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Remote Medical Device Technical Writer Jobs in Minnesota

Provide technical guidance and mentorship to Packaging Engineers and Associate Packaging Engineers ... Preferred Qualifications * 5+ years of medical device packaging experience or related medical ...

New

Provide technical guidance and mentorship to Packaging Engineers and Associate Packaging Engineers ... Preferred Qualifications * 5+ years of medical device packaging experience or related medical ...

New

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

Medical writing experience with US and EU regulatory requirements understanding in medical device ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

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 ...

About the company: Viant is a global medical device partner providing design, development ... Work Model: Remote * Preferred locations: US Midwest/Northeast cities Key Responsibilities:

SR Automation Engineer

Hutchinson, MN · On-site +1

$106K - $139K/yr

Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ... Selects process improvement techniques to solve technical problems and makes sound equipment and ...

SR Automation Engineer

Blaine, MN · On-site +1

$102K - $134K/yr

Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ... Selects process improvement techniques to solve technical problems and makes sound equipment and ...

SR Automation Engineer

Blaine, MN · On-site +1

$88K - $124K/yr

Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're ... Selects process improvement techniques to solve technical problems and makes sound equipment and ...

Showing results 41-60

Remote Medical Device Technical Writer information

What is the difference between Remote Medical Device Technical Writer vs Remote Regulatory Affairs Specialist?

AspectRemote Medical Device Technical WriterRemote Regulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences, engineering, or related field; certifications like RMT or technical writing certifications are commonRequires degrees in life sciences, law, or regulatory fields; certifications like RAC are often preferred
Work EnvironmentPrimarily writes and edits technical documents remotely for medical device companiesFocuses on regulatory submissions, compliance, and communication with authorities, often remotely
Industry UsageUsed across medical device companies, biotech, and healthcare tech firmsCommon in medical device, pharmaceutical, and biotech industries

While both roles require knowledge of medical devices and regulatory standards, the Remote Medical Device Technical Writer primarily creates technical documentation, whereas the Remote Regulatory Affairs Specialist manages regulatory compliance and submissions. Both roles often work remotely and require relevant industry experience, but their core responsibilities differ significantly.

What are the most commonly searched types of Medical Device Technical Writer jobs in Minnesota?

The most popular types of Medical Device Technical Writer jobs in Minnesota are:

What are popular job titles related to Remote Medical Device Technical Writer jobs in Minnesota?

For Remote Medical Device Technical Writer jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Remote Medical Device Technical Writer jobs in Minnesota look for?

The top searched job categories for Remote Medical Device Technical Writer jobs in Minnesota are:

What cities in Minnesota are hiring for Remote Medical Device Technical Writer jobs?

Cities in Minnesota with the most Remote Medical Device Technical Writer job openings:

Principal Packaging Engineer

Medtronic

Fridley, MN • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Key responsibilities

  • Lead the design, development, and verification of packaging systems and components for sterile medical devices.

  • Develop and execute packaging verification strategies, including protocol development, testing, analysis, and technical reporting.

  • Partner with cross-functional teams to support product commercialization, sustaining engineering, and continuous improvement initiatives.


Medtronic rating

7.9

Company rating: 7.9 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

154th of 545 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 16 Sep 2026


Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the LifeThe Principal Packaging Engineer is a key member of the Packaging Development function, supporting the design, development, verification, and continuous improvement of packaging systems for sterile medical devices. This role partners with cross-functional teams to commercialize new products, enhance existing packaging solutions, and ensure compliance with regulatory and quality requirements across the product lifecycle.
This position may be based in Rice Creek (West), MN or Plymouth (Berkshire), MN and follows a flex work model with four days onsite and one day remote each week. Up to 10% travel may be required in this role.

The Principal Packaging Engineer leads packaging development activities for sterile medical devices, supporting both new product development and sustaining engineering initiatives. This roleis responsible fordesigning and verifying packaging systems, driving process and material improvements, and providing technical leadership on packaging-related projects. The individual will work independently, collaborate across functions, and help advance packaging technologies that meet customer, patient, quality, and regulatory requirements.

Primary Responsibilities

  • Lead the design, development, and verification of packaging systems and components for sterile medical devices, includingproducts sterilizedusing Ethylene Oxide, Steam, and Gamma methods.

  • Develop and execute packaging verification strategies, including protocol development, testing, analysis, and technical reporting to support product release.

  • Evaluate packaging materials and processes and implement improvements that enhance product quality, performance, manufacturability, and compliance.

  • Partner with cross-functional teams to support product commercialization, sustaining engineering, and continuous improvement initiatives.

  • Manage shelf-life and biocompatibility testing activities for new packaging material combinations and packaging system changes.

  • Apply Food and Drug Administration (FDA), International Organization for Standardization (ISO), and packaging industry requirements to ensure compliant package design and validation.

  • Support supplier selection, qualification, and material approval activities while serving as a technical liaison with packaging vendors.

  • Provide technical guidance and mentorship to Packaging Engineers and Associate Packaging Engineers as needed.

Required Qualifications

  • Bachelor's degree with 7+ years of professional experience, or advanced degree with 5+ years of professional experience.

  • Experience developing,validating, or supporting packaging systems for regulated products.

  • Experience authoring technical documentation, including protocols, reports, specifications, orvalidationdocumentation.

  • Experience supporting Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities.

Preferred Qualifications

  • 5+ years of medical device packaging experience or related medical device industry experience.

  • Experience working with ISO, ASTM International (ASTM), and packaging-related standards.

  • Working knowledge of project management methodologies and tools.

  • Experienceidentifying, evaluating, and implementing process or material improvements.

  • Demonstrated analytical, decision-making, written communication, and verbal communication skills.

  • Ability to work independently and collaborate effectively with cross-functional stakeholders.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind:


Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.


Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.


If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.


If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD):$124,000.00 - $186,000.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.


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