Process Engineer III

About the Role

We're seeking an experienced Process Engineer III to support the transfer, validation, and optimization of chemical manufacturing processes in a fast-paced life sciences manufacturing environment. This is a hands-on engineering role focused on process scale-up, equipment validation, continuous improvement, and cross-functional collaboration.

This is an excellent opportunity for an engineer with a strong background in chemical process development, GMP manufacturing, and process validation who enjoys solving complex manufacturing challenges.

Responsibilities

• Lead technology transfer activities for chemical manufacturing processes.
• Plan and execute equipment and process validations, including IQ/OQ/PQ protocols.
• Develop process flow diagrams, mass and energy balances, and manufacturing documentation.
• Perform and facilitate process risk assessments, including FMEA and HAZOP analyses.
• Investigate process deviations, identify root causes, and implement corrective and preventive actions (CAPAs).
• Drive process optimization and scale-up initiatives using data-driven decision-making.
• Develop work instructions and manufacturing procedures to support production.
• Partner with manufacturing, quality, engineering, and operations teams to improve efficiency and product quality.
• Champion a strong culture of safety, quality, and continuous improvement.

Qualifications

• Bachelor's degree (or higher) in Chemical Engineering or a related engineering discipline.
• 7+ years of process engineering experience within chemical manufacturing or a closely related regulated industry.
• Hands-on experience with:
  • Technology transfer of chemical manufacturing processes
  • Equipment and process validation (IQ/OQ/PQ)
  • cGMP manufacturing environments
  • Risk assessments (FMEA, HAZOP)
  • Deviation investigations and change control
  • Process optimization and scale-up
• Strong understanding of process engineering principles and manufacturing documentation.
• Experience working with cross-functional teams in regulated manufacturing environments.

Preferred Experience

• Life sciences, biotechnology, pharmaceutical, specialty chemical, or advanced manufacturing industries.
• Process development supporting commercial manufacturing.
• Continuous improvement initiatives that improve throughput, quality, or operational efficiency.

Skills

• Knowledge of Lean Manufacturing, Six Sigma, or Statistical Process Control (SPC) is a plus.

Pay & Schedule

• Duration: 6-month contract
• Pay rate: $60–$80/hour (higher rates considered for exceptional candidates)
• Location: Sudbury, MA
• Schedule: Monday – Friday, 100% onsite