical device materials.

  • Working knowledge of regulatory standards and global regulatory requirements for medical devices and combination products.

  • Experience supporting GLP and non-GLP studies.

  • Excellent written and verbal communication skills.

  • Results-oriented and detail-oriented approach.

  • Ability to manage multiple assignments and priorities while meeting project timelines.

  • Ability to work effectively in a dynamic environment with a moderate level of guidance, independently on assigned work and collaboratively as part of a team.

Requisition ID: 633532 

Minimum Salary: $ 78300 

Maximum Salary: $ 148800 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status.  Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment.  Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.   As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.  


What Boston Scientific employees say

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About Boston Scientific

Sourced by ZipRecruiter

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.

Industry

Medical equipment and supplies manufacturing, manufacturing and construction

Company size

10,000+ Employees

Headquarters location

Marlborough, MA, US

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