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Product Development Engineer - Urgent Need (Onsite)

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Onsite

Product Development Engineer - Urgent Need (Onsite)

MillenniumSoft Inc

Product Development Engineer - Urgent Need (Onsite)

Skills

RData AnalysisCompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

El Paso, TX, USA

Work mode:

Onsite

Published on:

22 August 2026

What they need


Position : Product Development Engineer 1 Location : El Paso, TX Duration : 12 Months **Total Hours/week : 40.00

pay range -$25-30/hr** 1st Shift Client : Medical Devices Company Job Category : Engineering Level of Experience : Entry Level Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT Job Description

  • Support technical and/or cross-functional project work to further design and development activities for new and existing products.
  • Apply engineering fundamentals, concepts and practices to advance new product development efforts.
  • Demonstrate basic understanding of design control process.
  • Develop raw material and in-process inspection test methods as well as test method validation (i.e., MSA, Gage R&R).
  • Support installation and qualification of R&D equipment.
  • Perform data analysis and write technical reports based on product design activities.
  • Demonstrated ability to utilize statistical tools and computer analysis.
  • Support purchasing process of materials, equipment and testing consumables.
  • Ensure compliance with client quality policies, procedures and practices as well as with all local, state, federal and client safety regulations, policies and procedures.
  • Personal leadership, team player, innovation/risk taker, results oriented, integrity, interpersonal skills, technical skills
  • Able to adapt to shifting priorities and work in a fast-paced environment
  • Comfortable with ambiguity and able to make progress in the face of uncertainty.
  • BS degree in engineering is required (Mechanical or Biomedical Engineering preferred).
  • 1-2 years of engineering experience is required, preferably in FDA regulated environment.
  • 1-2 years of acquaintance with cGMP's (21CFR211), 21CFR820 and ISO13485.

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