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Contract Method Validation Jobs in Minnesota (NOW HIRING)

Test Technician

Minneapolis, MN · On-site

$30 - $35/hr

Medical Device Manufacturing Company Duration: 12-Month Contract Location: Minneapolis, MN 55432 ... Support test method validation, equipment qualification, and software validation activities ...

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Test Technician

Minneapolis, MN · On-site

$25 - $30/hr

... a contract Test Technician . This is an exciting opportunity for a self-motivated technician to ... method validation, equipment qualification and equipment software validation studies in ...

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CCI Technology Lead

Eden Prairie, MN · On-site

$120K - $140K/yr

Lead and support method validation activities and method transfer projects * Interpret test results ... Experience in CDMO or contract testing laboratory environment required * Knowledge and ...

Medical Lab Scientist Lead

Minneapolis, MN · On-site

$40.17 - $53.97/hr

Day (United States of America) Shift Length: 8 hour shift Hours Per Week: 40 Union Contract: SEIU-9 ... May be the document owner of technical procedures, forms, misc. documents, method validation, and ...

$40.17 - $53.97/hr

Day (United States of America) Shift Length: 8 hour shift Hours Per Week: 40 Union Contract: SEIU-9 ... May be the document owner of technical procedures, forms, misc. documents, method validation, and ...

Manufacturing Engineer

Minneapolis, MN

$76K - $98K/yr

Prepare validation protocols and reports to clearly communicate test methods, results, and ... Experience working in a catheter-focused contract manufacturing environment is highly beneficial.

... for contract manufacturing of medical device components. This role serves as a key technical ... Support Gage R&R completion and Test Method Validations * Support Corrective and Preventive Actions

... for contract manufacturing of medical device components. This role serves as a key technical ... Support Gage R&R completion and Test Method Validations * Support Corrective and Preventive Actions

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Contract Method Validation information

What is the difference between Contract Method Validation vs Analytical Method Validation?

AspectContract Method ValidationAnalytical Method Validation
PurposeValidates that a contracted method meets specific requirements for a particular project or clientEnsures an analytical method is accurate, reliable, and reproducible for testing purposes
ScopeTypically project-specific, focusing on methods used under contractual agreementsBroader, covering method development, validation, and routine testing
CredentialsOften requires validation expertise, GMP knowledge, and industry-specific certificationsRequires analytical chemistry knowledge, validation experience, and relevant certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing settings with client-specific projectsLaboratories performing routine testing and method development in similar industries

Contract Method Validation focuses on validating methods for specific client projects, while Analytical Method Validation ensures the overall reliability of testing methods used routinely in laboratories. Both roles require similar credentials and work in related environments, but their scope and purpose differ.

What cities in Minnesota are hiring for Contract Method Validation jobs?

Cities in Minnesota with the most Contract Method Validation job openings:

Infographic showing various Contract Method Validation job openings in Minnesota as of August 2026, with employment types broken down into 89% Full Time, 3% Part Time, and 8% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.

Mechanical Engineer - Medical Device (Onsite - Arden Hills, MN) Contract with Possible Extension

Pharmavise

Saint Paul, MN • On-site

Full-time

Re-posted 27 days ago


Job description


Our F500 Medical Device client has an exciting opportunity for a Mechanical Engineer.
Job Summary:
The Urology Research & Development (R&D) organization is seeking a highly skilled and motivated Mechanical Engineer to join our acquisition and integration project for a duration of twelve months, with the option to extend. In this role, you will provide support in validating existing test methods to the client's compliance using Gauge R&R or other methods. This role would be responsible for assessing the acquired company's design test methods to determine if validation testing is required and either running the appropriate tests or updating associated documentation to rationalize why no testing is required.
As a key team member, you will provide testing solutions and technical support under some guidance from our subject matter experts.You will utilize your background in mechanical and/or systems design, test method design and validation, verification testing, and statistical analysis.
Responsibilities:
  • Identifying gaps in the acquired company's test method validation compliance to the client's Work Instructions and SOPs and defining strategy to close these gaps.

  • Providing input to project goals and progress and recommending appropriate revisions.

  • Communicating progress, risks, and trade-offs of technical deliverables to project leadership, and recommends revisions as needed.

  • Completing complex or novel assignments requires the development of new or improved techniques and procedures. Work is expected to result in efficient and effective integration of medical device technologies into the client's portfolio.

  • Completing engineering work in one or more of the following: technology development or remediation, product design refinement, test of materials, preparation of specifications, process study, and report preparation.

  • Assessing the feasibility and soundness of alternative engineering processes, products, or equipment.

  • Successfully completed clear and concise engineering documentation.

  • Demonstrating Technology Development and Product Development system knowledge through delivery of high quality, high impact deliverables.

Job Requirements:
  • Windchill and Test Method Validation experience required

  • BS or above in Mechanical Engineering, Biomedical Engineering, Electromechanical Engineering, or related field

  • 4+ yrs of engineering or related experience with bachelor's degree, or 2+ yrs with Master's

  • Strong mechanical and/or systems engineering and problem-solving skills and attention to detail

  • Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources

  • Strong written and verbal communication, judgment, decision-making, collaboration, and critical thinking skills

  • Personal drive, individual accountability & a strong bias for action.

  • 10% travel

  • Must work onsite 3 days per week minimum at our Arden Hills, MN location

Preferred Qualifications:
  • Familiarity with IEC 14708 and 45502 Active Implantable standards

  • Familiarity with IEC 60601 Medical Electrical Equipment standards, including laser-specific sections

  • Experience with statistical techniques (Gauge R&R, Process Capabilities Studies) and Minitab

  • Experience in single-use device or active implantable test methods and test method validation

  • Ability to build strong relationships across the organization and with external stakeholders

Other Details:
  • Schedule: 06:00:AM - 02:30:PM

  • Contract Length: 12 months with possible extension

  • Work Set-Up: Onsite 3 days per week minimum in Arden Hills, MN

  • Start Date: 12/1/2025

  • Travel Requirements: 10%