Engineering Specialist

Mirion Technologies JobsNorfolk, VA
8hOnsite

About The Position

The Engineering Specialist I supports the design, development, and integration of medical device products, including new product introductions (NPI) and sustaining engineering for legacy systems. This entry level role is ideal for candidates with a background in mechanical, biomedical, or electrical engineering and an interest in medical device manufacture and associated analysis software. Familiarity with medical physics including medical device imaging and analysis (CT, MRI, X-Ray) is a plus. The position emphasizes hands-on technical work, documentation, and collaboration with cross-functional teams in a regulated environment. This role is fully on-site. Only applicants who do not require Visa sponsorship will be considered for this role.

Requirements

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or Electrical Engineering.
  • 0–2 years of engineering experience (internships or co-op experience preferred).
  • Strong attention to detail, organizational skills, and ability to learn quickly.
  • Effective communication and teamwork skills.
  • Ability to learn and adapt in a fast-paced environment to meet all deliverables including safety, cost, and milestone dates
  • Problem-solving mindset and willingness to take initiative.
  • Commitment to quality and regulatory compliance.

Nice To Haves

  • Understanding of medical manufacturing processes or software integration is a plus.
  • Familiarity with CAD tools (e.g., SolidWorks) andProduct Lifecycle Management (PLM) tools.
  • Knowledge of of Enterprise Resource Programs (ERP systems) is a plus.
  • Experience in mechanical, electrical or software design is a plus.

Responsibilities

  • Assist in new product development and introduction (NPI) activities: o Support concept generation, design, prototyping, and testing. o Participate in risk assessment, verification, and validation tasks. o Help prepare design documentation in compliance with ISO and FDA standards.
  • Collaborate with other engineers, Operations’ Management and Associates, and other key departments to ensure design feasibility and smooth production transition.
  • Conduct basic experiments and feasibility studies under guidance.
  • Provide technical support and troubleshooting To improve production quality and foster continuous improvement.
  • Maintain accurate records and contribute to continuous improvement initiatives.
  • Create and revise engineering data in our Enterprise Management Program to ensure accurate and efficient product manufacturing and quality control.
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