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Medical Manufacturing Jobs in Rochester, MN (NOW HIRING)

Manufacturing Engineer

Rochester, MN

$71.30K - $91.80K/yr

Experience in a medical device manufacturing environment. * Experience with Design for Manufacturability (DFM) and collaboration with Test Engineering on Design for Testability (DFT), particularly ...

Manufacturing Engineer

Rochester, MN

$71.30K - $91.80K/yr

Experience in a medical device manufacturing environment. * Experience with Design for Manufacturability (DFM) and collaboration with Test Engineering on Design for Testability (DFT), particularly ...

Manufacturing Engineer II

Rochester, MN · On-site

$74.20K - $95.60K/yr

... medical, and semiconductor capital equipment. We prioritize career growth, fostering a culture that ... Summary: Provides technical manufacturing liaison required for the production of high quality ...

Supervisor I, Manufacturing

Rochester, MN · On-site

$63.33K - $79.99K/yr

... medical, and semiconductor capital equipment. We prioritize career growth, fostering a culture that ... manufacturing and quality standards to ensure acceptability • Reviews and compiles operations ...

Manufacturing Technician II

Rochester, MN · On-site

$24.26 - $30.33/hr

... medical, and semiconductor capital equipment. We prioritize career growth, fostering a culture that ... The manufacturing Technician provides and supports manufacturing equipment, materials and processes ...

Scientist This role focuses on manufacturing and testing performance of therapeutic products in ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

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How much do medical manufacturing jobs pay per hour?

As of May 31, 2026, the average hourly pay for medical manufacturing in Rochester, MN is $18.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.96 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Manufacturing, and why are they important?

To thrive in Medical Manufacturing, you need a background in manufacturing processes, quality control, and knowledge of medical device regulations, often supported by a relevant degree or technical training. Familiarity with standards such as ISO 13485, Good Manufacturing Practices (GMP), and operation of specialized production equipment is typically required. Attention to detail, problem-solving, and strong teamwork skills help ensure compliance and efficient production. These competencies are crucial to consistently produce safe, effective products and maintain regulatory compliance in a highly regulated industry.

What are some common challenges faced in medical manufacturing roles, and how can new employees prepare for them?

One of the main challenges in medical manufacturing is maintaining strict compliance with regulatory standards, such as FDA or ISO requirements, which necessitates meticulous attention to detail and thorough documentation. Employees must also adapt to rapidly evolving technologies and processes to ensure high-quality, safe products. Newcomers can prepare by familiarizing themselves with industry regulations, developing strong organizational skills, and being open to ongoing training. Collaboration with quality assurance, engineering, and production teams is also key to overcoming these challenges and ensuring smooth operations.

What is medical manufacturing?

Medical manufacturing refers to the process of designing, producing, and distributing medical devices, equipment, and supplies used in healthcare settings. This industry covers a wide range of products, from simple items like syringes to complex devices such as MRI machines and surgical robots. Medical manufacturers must adhere to strict quality standards and government regulations to ensure the safety and effectiveness of their products. The field plays a crucial role in supporting patient care and advancing medical technology.

What is the difference between Medical Manufacturing vs Medical Assembly?

AspectMedical ManufacturingMedical Assembly
CertificationsOften requires GMP, ISO, and industry-specific certificationsMay require similar certifications but focuses more on assembly procedures
Work EnvironmentFactories, cleanrooms, production linesAssembly lines, cleanrooms, quality control areas
Employer & Industry UsageMedical device companies, pharmaceutical firmsMedical device manufacturers, hospitals, clinics
Job FocusDesign, production, and quality control of medical devicesAssembling and testing medical devices or components

Medical Manufacturing involves the broader process of designing, producing, and ensuring quality of medical devices, often requiring specialized certifications. Medical Assembly is more focused on the hands-on process of putting together and testing these devices. Both roles are essential in the medical industry and share similar work environments and certifications, but they differ in scope and daily tasks.

