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Process Development Manufacturing Engineer Jobs in Minnesota

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Our business is expanding and we are seeking a Manufacturing / Process Development Engineer to support our increasing demand and implementation of new medical device products to market. The qualified ...

Manufacturing Engineer

Plymouth, MN · On-site

$77K - $99K/yr

Process Development, Characterization & Validation ( IQ/OQ/PQ ) * Test Fixture Design * Test Method & Inspection Method Development/Validation * Manufacturing Processes & Product Development ...

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Manufacturing Engineer

Minneapolis, MN · On-site

$76K - $98K/yr

Manufacturing Engineer Minneapolis, MN | Direct Hire | $85,000-$95,000 | 100% Onsite Konik is ... Experience supporting new product introductions, process development, tooling, fixtures, and ...

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Process Development Manufacturing Engineer information

What cities in Minnesota are hiring for Process Development Manufacturing Engineer jobs?

Cities in Minnesota with the most Process Development Manufacturing Engineer job openings:

Infographic showing various Process Development Manufacturing Engineer job openings in Minnesota as of June 2026, with employment types broken down into 1% As Needed, 84% Full Time, and 15% Part Time. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Manufacturing & Process Development Engineer

White Bear Lake, MN • On-site

$80K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 hours ago

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Key responsibilities

  • Support the development and validation of new manufacturing processes and design changes for medical devices.

  • Monitor equipment and process performance, troubleshoot issues, and perform root cause analysis.

  • Collaborate with cross-functional teams to ensure manufacturability, develop automation and fixtures, and support process validation activities.


Job description

Fiagon NA, LLC designs, develops, manufactures, and markets advanced medical devices for use in the healthcare industry. Our business is expanding and we are seeking a Manufacturing / Process Development Engineer to support our increasing demand and implementation of new medical device products to market.


The qualified candidate will provide a role leading engineering initiatives in developing new product & manufacturing processes as well as support & implement improvements across several existing product manufacturing areas. This role will interface in a collaborative team-based environment with research & development, operations, quality, regulatory, sales, and marketing teams to support our existing business and drive the successful implementation & launch of new medical devices.


This role requires onsite work. There is a great amount of growth opportunity within the organization and the right candidate will have exposure to a large variety of internally manufactured products and opportunity to help shape the organization.


The responsibilities of this position include:

·        Monitor performance of equipment and processes, providing troubleshooting and root cause analysis of non-conformances, low yields, or other quality/production issues

·         Define, verify, and validate new manufacturing processes and design changes to existing products

·         Develop and execute product/process testing protocols and document results

·         Collaborate with quality and development engineering to create and ensure manufacturability of new medical device related products

·         Develop and collaborate on the creation of automation, manufacturing fixtures, & equipment

·         Develop and execute equipment qualifications (IQ/OQ)

·         Contribute to development and execution of process validation activities

·         Identify and implement areas of continuous improvement for current product production

·         Train and/or provide work direction to manufacturing operators and technicians

·         Provide product specific technical support as needed

·        Work with vendors/suppliers on technical design, procurement, and fabrication of materials, equipment, fixturing, etc.

·         Lead and/or support projects or project teams, as needed

·         Understand and comply with ISO 13485, FDA, and CE requirements

·         Generate and maintain all aspects of design history records per the Fiagon Quality Management System for all engineering-based activities related to new and existing products

Position Requirements:

·         Bachelor’s degree in Mechanical Engineering or related discipline

·         Prior experience with medical device product manufacturing and development. Balloon catheter development and balloon molding development is a plus.  

·         Ability to work in a fast-paced, dynamic work environment with a focus on technical excellence, responsiveness to customer needs and innovative thinking is required 

·         Mechanical aptitude with the ability to understand and optimize manufacturing processes

·         Strong technical writing skills: Ability to write protocols, reports, manufacturing procedures, and supporting documentation.

·         Hands on experience with fabrication of assembly fixtures, equipment, and test samples

·         CAD experience, creation of parts and engineering spec prints

·         Demonstrated knowledge of developing products within the framework of a QMS

·         Critical thinking skills with the ability to solve problems and explain solutions

·         Ability to manage multiple tasks simultaneously, establishing project plans, achieve timelines, and communicating results

·         Strong organizational skills and attention to detail

·         Excellent written and oral communication skills


Fiagon NA, LLC, believes in the synergy of teamwork while maintaining an entrepreneurial spirit and providing an environment in which our associates develop and accomplish professional objectives. We offer a competitive salary and benefits package including health, life, retirement and related benefits.