Product Development Engineer 1
MillenniumSoft Inc
Date: 11 hours ago
City: El Paso, TX
Contract type: Full time
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
Job Description
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
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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