Senior Process Engineer

Senior Process Engineer

Location:

Tempe, AZ, USA (85285). Work model:
Hybrid (4 days onsite).

Shift: 8am-5pm, Monday-Friday.

Employment type:

Temporary, full-time, 6 months. Hourly rate: $66.00–$69.00.

Senior Process Engineer with experience in regulated manufacturing environments including process validation, equipment selection, and GMP-compliant project execution.

• Bachelor's Degree in Engineering

• Bachelor's Degree in Industrial Engineering or Systems Engineering

• 2+ years of relevant engineering experience
• Strong understanding of manufacturing processes and product development
• Experience supporting process improvements and manufacturing operations
• Ability to analyze equipment performance and conduct testing
• Knowledge of GMP and workplace safety requirements
• Strong communication and cross‑functional collaboration skills

• Lean Six Sigma Green Belt certification or higher
• Knowledge of manufacturing processes, materials, products, and process design
• Understanding of Design for Manufacturing (DFM), statistical tools, and validation techniques
• Experience writing and executing validations
• Experience in New Product Introduction (NPI) or Manufacturing Engineering
• Experience in FDA-regulated or other regulated industries
• Experience with PFMEA, Control Plans, SOPs, PPAP, MSA, and capability studies

• Support new product and process introductions in accordance with company procedures
• Ensure product and process quality meet operational and material specifications
• Assist with equipment selection, design, installation, qualification, and validation
• Support capital equipment acquisition activities and vendor coordination
• Develop operations, troubleshooting, and maintenance documentation
• Analyze equipment performance and conduct experimental testing
• Drive process improvements to reduce time‑to‑market while meeting regulatory and cost requirements
• Participate in process reviews, PFMEA activities, and production launch efforts
• Conduct capability studies, validations, qualifications, and MSA activities
• Review and approve validation documentation
• Provide hands‑on manufacturing floor support for new process implementation
• Communicate project updates and collaborate with cross‑functional stakeholders
• Train manufacturing personnel on new processes and procedures
• Ensure compliance with GMP, safety, and regulatory requirements

For information and details on employment benefits offered with this position, please visit our HR portal.

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E‑Verify). (Posting required by OCGA 13/10‑91).

Only those lawfully authorized to work in the designated country associated with the position will be considered.