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Locum Medical Device Design Jobs (NOW HIRING)

Imh

Apply knowledge of medical device design and 3D visualization (XR and Spatial Computing) and 3D printing technologies and associated postprocessing techniques and tools, in delivering the Advanced ...

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... design specification requirements * Generate Quality System Records on applicable ACIST/BMT ...

ICU Medical

Senior Engineer, R&D

Salt Lake City, UT · On-site

$101K - $138K/yr

The ideal candidate will bring extensive hands-on experience in medical device design and development, with a strong background in documentation, testing, and risk management. Essential Duties ...

ICU Medical

Senior Engineer, R&D

Salt Lake City, UT

$101K - $138K/yr

The ideal candidate will bring extensive hands-on experience in medical device design and development, with a strong background in documentation, testing, and risk management. Essential Duties ...

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... design specification requirements * Generate Quality System Records on applicable ACIST/BMT ...

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Locum Medical Device Design information

What are some common challenges faced by locum medical device design professionals when integrating into new teams and projects?

Locum medical device design professionals often face the challenge of quickly adapting to new team dynamics and project workflows. Since projects may be at various stages of development, locums must rapidly familiarize themselves with existing designs, documentation, and regulatory requirements. Effective communication and collaboration with both engineering and clinical teams are crucial to ensure seamless integration and contribute to project goals. Flexibility and a proactive approach to learning company-specific processes can help locums succeed in these dynamic environments.

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

To thrive as a Locum Medical Device Designer, you need a solid background in biomedical engineering, product design, and regulatory standards, often supported by a relevant degree and prior experience in device development. Familiarity with CAD software, rapid prototyping tools, and knowledge of FDA or CE compliance processes are typically required. Strong problem-solving, adaptability, and effective collaboration skills help individuals excel in varied project environments and short-term assignments. These competencies ensure the delivery of innovative, compliant, and user-centered medical devices within tight timelines.

What is the difference between Locum Medical Device Design vs Contract Medical Device Engineer?

AspectLocum Medical Device DesignContract Medical Device Engineer
CredentialsRelevant engineering degrees, certifications in medical device designSame as locum, often with specialized certifications
Work EnvironmentTemporary assignments in various companies or projectsProject-based, often in corporate or manufacturing settings
Employer & Industry UsageUsed by staffing agencies, hospitals, and medical device firmsEngaged by companies for specific projects or product development

Both roles involve designing medical devices, requiring similar credentials and working in related environments. The key difference is that a locum medical device designer works temporarily across different organizations, while a contract medical device engineer is typically hired for specific projects within a single company.

What are locum medical device design professionals?

Locum medical device design professionals are experts who temporarily fill roles in the design and development of medical devices, often to cover staff shortages or support specific projects. They bring specialized knowledge in engineering, regulatory compliance, and product development, and may be involved in tasks such as prototyping, testing, and documentation. These professionals help companies maintain productivity and meet deadlines without the commitment of a permanent hire. The locum arrangement offers flexibility for both the employer and the professional, and is common in industries requiring highly specialized skills.
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Locum Medical Device Design jobs near you

Test Engineer - Verification & Validation - medical device

InnoTech Staffing

Manchester, NH • On-site

Full-time

Posted 2 days ago

Job description

InnoTECH Staffing has an immediate opening for a Test Engineer to work in a dynamic medical device R&D environment at our client who is located in Manchester, NH.

This requires being onsite 5 days a week and must be a US Citizen or Greencard holder.

Test Engineering is a high-visibility role with a significant, direct impact on the success of the project.
How you will make an impact as a Verification and Validation Test Engineer:

  • Developing and writing test procedures assessing end-to-end performance and reliability of user interfaces and hardware
  • Understanding device design and core technologies in order to inform test method development
  • Determining test coverage for revisions to design
  • Creating and evaluating test fixtures if needed for product design verification
  • Contributing to design failure investigations that may impact Risk Assessments, Hazard Analyses, and FMEAs
  • Contributing toward regulatory and agency submissions
  • Authoring Test Summaries and other documents

To be successful in this role as a Verification and Validation Test Engineer, you will need the following skills and experience:

  • Must have a BS in Physics, Biology, Electrical, Mechanical, or Biomedical Engineering.
  • Experience with research, development, and product testing
  • Experience writing procedures for others to follow
  • Experience with data and failure analysis
  • Broad measurement instrument knowledge
  • Knowledge and deep understanding of engineering fundamentals
  • Demonstrated problem solving ability and techniques
  • Ability to work as part of an interdisciplinary team
  • Self-motivated and able to self-prioritize
  • Ability to clearly explain objectives
  • Must be detail oriented and have excellent verbal and written communication skills
  • Experience in medical devices, knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred