... Engineer (PPDE) and Subject Matter Expert (SME) for extrusion technologies across our manufacturing ... medical device manufacturing. The ideal candidate will bring deep technical expertise, a track ...
... Engineer (PPDE) and Subject Matter Expert (SME) for extrusion technologies across our manufacturing ... medical device manufacturing. The ideal candidate will bring deep technical expertise, a track ...
This role serves as the technical authority for DevOps, CI/CD, release engineering, and operational infrastructure within a regulated medical device environment. At Orthogrid Systems, we develop ...
This role serves as the technical authority for DevOps, CI/CD, release engineering, and operational infrastructure within a regulated medical device environment. At Orthogrid Systems, we develop ...
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Education Bachelor's or higher 5-6 years of experience Med Device required Job Summary: This ... Applied knowledge of applicable quality, engineering, regulatory, Corporate and/or Unit ...
Engr 3, Quality
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The position requires good knowledge of the disciplines within a medical device QMS and knowledge ... Implement quality engineering tools in the operation to drive methodical and process-based ...
Senior Engineer, Quality - Sustaining & Validation
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The position requires good knowledge of the disciplines within a medical device QMS and knowledge ... Implement quality engineering tools in the operation to drive methodical and process-based ...
The position requires good knowledge of the disciplines within a medical device QMS and knowledge ... Implement quality engineering tools in the operation to drive methodical and process-based ...
The position requires good knowledge of the disciplines within a medical device QMS and knowledge ... Implement quality engineering tools in the operation to drive methodical and process-based ...
... Engineer (PPDE) and Subject Matter Expert (SME) for extrusion technologies across our manufacturing ... medical device manufacturing. The ideal candidate will bring deep technical expertise, a track ...
... Engineer (PPDE) and Subject Matter Expert (SME) for extrusion technologies across our manufacturing ... medical device manufacturing. The ideal candidate will bring deep technical expertise, a track ...
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... medical device environment. This role requires strong technical expertise in Design Controls, Risk Management, Verification & Validation (V&V), and Technical Risk Management (TRM/TMV) , with the ...
Quick apply
Quality Engineer
West Valley City, UT · On-site
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... medical device environment. This role requires strong technical expertise in Design Controls, Risk Management, Verification & Validation (V&V), and Technical Risk Management (TRM/TMV) , with the ...
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Manufacturing Engineer Metals Processing
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Bachelor's degree in Mechanical, Aerospace, Materials Science, Chemical, or related Engineering ... Experience in regulated manufacturing (Medical Device preferred; Pharma, Aerospace, Automotive, or ...
Manufacturing Engineer Metals Processing
Draper, UT · On-site
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... Engineer, and more * Gain hands-on experience working closely as a part of an engineering team to develop, test, and implement designs pertaining to advanced medical device technology to address ...
Engineering Co-Op Program, Spring-Summer 2027
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... Engineer, and more * Gain hands-on experience working closely as a part of an engineering team to develop, test, and implement designs pertaining to advanced medical device technology to address ...
Bioengineering Intern
Logan, UT · On-site
$13 - $17.25/hr
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Bioengineering Intern
Logan, UT · On-site
$13 - $17.25/hr
Summary Applies knowledge of engineering, biology, and biomechanical principles to support the ... Currently pursuing a Bachelor's degree or equivalent in medical technology, medical device, biology ...
Bioengineering Intern
$13 - $17.25/hr
Summary Applies knowledge of engineering, biology, and biomechanical principles to support the ... Currently pursuing a Bachelor's degree or equivalent in medical technology, medical device, biology ...
Bioengineering Intern
$13 - $17.25/hr
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Bioengineering Intern
Logan, UT · On-site
$13 - $17.25/hr
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Quick apply
Bioengineering Intern
Logan, UT · On-site
$13 - $17.25/hr
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What You Can Expect The Principal Software Quality Engineer supports the design, development, and lifecycle support of medical device software, including software incorporating artificial ...
What You Can Expect The Principal Software Quality Engineer supports the design, development, and lifecycle support of medical device software, including software incorporating artificial ...
... of engineering of considerable scope and complexity. May also perform as a technical staff ... D with five years previous related experience. • Extensive knowledge of the medical device ...
... of engineering of considerable scope and complexity. May also perform as a technical staff ... D with five years previous related experience. • Extensive knowledge of the medical device ...
Bachelor's degree in Engineering ... Demonstrated experience leading medical device manufacturing and/or NPD teams What else you'll need ...
Bachelor's degree in Engineering ... Demonstrated experience leading medical device manufacturing and/or NPD teams What else you'll need ...
Bachelor's degree in Engineering ... Demonstrated experience leading medical device manufacturing and/or NPD teams What else you'll need ...
Bachelor's degree in Engineering ... Demonstrated experience leading medical device manufacturing and/or NPD teams What else you'll need ...
Firmware / Backend Software Engineer Gynesis Platform -- Neuromodulation Business Unit **on-site in ... Experience with medical device software developed under IEC 62304, including cybersecurity and FDA ...
