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General Manager Medical Device Jobs in Minnesota

ATR International

Medical Device Assembler

Plymouth, MN · On-site

$18.58/hr

... related medical device assemblies. Performs routine assignments according to specified and/or ... Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals ...

Techlink Systems

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Medical Device Assembler (MM25)

Saint Paul, MN · On-site

$18 - $18.75/hr

... Medical Device Industry only * Must have some form of Assembly experience in medical devices ... We serve the contract staffing, direct hire, staff augmentation, recruitment, HR management, and ...

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The Dolphin Group

Medical Assembler

Minneapolis, MN · On-site

$18 - $21/hr

Perform general assembly and secondary production operations * Requirements * Aminimum of 6 monthsof medical device assemblyandmicroscope experience * Ability to read and understand work instructions ...

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General Manager Medical Device information

See Minnesota salary details

$29.4K

$63.7K

$107.7K

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

As of Aug 28, 2026, the average yearly pay for general manager medical device in Minnesota is $63,687.00, according to ZipRecruiter salary data. Most workers in this role earn between $48,500.00 and $72,500.00 per year, depending on experience, location, and employer.

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

A General Manager in the medical device industry oversees the overall operations, strategy, and profitability of a medical device company or division. They are responsible for managing teams, ensuring regulatory compliance, developing business plans, and driving growth through sales and innovation. General Managers work closely with product development, marketing, and regulatory affairs to ensure products meet quality standards and market needs. They also manage budgets, stakeholder relationships, and ensure the organization adheres to industry regulations.

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

To thrive as a General Manager in the medical device sector, you need strong leadership, business acumen, regulatory knowledge, and typically a degree in business, engineering, or life sciences. Familiarity with quality management systems (QMS), FDA and ISO regulations, and experience with CRM and ERP software are essential. Exceptional communication, strategic thinking, and problem-solving skills help drive organizational growth and foster cross-functional team collaboration. These skills and qualifications are crucial for ensuring regulatory compliance, operational efficiency, and sustained business success in a competitive and highly regulated market.

What are some common challenges faced by a general manager in the medical device industry, and how can they be effectively addressed?

General Managers in the medical device sector often encounter challenges related to navigating regulatory requirements, managing cross-functional teams, and ensuring product innovation while meeting market needs. Balancing compliance with FDA and international standards, coordinating between R&D, manufacturing, and sales, and responding quickly to technological advancements are crucial aspects of the role. Effective communication, continuous learning about regulatory changes, and fostering a collaborative team culture can help address these challenges and drive organizational success.

What is the difference between General Manager Medical Device vs Product Manager Medical Device?

AspectGeneral Manager Medical DeviceProduct Manager Medical Device
CredentialsTypically requires advanced degrees (e.g., MBA, engineering), industry certificationsRequires relevant technical or business degrees, certifications often preferred
Work EnvironmentExecutive leadership, strategic planning, cross-departmental oversightProduct development, marketing, customer engagement, project management
Employer & Industry UsageUsed in medical device manufacturing companies, healthcare organizationsCommon in medical device companies, focusing on product lifecycle
Search & Comparison IntentUnderstanding leadership roles, strategic responsibilitiesFocus on product development, market strategy

The main difference is that the General Manager Medical Device oversees overall company operations and strategic direction, while the Product Manager Medical Device focuses on managing specific medical device products throughout their lifecycle. The General Manager has broader responsibilities, including business growth and compliance, whereas the Product Manager concentrates on product success and market fit.

What is the role of a general manager medical device?

A General Manager in the medical device industry oversees the overall operations, strategic planning, and business development of a medical device company or division. They coordinate cross-functional teams, ensure regulatory compliance, and drive product innovation to meet market needs, often requiring leadership skills and industry-specific certifications. The role involves managing budgets, sales, and marketing efforts to achieve company goals.

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

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

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

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

General Manager Medical Device jobs near you
Infographic showing various General 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 $63,687 per year, or $30.6 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 10 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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