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Quality Manager Medical Device Jobs in Minnesota

Actalent

Quality Manager

Saint Paul, MN

Quality Manager - Medical Technologies The Quality Manager for Medical Technologies plays a ... Experience working within regulated medical technology or medical device manufacturing environments ...

VOLT

Medical Device Assembler

Plymouth, MN · On-site

$17.50 - $19.25/hr

Complete documentation (paper & electronic) for traceability and quality control * Maintain ... Experience as a Medical Device Assembler or Production Assembler. * Strong attention to detail ...

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 ... Generate Quality System Records on applicable ACIST/BMT documentation as required * Perform timely ...

Bracco

Medical Device Assembler I

Eden Prairie, MN

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Generate Quality System Records on applicable ACIST/BMT documentation as required * Perform timely ...

Dynamic Group Inc

Quality Manager

Ramsey, MN · On-site

$85K - $115K/yr

Quality Management DIRECT REPORTS: Quality Inspectors SALARY: $85,000 - $115,000 (based on ... the medical device and related industries. With a commitment to excellence, innovation, and ...

VOLT

Medical Device Assembler - 1st Shift

Plymouth, MN · On-site

$18 - $18.75/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

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All JobsQuality Medical Device JobsQuality Manager Medical Device JobsQuality Manager Medical Device Jobs in Minnesota

Quality Manager Medical Device information

See Minnesota salary details

$23.5K

$84.4K

$154.7K

How much do quality manager medical device jobs pay per year?

As of Aug 24, 2026, the average yearly pay for quality manager medical device in Minnesota is $84,385.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,100.00 and $133,200.00 per year, depending on experience, location, and employer.

What does a quality manager do in the medical device industry?

A Quality Manager in the medical device industry is responsible for ensuring that products meet all regulatory requirements and quality standards throughout their lifecycle. They develop, implement, and monitor quality management systems, oversee internal and external audits, and work closely with manufacturing, engineering, and regulatory teams to maintain compliance with standards such as ISO 13485 and FDA regulations. Their role is critical to ensuring patient safety and product efficacy by preventing defects and ensuring consistent quality.

What are the key skills and qualifications needed to thrive as a quality manager in the medical device industry?

To thrive as a Quality Manager in the Medical Device industry, you need a solid background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and process improvement, often supported by a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), risk management tools (like FMEA), and certifications such as ASQ Certified Quality Auditor (CQA) or Six Sigma are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring cross-functional alignment. These skills and qualifications are crucial to ensure product safety, regulatory compliance, and the overall success of medical device manufacturing and delivery.

What are some common challenges quality managers face when ensuring compliance in the medical device industry?

Quality Managers in the medical device industry often encounter challenges such as keeping up with evolving regulatory requirements (like FDA, ISO 13485, and MDR), coordinating cross-functional teams to maintain strict quality standards, and managing documentation for audits. They must also address nonconformities quickly and implement corrective and preventive actions to avoid product recalls. Effective communication and strong attention to detail are essential for navigating these challenges while maintaining product safety and regulatory compliance.

What is the difference between Quality Manager Medical Device vs Quality Engineer Medical Device?

AspectQuality Manager Medical DeviceQuality Engineer Medical Device
Primary FocusOversees quality systems, compliance, and team managementDesigns, develops, and implements quality testing and inspection processes
CertificationsISO 13485, Six Sigma, Lead AuditorISO 13485, Six Sigma, Certified Quality Engineer (CQE)
Work EnvironmentManagement, regulatory compliance, cross-department collaborationProduct testing, process improvement, technical analysis
Industry UsageUsed across organizations to ensure overall quality managementUsed in product development and testing phases

The main difference is that the Quality Manager Medical Device focuses on managing quality systems and compliance at a strategic level, while the Quality Engineer Medical Device concentrates on technical testing and process improvements. Both roles require similar certifications and work within the same industry but serve different functions within quality assurance.

What are the most commonly searched types of Quality Medical Device jobs in Minnesota?

The most popular types of Quality Medical Device jobs in Minnesota are:

What are popular job titles related to Quality Manager Medical Device jobs in Minnesota?

For Quality Manager Medical Device jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Quality Manager Medical Device jobs in Minnesota look for?

The top searched job categories for Quality Manager Medical Device jobs in Minnesota are:

What cities in Minnesota are hiring for Quality Manager Medical Device jobs?

Cities in Minnesota with the most Quality Manager Medical Device job openings:

Quality Manager Medical Device jobs near you
Infographic showing various Quality Manager Medical Device job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 15% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $84,385 per year, or $40.6 per hour.

Quality Manager - Medical Device

Chanhassen, MN • On-site

PMT Corporation
See more jobs at PMT Corporationexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 6 days ago

Job description

Located in Chanhassen, Minnesota, PMT Corporation was established in 1979 as a private company dedicated to the research and development of specialty products, devices and instruments used in the medical field. PMT Corporation is known for manufacturing and distributing high end, innovative products within the orthopedic, neurosurgery and plastic surgery markets.

DESCRIPTION:

PMT is hiring a Quality Manager to develop and implement quality practices where necessary. To enforce company’s compliance to the GMPs, ISO requirements and other requirements necessary of a medical device manufacture of safe and effective devices. To assist and train employees where necessary on the GMPs and to follow the established system. To apply good technical solutions and to ensure empirical evidence is documented per written procedures.

RESPONSIBILITIES include but not limited to:

  • Becomes personally skilled in all inspection and testing procedures.
  • Coordinates and conducts quality audits per the defined schedule.
  • Develops procedures and SOPs to control inspected and non-inspected product.
  • Assists in the development, maintenance and implementation of processes and procedures in accordance with regulatory requirements.
  • Implements procedures and SOPs for QA/QC and ISO audits of Receiving, Receiving Inspection, Inventory, Manufacturing, manufacturing test, In-process inspection, Final inspection, engineering, Pre-production, new product development, Customer Service, Training, Purchasing, Shipping, and Documentation as well as other departments that effect quality, GMPs and other regulatory requirements.
  • Monitors, maintains and assists with validation, sterilization, risk management and design activities.
  • Establishes that all manufacturing processes and procedures are in accordance with properly released documentation.
  • To assist in the resolution, documentation, customer responses of product complaints.
  • Coordinate efforts for external services (i.e. calibration, environmental testing, and standards) to perform tasks according to documented schedules.
  • Coordinate and assist in corrective and preventative action activities and solutions
  • Monitor and trend quality indicators to report to management and to provide early warning for quality related issuesall employees throughout all departments
  • Work with cross-functional teams to complete all assigned tasks

REQUIREMENTS

  • Bachelor’s degree in related field of engineering, science, or regulatory affairs, or equivalent experience.
  • Strong attention to detail.
  • Minimum 5 years’ experience in medical device industry.
  • Experience working with quality system, ISO and quality assurance.
  • Excellent communication and time management skills.
  • Proficient in Microsoft Office Suite.

Location: Chanhassen, MN

PMT is an Equal Opportunity Employer

Company Description

PMT Corporation, established in 1979, is dedicated to the research and development of specialty products, devices and instruments used in the medical field including, but not exclusive to, Plastic and Reconstructive Surgery, Neurosurgery, Orthopedic Spine medicine and Gastrointestinal Endoscopy.

Please visit us at www.pmtcorp.com.

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