Product Development Engineer/GIE EPI Engineer
Job in
El Paso, El Paso County, Texas, 79912, USA
Listed on 2026-06-01
Listing for:
Sunrise Systems Inc
Contract
position Listed on 2026-06-01
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering, Process Engineer, Mechanical Engineer
Job Description & How to Apply Below
Our client, a leading Medical Device Manufacturing Company is looking for Product Development Engineer 3 / GIE EPI Engineer 3 and This is for an initial duration of 12 Months Contract – El Paso, TX
Job Title:
Product Development Engineer 3 / GIE EPI Engineer 3
Job
-02521
Location:
El Paso, TX
Duration: 12 Months Contract
Position Type:
Hourly Contract Position (W2 only)
- GIE EPI Contractor Engineer 3
- On site 5 days a week.
- Education bachelor's degree
Summary of Position with General Responsibilities:
- Leads technical support to new product transfers and/or product development projects.
- Possesses technical responsibility for interpreting, planning, organizing, executing, coordinating, and carrying out technical assignments based on diversified requirements.
Technical Skills
Must Have
- Risk Management:
Experience with FMEA (Failure Mode and Effects Analysis) - Technical Documentation:
Experience developing SOPs, validation protocols and process documentation - understanding Geometric Dimensioning and Tolerancing (GD&T)
- Validation Protocols:
Development and execution of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)
- CAD/CAM software (Solid Works, AutoCAD)
Essential Job Functions:
- Coordinates and Supports Suppliers for Manufacturing of Custom Equipment/Tooling
- Coordinates purchase and delivery of Equipment/Tooling
- Coordinates installation of Equipment/Tooling
- Develops and Executes IQ and OQ Protocols and Reports
- Develops and Executes Test Method Validations / Gage R&R
- Generates and Issues for Approval SOPs and Manufacturing Procedures
- Develops and Executes Component Qualifications
- Develops and Executes PQ and PPQ Protocols and Reports
- Develops Manufacturing Capacity Analysis
- Develops and Executes Process Characterizations / Design of Experiments (DOE)
- Develops documentation/justification for assigned capital projects
- Complies with cGMP's, Quality Standards , and established policies and procedures
- Executes other duties assigned by his supervisor
Basic Qualifications:
- Bilingual - English and Spanish (oral and written)
- Technical writing skills
- GMP, ISO, EHS and Statistical regulations knowledge
- Strong Computer Skills/Knowledge (Word, Excel, PowerPoint)
- MS Project knowledge
- Minitab Proficiency
Additional Desirable Qualifications Skills and Knowledge:
- Lean / Six sigma Training/Certification
- Project Management Training/Certification
- Engineering Board Certification (EIT / PE)
Education and/or Experience:
- Bachelor's Degree in Engineering
- Experience in the Medical Device / Pharmaceutical Industries:
Yes - 5+ years of experience in the following fields:
- Manufacturing
- New Product Transfers
- Product / Process Development
Job Functions Experience in the following:
- Qualification / Validation (IQ/OQ/PQ)
- Test Method Validation / Gage R&R
- Process Characterization / Design of Experiments (DOE)
- Manufacturing Line Design / Capacity Analysis
- Equipment / Tooling Design
- Equipment Installation / Preventive Maintenance Procedure Generation
- Root Cause Analysis / Investigation
- SOP / Manufacturing Procedures Generation & Change Control
- Product Financials & Supply Chain Structure Design
- OEE Integration, Vertical Start up and Zero-loss mindset
Thank You
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