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Process Engineer

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Barrington James
Full Time position
Listed on 2026-03-09
Job specializations:
  • Engineering
    Manufacturing Engineer, Process Engineer, Validation Engineer, Quality Engineering
  • Manufacturing / Production
    Manufacturing Engineer, Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Staff Process Engineer

We are supporting a leading biopharmaceutical organization in Massachusetts seeking a Senior Staff Process Engineer with deep, hands‑on expertise in thin film or wiped film evaporation systems within GMP manufacturing environments.

This is a high‑visibility engagement supporting advanced oligonucleotide production at commercial scale.

This is not a pilot or lab role. We are looking for engineers who have owned evaporative concentration and solvent removal systems in real GMP production environments. This opportunity is ideal for senior process engineers who have led thin film evaporation operations at commercial scale and are looking to support a high‑impact manufacturing engagement.

Responsibilities
  • Serve as subject matter expert for thin film / wiped film evaporation systems
  • Support process design, scale‑up, and equipment optimization
  • Lead troubleshooting related to heat transfer, viscosity control, and solvent removal
  • Develop and review PFDs, P&IDs, URS documentation, and technical specifications
  • Support FAT/SAT, commissioning, and startup activities
  • Partner with Manufacturing, Quality, and Engineering teams to ensure compliant execution
Required Qualifications
  • 10–15+ years of process engineering experience in pharmaceutical, biotech, or CDMO environments
  • Direct hands‑on experience with thin film or wiped film evaporators
  • Experience in solvent‑heavy GMP production environments
  • Strong understanding of GMP manufacturing requirements
  • Experience supporting commissioning, startup, and operational troubleshooting
Preferred Experience
  • Oligonucleotide or RNA therapeutic manufacturing
  • Commercial API or complex drug substance production
  • Equipment lifecycle ownership from design through startup

Please do not contact if you are a third party vendor.

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