Assistant Process Engineer

Net2Source (N2S); Harvard (MA); On-site; USD 38,572 - 40,294; Full time

Job summary

A leading process engineering company is seeking an Assistant Process Engineer at its Devens Cell Therapy Facility in Massachusetts. This role involves assessing process-related deviations, analyzing performance data, and providing technical support to cross-functional teams. Candidates should hold a Bachelor's degree in Science or Chemical/Biological Engineering and have proficiency in Excel and JMP. This position offers opportunities for growth in trend investigations and continuous improvement in a collaborative work environment.

Qualifications

• Bachelor's degree in Science or Chemical/Biological Engineering required.
• Minimum of 0–2 years of industry experience, preferably in cGMP or Cell Therapy manufacturing.
• Proficiency in Excel and JMP for data analysis is essential.

Responsibilities

• Assess process-related deviations and provide data-driven evaluations.
• Analyze performance data to identify improvement opportunities.
• Verify data accuracy across multiple GMP systems.
• Provide technical support for equipment and process-related issues.
• Collaborate with cross-functional teams on processes.

Skills

Proficiency in Excel

Proficiency in JMP

Strong presentation skills

Strong communication skills

Strong problem-solving skills

Troubleshooting skills

Education

Bachelor’s degree in Science or Chemical/Biological Engineering

Tools

Tableau

Spartan

Mareana

Job description

Job Title

Assistant Process Engineer

Duration

06+ Months (Extendable)

Pay Rate

$28.00 – $29.25/hr on W2

Must Haves

• Proficiency in Excel and JMP for data analysis
• Familiarity with GMP documentation and electronic data systems.

Position Summary

Associate Process Engineer role is based at Devens Cell Therapy Facility (CTF). This role is responsible for assessing process-related deviations, analyzing performance data to identify trends and improvement opportunities, and providing technical support to cross-functional teams. The position requires proficiency with data monitoring and analysis tools, strong presentation and communication skills, and the ability to verify data accuracy across multiple GMP systems. Additional duties include assisting in deviation prevention and closure, applying continuous improvement tools, and performing gowning activities to enter manufacturing areas.

Key Responsibilities

• 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 received from the manufacturing floor to identify problem areas with the process and recommend solutions.
• Summarize and present findings effectively to audiences with varying levels of technical understanding; strong presentation and communication skills are essential.
• Verify data accuracy across multiple GMP systems; maintain strong understanding of GMP data systems and move swiftly between platforms.
• Provide on-the-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.
• Perform gowning activities and enter manufacturing areas as needed.
• This position offers growth opportunities to expand into trend investigations using statistical tools (e.g., EWMA, control charts) and evaluating manufacturing capabilities for continuous improvement.

Basic Qualifications

• Required Bachelor’s degree in Science or Chemical/Biological Engineering.
• Minimum 0–2 years of industry experience; cGMP or Cell Therapy manufacturing experience preferred.
• Proficiency in Excel and JMP for data analysis.

Preferred Skills

• Experience with Tableau, Spartan, and Mareana is a plus.
• 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.

Working Conditions

• Office-based role with occasional entry into GMP manufacturing areas.
• Ability to perform gowning activities and comply with cleanroom requirements.
• Exposure to strong magnetic fields and hazardous materials in manufacturing areas.

Location

Devens, MA