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Intent Clinical Jobs in Minnesota (NOW HIRING)

Homemaker - Casual Hours

Big Lake, MN ยท On-site

$21.50/hr

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Homemaker - Casual Hours

Delano, MN ยท On-site

$21.50/hr

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Homemaker - Casual Hours

Anoka, MN ยท On-site

$21.50/hr

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Homemaker - Casual Hours

Hinckley, MN ยท On-site

$21.50/hr

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Homemaker - Casual Hours

Anoka, MN ยท On-site

$21.50/hr

First seek to understand the other person assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. Qualifications What do I need to bring to the job?

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Homemaker - Casual Hours

Big Lake, MN ยท On-site

$21.50/hr

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Homemaker - Casual Hours

Delano, MN ยท On-site

$21.50/hr

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Homemaker - Casual Hours

Hinckley, MN ยท On-site

$21.50/hr

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Homemaker - Casual Hours

Anoka, MN ยท On-site

$21.50/hr

First seek to understand the other person - assume positive intent. * If you don't know or need ... Report changes or concerns to Clinical Manager. What do I need to bring to the job? * Interpersonal ...

Showing results 21-40

Intent Clinical information

What is an Intent Clinical?

An Intent Clinical role typically involves working within healthcare organizations to analyze, interpret, and apply clinical data to improve patient outcomes and operational efficiency. Professionals in this position may collaborate with medical staff, IT teams, and administrators to ensure that clinical practices align with both regulatory standards and the organization's objectives. They often use data analytics, clinical knowledge, and project management skills to identify areas for improvement and implement evidence-based solutions. The role may also involve training staff on new clinical protocols and monitoring the effectiveness of implemented changes.

What are the key skills and qualifications needed to thrive as an Intent Clinical professional?

To excel as an Intent Clinical professional, you need a strong background in clinical research, data analysis, and regulatory compliance, often supported by a degree in life sciences or related fields. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and relevant certifications such as GCP (Good Clinical Practice) are typically required. Attention to detail, effective communication, and problem-solving skills help distinguish top performers in this role. These capabilities are crucial for ensuring the accuracy, safety, and regulatory alignment of clinical studies.

What are some common challenges faced by Intent Clinical professionals when implementing new healthcare technologies?

Intent Clinical professionals often encounter challenges such as resistance to change from clinical staff, ensuring regulatory compliance, and integrating new technologies with existing electronic health record systems. Effective communication and collaboration between clinical teams, IT, and administration are crucial to address workflow disruptions and provide adequate training. Staying updated on industry standards and fostering a culture of continuous improvement are key strategies for overcoming these obstacles and ensuring successful technology adoption.

What is the difference between Intent Clinical vs Intent Medical Assistant?

AspectIntent ClinicalIntent Medical Assistant
CertificationsTypically requires clinical certifications or trainingRequires CMA or RMA certification
Work EnvironmentHospitals, clinics, outpatient facilitiesDoctor's offices, clinics, outpatient settings
Job ResponsibilitiesPatient assessments, clinical proceduresVital signs, administrative tasks, assisting with exams
Industry UsageHealthcare, clinical settingsHealthcare, outpatient care

Intent Clinical and Intent Medical Assistant roles share overlapping clinical skills and work in healthcare environments. However, Intent Clinical positions often involve more advanced clinical procedures and assessments, while Intent Medical Assistants focus on both clinical and administrative tasks. Understanding these differences helps job seekers identify the right role based on their certifications and career goals.

What cities in Minnesota are hiring for Intent Clinical jobs?

Cities in Minnesota with the most Intent Clinical job openings:

Infographic showing various Intent Clinical job openings in Minnesota as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Product Development Engineer III

Minnetronix Medical

Saint Paul, MN โ€ข On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 8 days ago


Key responsibilities

  • Lead the design, development, and optimization of Medical Device & Surgical Navigation products from concept through commercialization.

  • Coordinate prototyping, testing, and analysis activities to assess product performance and reliability.

  • Collaborate with cross-functional teams to support design transfer, manufacturing readiness, and product launch activities.