Quick apply
Firmware / Backend Software Engineer Gynesis Platform -- Neuromodulation Business Unit **on-site in ... Experience with medical device software developed under IEC 62304, including cybersecurity and FDA ...
Quality Engineer II - Process Engineering
Salt Lake City, UT · On-site
$69K - $90K/yr
Medical device industry experience. * Hands-on NCR authoring experience, including investigation, disposition, root cause analysis, corrective action, and documentation closure. * Keyence programming ...
Quality Engineer II - Process Engineering
Salt Lake City, UT · On-site
$69K - $90K/yr
Medical device industry experience. * Hands-on NCR authoring experience, including investigation, disposition, root cause analysis, corrective action, and documentation closure. * Keyence programming ...
Intern Medical Device Engineer information
What is the difference between Intern Medical Device Engineer vs Junior Medical Device Engineer?
| Aspect | Intern Medical Device Engineer | Junior Medical Device Engineer |
|---|---|---|
| Credentials | Typically pursuing or recently completed a relevant degree | Bachelor's or Master's in biomedical, mechanical, or related engineering |
| Work Environment | Internship setting, supervised, learning-focused | Entry-level professional role, more independent tasks |
| Employer & Industry Usage | Medical device companies, research labs, internships | Medical device companies, manufacturing, R&D teams |
Intern Medical Device Engineers are usually students or recent graduates gaining hands-on experience, while Junior Medical Device Engineers are entry-level professionals with some work experience. The internship focuses on learning and support, whereas the junior role involves more responsibility in product development and testing.
What types of projects and responsibilities can an intern medical device engineer expect during their internship?
What does an intern medical device engineer do?
What are the key skills and qualifications needed to thrive as an intern medical device engineer?
Full-time
Posted 4 days ago
Job description
Position Summary
We are seeking an industry-leading extrusion expert to serve as a Principal Process Development Engineer (PPDE) and Subject Matter Expert (SME) for extrusion technologies across our manufacturing sites. This role will be responsible for establishing and institutionalizing best-in-class process development standards, guidelines, and technical frameworks for a wide range of extrusion processes used in medical device manufacturing.
The ideal candidate will bring deep technical expertise, a track record of innovation, and the ability to elevate organizational capability through knowledge-based process development, standardization, and cross-site collaboration.
Key Responsibilities
Technical Leadership & SME Role
- Serve as the enterprise-wide technical authority on extrusion processes (e.g., single-lumen, multi-lumen, co-extrusion, and micro-extrusion).
- Provide expert guidance in solving complex process challenges, including material behavior, tooling design, and process optimization.
- Lead root cause investigations and corrective actions for critical extrusion-related issues.
Process Development Standards & Frameworks
- Develop and deploy standardized process development methodologies aligned with scientific/knowledge-based engineering principles.
- Establish process characterization protocols, DOE, and validation approaches (IQ/OQ/PQ).
- Create design guidelines for tooling, die design, and downstream equipment integration.
- Define critical process parameters (CPPs) and control strategies.
Technology Development & Innovation
- Identify and drive adoption of advanced extrusion technologies, including micro-extrusion and multi-material extrusion.
- Lead feasibility studies for new materials (e.g., implantable polymers such as PEEK, TPU, PCU).
- Evaluate and recommend new equipment, automation, and digital process monitoring solutions.
Cross-Functional & Cross-Site Collaboration
- Partner with Product Development, Operations, Quality, and Application Development teams.
- Ensure smooth technology transfer from development to production across sites.
- Standardize best practices across extrusion plants to ensure consistency and scalability.
Capability Building & Mentorship
- Mentor Process Development Engineers and Technicians in extrusion science and engineering.
- Develop and deliver training programs and technical documentation.
- Build organizational competency in extrusion process development and validation.
Quality & Compliance
- Ensure all processes meet regulatory requirements (FDA, ISO 13485) and internal quality standards.
- Support validation strategies for Class II and Class III medical device components.
- Integrate SPC, digital quality systems, and Industry 4.0 tools (IIoT) into extrusion processes.
Education
- Bachelor’s degree in Plastics Engineering or Polymer Engineering or Mechanical Engineering (M.S, Ph.D. preferred)
Experience
- 15+ years of hands-on experience in extrusion process development, preferably in medical device manufacturing.
- Demonstrated expertise in:
- Micro-extrusion and tight-tolerance tubing
- Multi-lumen and co-extrusion processes
- Processing of advanced polymers (e.g., PEEK, TPU)
- Proven track record of developing and implementing process standards and scalable solutions across multiple sites.
Technical Skills
- Strong understanding of:
- Polymer rheology and material science
- Tooling/die design and flow dynamics
- Scientific extrusion principles and DOE methodologies
- Experience with process monitoring, automation, and data analytics tools.
Preferred Qualifications
- Experience in medical-grade thermoplastic materials.
- Experience integrating digital manufacturing / IIoT systems into extrusion processes.
- Experience with additional polymer processing techniques preferred.
About Spectrum Plastics Group
Sourced by ZipRecruiter
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Alpharetta, GA, US
Year founded
1961