×
Register Here to Apply for Jobs or Post Jobs. X

Assistant Process Engineer - MSAT

Job in Northern, Floyd County, Kentucky, USA
Listing for: Sokolservices
Full Time position
Listed on 2026-10-13
Job specializations:
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 27 - 29 USD Hourly USD 27.00 29.00 HOUR
Job Description & How to Apply Below

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.

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.
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.
  • 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.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary