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Manager Medical Device Operations Jobs in Minnesota

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 ... Standard Operation Procedures (SOP), Work Instructions (WI), Engineering Prints and Bills of ...

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 ... Standard Operation Procedures (SOP), Work Instructions (WI), Engineering Prints and Bills of ...

Aerotek

Medical Assembler

Hopkins, MN

$20 - $26/hr

Medical Assembler This role focuses on assembling implantable medical devices used to treat rotator ... device operation. The environment offers variety in daily tasks, allowing you to learn many ...

Actalent

Medical Device Scientist

Maple Grove, MN

$31 - $36/hr

... and operational qualification (IQ/OQ) protocols. * Adhere to all environmental health and safety ... Effectively manage multiple projects and priorities in a timeline-driven environment, ensuring ...

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Manager Medical Device Operations information

What are Manager Medical Device Operations?

A Manager Medical Device Operations oversees the daily activities and processes involved in manufacturing, distributing, and maintaining medical devices. They ensure that operations comply with regulatory standards, manage teams, and work to optimize efficiency, quality, and safety. This role often involves coordinating with other departments, handling audits, and implementing process improvements to meet organizational goals. They play a critical role in ensuring that medical devices reach healthcare providers and patients safely and on time.

What are some common challenges faced by a Manager in Medical Device Operations, and how can they be addressed?

Managers in Medical Device Operations often face challenges such as ensuring compliance with strict regulatory standards, coordinating cross-functional teams, and managing supply chain complexities. Staying proactive with regulatory updates, fostering open communication among departments, and implementing robust quality management systems can help address these issues. Additionally, investing in staff training and process improvement initiatives can streamline operations and minimize delays or compliance risks.

What are the key skills and qualifications needed to thrive as a Manager Medical Device Operations, and why are they important?

To excel as a Manager Medical Device Operations, you need expertise in supply chain management, regulatory compliance (such as FDA and ISO standards), and operational leadership, typically supported by a bachelor’s degree in engineering, life sciences, or business. Familiarity with ERP systems, quality management software, and relevant certifications like Six Sigma or PMP are commonly required. Strong communication, problem-solving, and team leadership skills help drive cross-functional collaboration and continuous improvement. These competencies are essential for ensuring product quality, regulatory adherence, and efficient operations in a highly regulated industry.
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Manager Medical Device Operations jobs near you
Infographic showing various Manager Medical Device Operations job openings in Minnesota as of July 2026, with employment types broken down into 74% Full Time, 18% Part Time, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.
Quality Manager - Medical Device

Quality Manager - Medical Device

PMT Corporation

Chanhassen, MN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

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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