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Contract Manager Medical Device Jobs in Minnesota

VOLT

Medical Device Assembler

Plymouth, MN · On-site

$17.50 - $19.25/hr

... is a full time, contract opportunity. Schedule: 1st Shift : 5:00 AM - 3:30 PM Monday through ... Experience as a Medical Device Assembler or Production Assembler. * Strong attention to detail ...

VOLT

Medical Device Assembler

Saint Paul, MN · On-site

$17.50 - $18.75/hr

... contract opportunity. Schedule: 1st Shift: Monday - Thursday, 6:00 AM to 4:30 PM The ideal ... Previous Medical Device Assembly experience required * High school diploma or GED required * Prior ...

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 ...

VOLT

Medical Device Assembler - 1st Shift

Plymouth, MN · On-site

$18 - $18.75/hr

This is a full time, contract opportunity. Schedule: 1st Shift: 5:00 AM to 3:30 PM (Monday through ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

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Contract Manager Medical Device information

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

A Contract Manager in the medical device industry is responsible for overseeing the drafting, negotiation, and administration of contracts related to the development, manufacturing, and distribution of medical devices. They ensure that all agreements comply with regulatory requirements, company policies, and industry standards. Their role helps safeguard the company’s interests while fostering strong relationships with suppliers, customers, and regulatory agencies. Additionally, they work closely with legal, sales, and compliance teams to mitigate risks and resolve contractual issues.

What are some common challenges a contract manager faces when working with medical device agreements?

Contract Managers in the medical device industry often navigate complex regulatory requirements while ensuring contracts align with both business objectives and compliance standards. Challenges may include negotiating terms that adhere to FDA regulations, managing intellectual property clauses, and coordinating among legal, sales, and regulatory teams. Success in this role often relies on strong attention to detail and the ability to balance multiple stakeholders’ interests. Staying updated on evolving industry standards can also be demanding but is crucial for effective contract management.

What are the key skills and qualifications needed to thrive as a contract manager in the medical device industry, and why are they important?

To excel as a Contract Manager in the Medical Device industry, you need expertise in contract law, negotiation, and regulatory compliance, often supported by a bachelor’s degree in business, law, or a related field. Familiarity with contract management software (such as Icertis or SAP Ariba), e-signature platforms, and knowledge of FDA or EU MDR regulations are typically required. Strong attention to detail, communication, and problem-solving skills help build trust and ensure effective collaboration with stakeholders. These abilities are crucial for minimizing risk, maintaining compliance, and supporting the commercial success of medical device products.

What is the difference between Contract Manager Medical Device vs Regulatory Affairs Specialist?

AspectContract Manager Medical DeviceRegulatory Affairs Specialist
CredentialsTypically requires a bachelor's degree in business, law, or related field; certifications like Certified Commercial Contracts Manager (CCCM) are commonRequires a degree in life sciences, pharmacy, or engineering; certifications like RAC (Regulatory Affairs Certification) are common
Work EnvironmentWorks primarily in legal, sales, or procurement departments within medical device companiesWorks in regulatory compliance departments, often collaborating with R&D and quality assurance teams
Employer & Industry UsageUsed across medical device manufacturers, suppliers, and healthcare organizationsUsed mainly in medical device, pharmaceutical, and biotech industries

The Contract Manager Medical Device focuses on negotiating and managing contracts related to medical devices, ensuring legal and commercial compliance. In contrast, the Regulatory Affairs Specialist ensures products meet regulatory standards for approval and market entry. Both roles are essential in the medical device industry but serve different functions related to compliance and legal agreements.

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

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

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

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

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

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

Contract Manager Medical Device jobs near you
Infographic showing various Contract Manager Medical Device job openings in Minnesota as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution.

Quality Manager - Medical Device

PMT Corporation

Chanhassen, MN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 14 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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