Assistant Process Engineer

The Senior Specialist participates in facility, process, and aseptic validation activities, including support of the Aseptic Process Simulation Program and implementation of process lifecycle management changes. Education/Experience/ Licenses/Certifications Knowledge of science generally attained through studies resulting in a Bachelor’s degree in science, engineering, biochemistry or related discipline, is required.

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Net2Source Inc. isn’t just another staffing company, we’re a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price.

Job Title: Assistant Process Engineer
Work Location: 50% onsite at Devens, MA 01434
Duration: 06+ Months (Extendable)
 
Pay Rate: $32.00 - 34.42/hr on W2
 

Name Required Experience Excellent Technical Writing Skills Yes 0-2 yrs   Aseptic Techniques and Processes No 0-2 yrs   clean room gowning No 0-2 yrs

 
Must Haves:
Bachelor's degree required
Experience in Technical writing such as SOPs, protocols, summary reports and/or change controls.
 
Description:
The Senior Specialist, MS&T Validation provides process validation support to the Devens Cell Therapy Facility (CTF). The Senior Specialist participates in facility, process, and aseptic validation activities, including support of the Aseptic Process Simulation Program and implementation of process lifecycle management changes.
 
Job Responsibilities:

• Responsible for oversight of CTF Process Validation activities including, but not limited to Aseptic Process Simulations/ Validations (APS/APV), and other Lifecycle Management changes.
• Prepares written protocols/reports/summaries supporting validation studies.
• Ensures safe and compliant cGMP operations, maintains permanent inspection readiness.
• This position reports to the Associate Director of Manufacturing Science and Technology Validation.

 
Specific Knowledge, Skills, Abilities:

• Experience in cGMP’s and multi-national biopharmaceutical/cell therapy regulations
• Excellent verbal/written communication skills

 
Education/Experience/ Licenses/Certifications

• Knowledge of science generally attained through studies resulting in a Bachelor’s degree in science, engineering, biochemistry or related discipline, is required
• A minimum of 2 years’ experience in biopharmaceutical operations, or its equivalent is required.

Why Work With Us?
We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter.
Our Commitment to Inclusion & Equity
Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.
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• America’s Most Honored Businesses (Top 10%)
• Fastest-Growing Staffing Firm by Staffing Industry Analysts
• INC 5000 List for Eight Consecutive Years
• Top 100 by Dallas Business Journal
• Spirit of Alliance Award by Agile1
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