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Product Development Engineer

Job in El Paso, El Paso County, Texas, 88568, USA
Listing for: Millenniumsoft, Inc
Full Time position
Listed on 2026-08-07
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 30 - 40 USD Hourly USD 30.00 40.00 HOUR
Job Description & How to Apply Below

Position :
Product Development Engineer 1

Location :
El Paso, TX

Duration : 12 Months

Total Hours/week : 40.00

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

$35/hr

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 (21

    CFR
    211), 21

    CFR
    820 and ISO
    13485.
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