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Remote Medical Device Design Jobs in Wisconsin (NOW HIRING)

Security Engineer (AppSec)

Milwaukee, WI · On-site +1

$57.75 - $77.25/hr

Participate in security architecture design and application design reviews. * Provide training and ... As needed provide training on secured development principals in both remote and in person settings.

Comprehensive medical including Fertility, Adoption benefits, Dental, and Vision Insurance * Remote ... Assigns and documents device IP addresses, subnetting, and Virtual LAN (VLAN) assignments per ...

Comprehensive medical including Fertility, Adoption benefits, Dental, and Vision Insurance * Remote ... Assigns and documents device IP addresses, subnetting, and Virtual LAN (VLAN) assignments per ...

Dosimetrist - Remote

Green Bay, WI · Remote

$50.54 - $75.81/hr

... and design radiation therapy treatments for cancer patients. Position Specifics: Department ... Bachelor's Degree in Medical Dosimetry or Physics or two years experience as a Dosimetrist is ...

Salary: 130K - 200K CAD 91K - 141K USD AI & Innovation Mindset We are committed to leveraging ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

Salary: 130K - 200K CAD 91K - 141K USD AI & Innovation Mindset We are committed to leveraging ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

Salary: 130K - 200K CAD 91K - 141K USD AI & Innovation Mindset We are committed to leveraging ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

Salary: 130K - 200K CAD 91K - 141K USD AI & Innovation Mindset We are committed to leveraging ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

Salary: 130K - 200K CAD 91K - 141K USD AI & Innovation Mindset We are committed to leveraging ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

Salary: 130K - 200K CAD 91K - 141K USD AI & Innovation Mindset We are committed to leveraging ... Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment

Showing results 41-60

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?

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 Wisconsin?

The most popular types of Medical Device Design jobs in Wisconsin are:

What cities in Wisconsin are hiring for Remote Medical Device Design jobs?

Cities in Wisconsin with the most Remote Medical Device Design job openings:

Medical Writer / Clinical Document Author

micro1 AI

Green Bay, WI • Remote

$50 - $80/hr

Part-time

Posted 12 days ago


Job description

Role Title: 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 developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.