Process Engineer

Hello,

I hope you're doing well.

My name is Mahalakshmi, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for Process Engineer based Tempe, Arizona (On-Site), at one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at

mahalakshmi.n@intellectt.com

Experience: 3 7 Years (Preferred) Industry: Medical Device Manufacturing Department: Manufacturing / Process Engineering

Position Summary

We are seeking a Process Engineer to develop, validate, optimize, and maintain manufacturing processes used in the production of medical devices and components.

The ideal candidate will have experience in medical device manufacturing processes, process validation, statistical analysis, continuous improvement, and manufacturing troubleshooting.

Key Responsibilities

• Develop and optimize manufacturing processes for medical device production.
• Support automated assembly, injection molding, bonding, welding, or other device manufacturing operations as applicable.
• Develop process specifications, manufacturing procedures, and equipment operating parameters.
• Execute process validation activities, including IQ/OQ/PQ and supporting documentation.
• Conduct process capability studies, statistical analysis, and DOE activities.
• Perform root cause analysis for manufacturing defects, scrap, and process deviations.
• Collaborate with Quality Engineering to support CAPA, nonconformance investigations, and change control.
• Implement Lean Manufacturing and Six Sigma process improvement initiatives.
• Support new product introduction, manufacturing scale-up, and process transfers.
• Develop and maintain process FMEAs, control plans, and work instructions.
• Monitor production yield, cycle time, process stability, and manufacturing performance.

Required Qualifications

• Bachelor's degree in Mechanical, Manufacturing, Industrial, Biomedical, Chemical Engineering, or a related discipline.
• 3+ years of manufacturing process engineering experience.
• Experience in FDA-regulated medical device manufacturing preferred.
• Hands-on experience in manufacturing process validation and IQ/OQ/PQ.
• Knowledge of statistical process control, DOE, process capability analysis, and Minitab.
• Familiarity with ISO 13485, FDA QMSR, and applicable medical device quality requirements.
• Strong troubleshooting, technical writing, and process improvement capabilities.

Key Skills: Process Engineering, IQ/OQ/PQ, Process Validation, Minitab, DOE, SPC, PFMEA, CAPA, Manufacturing Process Optimization, ISO 13485.

Benefits: Eligible employees may have access to benefits offered by Intellectt Inc. in accordance with the applicable benefit plans and eligibility requirements.

Equal Employment Opportunity:
Intellectt Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local law.

Thanks & Regards,
Mahalakshmi
Junior Recruiter
Intellectt Inc

mahalakshmi.n@intellectt.com