Product Development Specialist (El Paso)
Stellar Consulting Solutions, LLC, El Paso, TX, United States
• Role
Product Development
• Location:
: El Paso Texas 79912, Onsite
• Experience: 5+ Years
We’re looking for a hands-on engineer to support product development and new product transfer into manufacturing within a GMP-regulated environment (Medical Device / Pharma).
If you have strong experience in validation, process development, and risk management, this could be a great fit.
Key Responsibilities
• Lead/support new product development & transfers (NPI)
• Develop and execute IQ/OQ/PQ validation protocols
• Perform FMEA (risk management)
• Drive process characterization & DOE (Design of Experiments)
• Create SOPs, validation documentation & manufacturing procedures
• Support equipment/tooling, installation & supplier coordination
• Ensure compliance with GMP / ISO standards
Must-Have Experience
• 5+ years in manufacturing / process / product development
• Strong hands-on experience with IQ/OQ/PQ validation
• Experience with FMEA and GD&T
• Background in medical device or pharmaceutical industry
• Experience working in GMP / regulated environments
• Strong technical documentation skills
Nice to Have
• DOE / Minitab experience
• CAD tools (SolidWorks, AutoCAD)
• Lean Six Sigma or Project Management certification
Product Development
• Location:
: El Paso Texas 79912, Onsite
• Experience: 5+ Years
We’re looking for a hands-on engineer to support product development and new product transfer into manufacturing within a GMP-regulated environment (Medical Device / Pharma).
If you have strong experience in validation, process development, and risk management, this could be a great fit.
Key Responsibilities
• Lead/support new product development & transfers (NPI)
• Develop and execute IQ/OQ/PQ validation protocols
• Perform FMEA (risk management)
• Drive process characterization & DOE (Design of Experiments)
• Create SOPs, validation documentation & manufacturing procedures
• Support equipment/tooling, installation & supplier coordination
• Ensure compliance with GMP / ISO standards
Must-Have Experience
• 5+ years in manufacturing / process / product development
• Strong hands-on experience with IQ/OQ/PQ validation
• Experience with FMEA and GD&T
• Background in medical device or pharmaceutical industry
• Experience working in GMP / regulated environments
• Strong technical documentation skills
Nice to Have
• DOE / Minitab experience
• CAD tools (SolidWorks, AutoCAD)
• Lean Six Sigma or Project Management certification