Job description

Exceptional People. Hard Problems. Meaningful Careers. Big Impact.
Nowhere else can you touch as many life-changing medical technologies. At Forj Medical, we work side by side with more than 100 medical device companies from startups to global giants to bring life-enhancing technologies to market. Working with us means solving hard problems with extraordinary people in a collaborative work environment. Join us.
Job Summary:
Product Development Engineer III applies advanced engineering principles and medical device product development expertise to develop and support Surgical Navigation products from concept through commercialization. This role is responsible for planning and executing engineering activities within our product development process, including design documentation, verification and validation, prototype and production-intent builds, and cross-functional project execution.
This role works independently on complex technical assignments and collaborates with both our external customers and internal Quality, Regulatory, Operations, Commercial Team and Supply Chain teams to ensure product requirements are met while maintaining compliance with design control and quality system requirements. It requires strong technical judgment, problem-solving skills, and the ability to drive project deliverables with limited supervision.
Job Duties and Responsibilities:
Product Development
  • Lead the design, development, and optimization of Medical Device & Surgical Navigation products, components, assemblies, and subsystems from concept through commercialization.
  • Translate customer, user, and clinical needs into product requirements, engineering specifications, and design inputs.
  • Perform concept development, feasibility assessments, risk analyses, and design reviews.
  • Coordinate prototyping, testing, and analysis activities to assess product performance and reliability.
  • Evaluate design alternatives and implement solutions that optimize performance, reliability, manufacturability, and usability.
  • Troubleshoot complex technical challenges and drive effective resolutions.
  • Support Voice of Customer (VOC) activities and apply market and clinical insights to product development.
  • Ensure compliance with applicable medical device regulations, design controls, risk management processes, and quality system requirements.

Engineering Documentation
  • Create and maintain engineering documentation including CAD models, drawings, GD&T specifications, BOMs, product specifications, test protocols, test reports, and DHF deliverables.
  • Ensure documentation is complete, accurate, and compliant with quality system requirements.
  • Support design verification and validation activities through timely and thorough documentation.

Design Verification & Validation
  • Develop and execute verification and validation strategies, plans, protocols, and reports.
  • Define test methods, acceptance criteria, and data collection approaches to demonstrate compliance with product requirements.
  • Analyze test results, resolve identified issues, and present findings during technical and design reviews.

Verification & Validation Builds
  • Coordinate prototype, engineering, and production-intent builds.
  • Partner with Operations, Manufacturing Engineering, Supply Chain, and Quality to ensure build readiness and successful execution.
  • Track build outcomes, document findings, and drive issue resolution.

Cross-Functional Collaboration
  • Collaborate with Quality, Regulatory, Clinical, Marketing, Manufacturing, Supply Chain, Program Management, and Operations teams to achieve project objectives.
  • Support design transfer, manufacturing readiness, and product launch activities.
  • Communicate project status, technical risks, and mitigation plans to stakeholders.

Contribute to continuous improvement initiatives that enhance product quality and development efficiency
Qualifications
Required
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related engineering discipline.
  • 5+ years of product development experience, preferably in the medical device industry.
  • Experience developing mechanical and/or electromechanical products in a regulated environment.
  • Strong knowledge of design controls, risk management, and regulated product development processes.
  • Expertise in product design, DFx, materials selection, manufacturing processes, and mechanical problem-solving.
  • Experience creating engineering documentation, including drawings, specifications, BOMs, DHF deliverables, and verification/validation documentation.
  • Proficiency with SolidWorks or similar 3D CAD software, including GD&T and engineering drawing creation.
  • Experience with prototyping, verification and validation testing, root-cause analysis, and technical troubleshooting.
  • Strong technical writing, analytical, and problem-solving skills.
  • Proficiency with Microsoft Office Suite.
  • Ability to independently manage technical work and collaborate effectively within cross-functional teams.
  • Experience supporting FDA submissions, including 510(k) and/or PMA programs.

Preferred
  • Experience developing Surgical Navigation, image-guided surgery, or capital medical equipment products.
  • Medical device manufacturing experience.
  • Knowledge of FDA QSR, ISO 13485, IEC 60601, and other applicable medical device standards.
  • Experience supporting design transfer and manufacturing readiness.
  • Experience with machine shop operations, injection molding, and additive manufacturing.
  • Familiarity with requirements management, FMEA, statistical analysis, Microsoft Project, and Minitab.

Salary: $85,000-$115,000
EEO Statement
Forj Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Employment Requirement
Must be authorized to work in the United States.
Compensation and Total Rewards Package
The salary range for this position is outlined below under "Job Details" and is dependent upon the individual's skills, experience, qualifications, and applicable employment laws. Beyond base salary, Forj offers a competitive Total Rewards Package. We offer health, dental, vision, 401K plans, and time off programs. You may also be eligible to participate in an annual bonus program which depends on various factors, including, individual and organizational performance.