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Remote Medical Device Design Jobs in Minnesota (NOW HIRING)

Project Manager, Engineering

Alpharetta, GA · On-site +1

$116K - $174K/yr

This position will be remote. The candidate need to be within commuting distance of our office in ... of medical device quality systems and regulatory requirements (e.g., design controls, DHF/DMR ...

Director - Product Security

Minneapolis, MN · On-site +1

$243K - $254K/yr

... posture of our medical device portfolio throughout its entire lifecycle, from design and ... Houston, TX is the ideal location for this role, but this is open to Remote opportunities for well ...

Medical Device Manufacturing Company Duration: 3 Months (possible extension) Location: 100% Remote Shift: 1st Shift | 8:00 AM - 5:00 PM CST Role Overview: Responsible for end-to-end payroll analysis ...

SQL Developer

Moundsview, MN · Remote

$48 - $65.75/hr

Work as a Database Administrator for a leading Medical Device company to alleviate pain, restore ... You will support a Web Based Remote Patient Management System used by our clinicians on behalf of ...

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Remote Medical Device Design information

What is remote medical device design?

Remote medical device design refers to the process of developing and engineering medical devices while working from a location outside of a traditional office or laboratory, often using digital collaboration tools. Professionals in this field may design, prototype, test, and iterate devices such as diagnostic tools, monitoring equipment, or implants, all while collaborating with teams virtually. This approach allows for greater flexibility, access to global talent, and the ability to quickly adapt to changes in project requirements or regulatory standards. Remote medical device designers need strong communication skills, technical expertise, and familiarity with relevant regulations and standards.

What is the difference between Remote Medical Device Design vs Remote Medical Device Manufacturing?

AspectRemote Medical Device DesignRemote Medical Device Manufacturing
Primary FocusConcept development, product design, prototypingProduction, assembly, quality control
Required SkillsCAD, biomedical engineering, regulatory knowledgeManufacturing processes, quality assurance, equipment operation
Work EnvironmentDesign studios, labs, remote collaborationFactories, production lines, remote monitoring
CertificationsBiomedical engineering, FDA regulationsISO standards, manufacturing certifications

Remote Medical Device Design focuses on creating and developing new medical devices, while Remote Medical Device Manufacturing involves producing and assembling these devices. Both roles require specialized knowledge and often collaborate closely, but they differ in their core activities and skill sets.

What are some common challenges encountered when designing medical devices remotely, and how can they be addressed?

One of the main challenges in remote medical device design is effective collaboration, especially when teams are distributed across different time zones and may have limited access to physical prototypes. To address this, teams often rely on advanced digital collaboration tools, virtual whiteboards, and cloud-based CAD platforms to share designs and feedback in real time. Regular virtual meetings and clear documentation protocols are essential for maintaining alignment and ensuring regulatory compliance. Additionally, early and frequent communication with manufacturing and regulatory specialists helps to anticipate and resolve potential issues before they become major obstacles.

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

To thrive as a Remote Medical Device Designer, you need expertise in biomedical engineering, product development, and regulatory standards, often supported by a relevant engineering degree. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulations is typically required. Excellent problem-solving, communication, and project management skills help in collaborating virtually with cross-functional teams. These skills ensure innovative, compliant device designs that meet clinical needs and succeed in competitive markets.
What are the most commonly searched types of Medical Device Design jobs in Minnesota? The most popular types of Medical Device Design jobs in Minnesota are:
What cities in Minnesota are hiring for Remote Medical Device Design jobs? Cities in Minnesota with the most Remote Medical Device Design job openings:
Infographic showing various Remote Medical Device Design job openings in Minnesota as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.
Project Manager, Engineering

Project Manager, Engineering

Medline

Alpharetta, GA • On-site, Remote

$116K - $174K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 26 days ago


Medline Industries rating

7.5

Company rating: 7.5 out of 10

Based on 249 frontline employees who took The Breakroom Quiz

256th of 528 rated manufacturers


Job description

Job Summary

JOB SUMMARY:
The PMO Engineer partners closely with engineering, quality, operations, and senior leadership to manage complex, cross-functional, medical device new product introductions (NPI). The role is responsible for advancing PMO maturity through the development and deployment of standardized tools, templates, and reporting frameworks, while ensuring alignment with regulatory requirements such as design controls, change management, and document control (e.g., DHF/DMR).
Responsible for managing and communicating project definition, development milestones, project schedules, and project statuses in the development of Engineering and Operational plant projects. Coordinate and manage large scale manufacturing and for Medline Industries both domestic and international.
This position will be remote. The candidate need to be within commuting distance of our office in Eagan, MN or Alpharetta, GA.

Job Description

CORE JOB RESPONSIBILITIES:

Determines project responsibilities by identifying project phases and is responsible for identifying key stakeholders and obtaining their collaboration. Creates and maintains comprehensive project documentation inside design controls.
Establishes schedules and project plans and specifications for all assigned projects. Measure and report on status of the project both financially and go-live dates
Set Project specifications by studying project requirements, and standards; completing technical studies and developing preparing cost estimates.
Coordinate and influence cross-functional teams and external partners (e.g., vendors), ensuring accountability, alignment, and timely execution of engineering and manufacturing projects.
Establish and enforce compliant project documentation practices, including oversight of drawings, specifications, and engineering change records, ensuring adherence to quality system requirements (e.g., DHF/DMR, change control).
Prepare status reports by summarizing information and reporting to upper management.

MINIMUM JOB REQUIREMENTS:

Education
Bachelor's degree.
Relevant Work Experience
6+ years of progressive experience in project management or PMO roles within a regulated industry, preferably medical device, life sciences, or pharmaceutical manufacturing.
Additional
Proven ability to manage multiple projects and priorities with a high degree of autonomy and accountability.
Ensure that all projects are delivered on-time, within scope and within budget.
Assist in the project scope and objectives, involving all related parties ensuring technical and tangible feasibility.
Support securing project approval
Measure project performance and report accordingly to senior management
Perform risk management to mitigate risks, for both the project and any potential risk to business operations.
This position will require approximately up to 25% domestic and limited international travel.
Advanced skill level in Microsoft Project or similar program.

PREFERRED QUALIFICATIONS:
Relevant Work Experience Certification / Licensure
Six Sigma Black Belt or higher certification a plus
Advanced degree or PMP certification preferred.
Strong working knowledge of medical device quality systems and regulatory requirements (e.g., design controls, DHF/DMR, change management, CAPA, validation processes).
Demonstrated experience leading complex, cross-functional projects focused on NPI.
Strong analytical, problem-solving, and risk management skills with the ability to translate data into actionable insights.
Excellent communication and stakeholder management skills, including experience presenting to senior leadership.
Experience mentoring or leading less experienced team members and driving process improvements within a PMO structure.

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The anticipated salary range for this position:

$116,000.00 - $174,000.00 Annual

The actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.

We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging pagehere.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.


What Medline Industries employees say

Pay

Benefits

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Workplace

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About Medline

Sourced by ZipRecruiter

Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Winnetka, IL, US

Year founded

1966