Assistant Process Engineer

This range is provided by TSR Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$28.00/hr - $29.00/hr

*** Please only local candidates to Devens, MA 84079

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.

Our client, a leading pharmaceutical company, is hiring an Assistant Process Engineer for a 6+ month contracting assignment.

• Familiarity with GMP documentation and electronic data systems
• Proficiency in Excel and JMP for data analysis
• Bachelor’s degree in Science or Chemical/Biological Engineering (preferred)
• Minimum 0–2 years of industry experience; cGMP or Cell Therapy manufacturing experience preferred

• Experience with Tableau, Spartan, and Mareana
• Strong technical understanding of cell therapy manufacturing processes
• Familiarity with GMP documentation and electronic data systems
• Technical writing skills for authoring impact assessments, SOPs, and clear documentation
• Ability to work collaboratively in a fast‑paced environment
• Strong problem‑solving, troubleshooting, and presentation skills

• Assess process‑related deviations, analyze performance data to identify trends and improvement opportunities, and provide technical support to cross‑functional teams
• Proficiency with data monitoring and analysis tools and verifying data accuracy across multiple GMP systems
• Assist in deviation prevention and closure, apply continuous improvement tools, and perform gowning activities to enter manufacturing areas
• Assess the impact of process‑related deviations and provide clear, data‑driven evaluations
• Analyze process performance data to identify trends and improvement opportunities; experience with data monitoring systems such as Tableau, Spartan, and Mareana is a plus, as well as proficiency in Excel and JMP for data analysis
• Assess trends in support calls from the manufacturing floor, identify problem areas, and recommend solutions
• Summarize and present findings effectively to audiences with varying levels of technical understanding
• Verify data accuracy across multiple GMP systems; maintain a strong understanding of GMP data systems and move swiftly between platforms
• Provide on‑floor technical support for equipment and process‑related issues
• Assist in deviation prevention and closure through site quality systems
• Collaborate with cross‑functional teams including Scheduling, MSAT, Supply Chain, Quality, and Facilities & Engineering
• Apply continuous improvement tools to identify and close procedural and compliance gaps

6+ month contracting assignment.

Employment type:

Contract.

Associate

Other – Pharmaceutical Manufacturing

• Medical insurance
• 401(k)