Assistant Process Engineer - MSAT
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Before you apply
Salary$27 – $29/hr
LocationDevens, Massachusetts, United States
Work modehybrid
Typecontract
SeniorityEntry
ExperienceUp to 2 yrs
Company size11+ people
PostedOct 9, 2026 · 3w ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
Bachelor's degree in Chemical Engineering, Biochemical Engineering, Chemistry, or a related technical discipline
0-2 years of industry experience
Strong GMP experience within an industry environment
cGMP or Cell Therapy manufacturing experience
Technical writing skills for authoring impact assessments and Out-of-Specification investigations
Strong problem-solving, troubleshooting, and presentation skills
Familiarity with GMP documentation and electronic data systems
Strong analytical and critical-thinking skills with attention to detail
Ability to work collaboratively in a fast-paced environment
Effective communication skills with the ability to work cross-functionally with Quality, Manufacturing, and Engineering stakeholders
Pharmaceutical or biopharmaceutical industry background
Strong technical understanding of cell therapy manufacturing processes
Authorization to work in the United States without visa sponsorship
Benefits
Health insurance
Dental insurance
Vision insurance
Holiday pay
401(k)
Employee referral bonus program
About the role
The Junior MSAT Process Engineer will support Manufacturing Science and Technology activities with a primary focus on Out-of-Specification (OOS) investigations within a GMP-regulated manufacturing environment.
Responsibilities
The role will support OOS investigations by reviewing batch records, process data, equipment logs, and analytical results and helping develop technically sound investigation findings and conclusions. Investigation ownership may be assigned as appropriate.
The engineer will work cross-functionally with Quality Assurance, Quality Control, Manufacturing, and Engineering to gather data, align on investigation scope, and present investigation findings and technical rationale to cross-functional teams and management.
Strong GMP experience is important for this position. Pharmaceutical or biopharmaceutical industry experience is preferred.
Position details:
• Hourly rate: $27.30–$29.30;
• Start date: October 19, 2026;
• Contract length: 6 months with possible extension;
• Location: Devens, MA 01434;
• Work arrangement: Hybrid, minimum 50% onsite;
• Schedule: Monday–Friday, normal business hours;
• Maximum hours: 40 hours per week;
• W-2 contract position;
• No C2C options;
• No visa sponsorship.
Requirements
Required:
• Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Chemistry, or a related technical discipline;
• 0–2 years of industry experience;
• Strong GMP experience within an industry environment;
• cGMP or Cell Therapy manufacturing experience;
• Technical writing skills for authoring impact assessments and Out-of-Specification investigations;
• Strong problem-solving, troubleshooting, and presentation skills;
• Familiarity with GMP documentation and electronic data systems;
• Strong analytical and critical-thinking skills with attention to detail;
• Ability to work collaboratively in a fast-paced environment;
• Effective communication skills with the ability to work cross-functionally with Quality, Manufacturing, and Engineering stakeholders;
• Authorization to work in the United States without visa sponsorship.
Preferred:
• Pharmaceutical or biopharmaceutical industry background;
• Strong technical understanding of cell therapy manufacturing processes.
Benefits
•
Health insurance with dental and vision insurance options.
•
Holiday pay.
•
401(k) program.
•
Employee referral bonus program.
•
The client retains the right to hire the contractor directly.