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Medical Device Manufacturing Jobs in Minnesota (NOW HIRING)

rms Company

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CNC Machinist / Medical Device Manufacturing

Anoka, MN · On-site

$21.20 - $40.67/hr

CNC Machinist - Medical Device Manufacturing Build Parts That Improve Lives Are you a CNC Machinist who takes pride in producing precision parts and solving machining challenges? At rms Company, you ...

Three Point Solutions

Medical Assembler

Brooklyn Park, MN · On-site

$19 - $20.80/hr

Medical Device Manufacturing Company Duration: 1 Year Location: Brooklyn Park, MN 55445 Shift: 1st Shift (5:00 AM - 3:30 PM) Key Responsibilities: * Assemble medical devices on multiple product lines.

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Demonstrated ability to follow documented manufacturing processes (i.e. written work instructions ...

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Demonstrated ability to follow documented manufacturing processes (i.e. written work instructions ...

Three Point Solutions

Medical Assembler

Brooklyn Park, MN

$18.75 - $23/hr

Medical Device Manufacturing Company Duration: 1 Year Location: Brooklyn Park, MN 55445 Shift: 1st Shift (5:00 AM - 3:30 PM) Key Responsibilities: * Assemble medical devices on multiple product lines.

Three Point Solutions

Medical Assembler

Brooklyn Park, MN

$18.75 - $23/hr

Medical Device Manufacturing Company Duration: 1 Year Location: Brooklyn Park, MN 55445 Shift: 1st Shift (5:00 AM - 3:30 PM) Key Responsibilities: * Assemble medical devices on multiple product lines.

Collaborative LLC

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Assembler 2nd shift

Plymouth, MN · On-site

$20/hr

The ideal candidate has previous medical device manufacturing experience, excellent hand dexterity, strong attention to detail, and the ability to work accurately while following detailed procedures ...

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Medical Device Manufacturing information

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How much do medical device manufacturing jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for medical device manufacturing in Minnesota is $26.56, according to ZipRecruiter salary data. Most workers in this role earn between $22.60 and $31.06 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in medical device manufacturing?

To thrive in Medical Device Manufacturing, you need strong attention to detail, knowledge of quality assurance processes, and an understanding of regulatory standards such as ISO 13485 or FDA requirements. Experience with manufacturing equipment, ERP systems, and specialized tools for assembly and testing is typically required, and certification in areas like Six Sigma or Lean Manufacturing can be advantageous. Effective communication, teamwork, and problem-solving skills help individuals excel in fast-paced, multidisciplinary environments. These skills are vital for maintaining product safety, ensuring regulatory compliance, and meeting production targets in the highly regulated medical device industry.

Is medical device manufacturing a good job?

Medical device manufacturing is considered a stable and growing field with opportunities for skilled workers, including roles in assembly, quality control, and engineering. It often requires attention to detail, technical skills, and adherence to safety and regulatory standards, with potential for career advancement and competitive wages.

What career advancement opportunities are available in medical device manufacturing?

Medical Device Manufacturing offers a variety of career advancement paths, allowing employees to move into roles such as production supervisor, quality assurance specialist, or process engineer as they gain experience. Many companies provide on-the-job training, mentorship programs, and support for additional certifications to help employees further develop their technical and leadership skills. Team members who demonstrate strong performance and a commitment to continuous improvement may also transition into management positions or cross-functional roles in research and development, regulatory affairs, or supply chain management. This field values both specialized technical expertise and a proactive approach to professional growth, providing long-term career stability and diverse opportunities.

What is a medical device manufacturing job?

A Medical Device Manufacturing job involves producing, assembling, and testing medical devices to ensure they meet regulatory and quality standards. Workers in this field may operate machinery, inspect products, and follow strict guidelines to maintain safety and efficiency. Roles can range from machine operators and quality control inspectors to engineers and regulatory compliance specialists. This industry is essential for creating devices like surgical instruments, pacemakers, and diagnostic equipment used in healthcare. Attention to detail, adherence to regulations, and technical skills are key for success in this field.

What job categories do people searching Medical Device Manufacturing jobs in Minnesota look for? The top searched job categories for Medical Device Manufacturing jobs in Minnesota are:
What cities in Minnesota are hiring for Medical Device Manufacturing jobs? Cities in Minnesota with the most Medical Device Manufacturing job openings:
Medical Device Manufacturing jobs near you
Infographic showing various Medical Device Manufacturing job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $55,250 per year, or $26.6 per hour.

Engineer II - Med Device / Manufacturing Engineer

FLEX Vascular

Plymouth, MN • On-site

$77K - $99K/yr

Full-time

Posted 14 hours ago

Posted today

Job description

ENGINEER II - Medical Device Product Development & Manufacturing Engineering (Vascular Access Devices)

Position Summary

The Engineer II role supports the design, development, validation, and sustaining engineering of vascular access devices and their associated manufacturing processes. Working within established procedures and under general supervision, the Engineer role II independently executes defined engineering projects including test method development, process and equipment qualification, fixture design, and technical investigations and documents the results in compliance with the Quality Management System and applicable regulatory requirements. The role escalates novel or ambiguous technical problems to senior engineering staff and contributes to cross-functional design and process review activities.

Essential Duties and Responsibilities

Design and Development Support

Provide project support including device and component testing, protocol authoring, documentation of test results, data analysis, and preparation of technical reports in accordance with design control procedures.

Contribute to Design History File (DHF) and Device Master Record (DMR) content for assigned projects.

Design, model, and fabricate test and manufacturing fixtures, including CAD modeling and additive manufacturing (3D printing) of prototypes.

Participate actively in design and process reviews.

Test Method and Process Validation

Design and execute test method validations (TMV), measurement systems analysis (MSA) including Gage R&R studies, and designs of experiments (DOE); analyze and report results.

Support line validation and qualification activities including IQ, OQ, and PQ authoring protocols and reports and executing testing.

Develop and document statistical rationale for sampling plans, sample sizes, acceptance criteria, and confidence/reliability targets.

Risk Management and Quality Systems

Participate in risk management activities including PFMEA, DFMEA, and use-related FMEA (uFMEA), and contribute to the risk management file in accordance with ISO 14971.

Perform process mapping and support process characterization and improvement initiatives.

Author and assess engineering change orders (ECOs) and change control records, including impact and validation assessments.

Provide technical investigation support for nonconformances, CAPAs, and complaint investigations. Complaint reportability and regulatory decisions remain the responsibility of Quality Assurance and Regulatory Affairs.

Manufacturing and Supplier Support

Interact with suppliers and vendors to facilitate new manufacturing processes or changes to existing processes, including technical support during process transfers.

Perform product and component inspections in compliance with company policies and procedures.

Support shipping and receiving of commercial product and components as required.

Qualifications

Required

Bachelor's degree in Mechanical, Biomedical, Manufacturing, or a related engineering discipline.

2-5 years of engineering experience, preferably in medical device or another FDA-regulated manufacturing environment.

Working knowledge of design controls and validation principles (IQ/OQ/PQ, TMV, MSA).

Demonstrated ability to author clear technical protocols and reports suitable for a regulated document system.

Proficiency with 3D CAD software (e.g., SolidWorks) and standard office productivity tools.

Preferred

Familiarity with medical device standards and guidance documents.

Experience with statistical software (e.g., Minitab, JMP) and applied statistical methods.

Experience with GD&T and inspection method development.

Experience with catheter, guidewire, or other vascular access device manufacturing processes.

Experience working in an ISO Class 7/8 controlled environment.