What cities near Rochester, MN are hiring for Medical Manufacturing jobs? Cities near Rochester, MN with the most Medical Manufacturing job openings:
Infographic showing various Medical Manufacturing job openings in Rochester, MN as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $39,179 per year, or $18.8 per hour.
Manufacturing Engineer

Manufacturing Engineer

Actalent

Rochester, MN

$71.30K - $91.80K/yr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday


Job description

Manufacturing Engineer

Job Description:

The Manufacturing Engineer takes full ownership of manufacturing activities, guiding products from prototype through pilot and full production builds. This role focuses on improving manufacturing processes, supporting new product launches, and driving continuous quality improvement using structured methodologies and statistical tools. The position requires close collaboration with cross-functional teams and customers to ensure robust, efficient, and cost-effective manufacturing solutions.

Responsibilities:

  • Take full manufacturing responsibility for assigned products, leading them through prototype, pilot, and production builds.
  • Oversee the implementation of customer documentation changes and internal change orders to ensure accurate and timely updates to production processes.
  • Report on the status of new product launch (NPL) activities and communicate progress to relevant stakeholders.
  • Use statistical tools to lead quality improvement initiatives within the customer team and production environment.
  • Drive internal and external corrective action plans to address quality and process issues.
  • Actively participate in new customer development and new business development activities by providing manufacturing expertise and input.
  • Analyze line return information to identify manufacturing process issues and drive appropriate corrective actions.
  • Perform product-level engineering support as required to resolve production problems and optimize performance.
  • Perform all essential functions and competencies listed for the role.
  • Conduct Design for Manufacturability (DFM) reviews and collaborate with Test Engineering on Design for Testability (DFT).
  • Assist in developing project proposals and associated cost estimates, providing accurate manufacturing input.
  • Execute product transitional manufacturing requirements and define process approaches to support smooth transfers into production.
  • Develop in-depth knowledge of customer products as required to support transitional activities and ongoing production support.
  • Document and resolve moderately complex cross-departmental and cross-functional issues using structured problem-solving tools.
  • Collaborate effectively with internal and external customers, providing clear communication, presentations, and technical support.
  • Contribute to continuous improvement initiatives, including lean manufacturing and process optimization projects.

Essential Skills:

  • Bachelor of Science degree in Engineering.
  • Minimum of 5+ years of experience as a manufacturing engineer in a production setting.
  • Hands-on experience in manufacturing engineering, process engineering, and manufacturing process development and support.
  • Demonstrated ability to solve and document moderately complex cross-departmental issues using structured problem-solving tools.
  • Engineering-level understanding of electronic components, circuits, and systems or mechanical components and systems, depending on education and experience.
  • Experience with continuous improvement, lean manufacturing, and Six Sigma or Lean Six Sigma methodologies.
  • Proven capability in process improvement and project management within a manufacturing environment.
  • Experience with assembly processes and creation or maintenance of work instructions.
  • Excellent written and verbal communication skills.
  • Effective interpersonal skills with the ability to work with diverse groups and interact with internal and external customers.
  • Strong multitasking skills with the ability to take on additional responsibilities as required.
  • Effective organization and prioritization skills with demonstrated high attention to detail.
  • Ability to work with minimal supervision and guidance, exercising discretion, independent judgment, and professionalism.
  • Understanding of and ability to use continuous improvement tools to enhance quality, efficiency, and throughput.
  • Strong customer service orientation and client focus.
  • Working knowledge of productivity tools, including Microsoft Office products and WebEx conferencing software.

Additional Skills & Qualifications:

  • Experience in a medical device manufacturing environment.
  • Experience with Design for Manufacturability (DFM) and collaboration with Test Engineering on Design for Testability (DFT), particularly for Level II responsibilities.
  • Ability to assist in developing project proposals and cost estimates related to manufacturing activities.
  • Experience executing transitional manufacturing requirements and defining process approaches for new or transferred products.
  • Demonstrated ability to document and resolve moderate to complex cross-functional challenges using structured problem-solving tools.
  • Demonstrated discretion, confidentiality, and professionalism when handling sensitive information and customer interactions.
  • Proven ability to build in-depth knowledge of customer products to support transitional and ongoing manufacturing activities. #mneng26
Job Type & Location

This is a Contract position based out of Rochester, MN.

Pay and Benefits

The pay range for this position is $38.00 - $55.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Rochester,MN.

Application Deadline

This position is anticipated to close on Jun 9, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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