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EMC & Product Safety Electrical Engineer – R&D (Medical Devices)

Collabera

Princeton (NJ)

On-site

USD 40,000 - 45,000

Full time

Yesterday
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Job summary

Collabera is seeking a skilled Electrical Engineer to work on R&D of electro-mechanical medical devices in Princeton, NJ. This role involves designing mixed-signal circuits, ensuring product safety compliance, and documenting strategies per regulatory standards. Ideal candidates have significant experience in circuit design and familiarity with certification processes.

Qualifications

  • 5-8 years’ experience in circuit design and EMC testing.
  • Proficiency in Electrical Engineering tools is required.
  • Strong understanding of FDA-regulated environments.

Responsibilities

  • Lead R&D activities across the product lifecycle.
  • Develop EMC and Product Safety strategies.
  • Collaborate with cross-functional teams.

Skills

Problem-solving
Documentation skills
Communication

Education

Bachelor’s degree in Electrical Engineering or related field

Tools

ORCAD Capture
PSpice
Mentor Graphics PADS

Job description

EMC & Product Safety Electrical Engineer – R&D (Medical Devices)

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Collabera provided pay range

This range is provided by Collabera. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$40.00/hr - $45.00/hr

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We are seeking a skilled Electrical Engineer with hands-on experience in R&D of electro-mechanical medical devices. The ideal candidate will have expertise in mixed-signal analog/digital circuit design, EMC and product safety compliance, and cross-functional product development.

Key Responsibilities:

  • Lead and support R&D activities across full product lifecycle – from feasibility and prototyping to system-level design.
  • Design and analyze mixed-signal circuits for medical device applications.
  • Develop EMC and Product Safety strategies and documentation for new and existing products in alignment with applicable standards (IEC/EN 61326-1/2-6, UL/IEC 61010, 60950/62368-1).
  • Author and execute EMC test plans and reports; conduct troubleshooting and root cause analysis.
  • Interface with external certifying bodies (UL, CE, CB Scheme) to ensure product compliance.
  • Support validation activities, including protocol/report generation and execution (V&V, CAPA).
  • Provide technical guidance on design changes related to EMC/Safety impacts.
  • Maintain and operate EMC/Safety testing equipment; write equipment SOPs.
  • Collaborate closely with electrical, mechanical, and quality engineering teams.

Qualifications:

Required:

  • Bachelor’s degree in Electrical Engineering or related field (or equivalent combination of education and technical experience).
  • 5–8 years’ experience in circuit design, product safety, and EMC testing in a regulated environment.
  • Proficiency in tools such as ORCAD Capture, PSpice, and Mentor Graphics PADS.
  • Strong understanding of EMC/Safety standards, FDA-regulated product environments, and IVD device compliance.

Preferred:

  • Bachelor's in Electrical, Biomedical Engineering, or Physics.
  • Experience interfacing with certification agencies.
  • Familiarity with UL file maintenance, CE Technical Files, and FDA quality systems.

Skills & Attributes:

  • Strong problem-solving and documentation skills.
  • High level of integrity, collaboration, and adaptability.
  • Excellent verbal/written communication and attention to detail.
  • Ability to lead and contribute within cross-functional teams.
Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Contract
Job function
  • Job function
    Engineering and Science
  • Industries
    Medical Equipment Manufacturing, Biotechnology Research, and Pharmaceutical Manufacturing

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