Process & Validation Engineer

Overview

Avantor is looking for a Process Engineer to be responsible for multiple phases of manufacturing processes and process improvement projects. The Process Engineer implements process improvements to meet quality standards, designs and conducts feasibility studies, and solves problems. They develop and execute validation of equipment and processes, create necessary documentation, and aid in communication to personnel while serving as a resource to site associates and coordinating work within the scope of assigned projects.

This is a full‑time position at our Devens, MA location.

• Support production operations by assisting with basic process analysis and identifying routine issues under supervision.
• Perform data collection and assist with simple data entry, data trending, and basic data review.
• Participate in introductory problem‑solving activities such as 5
  
  Whys or basic root‑cause discussions, with guidance.
• Assist in preparing and executing validation or qualification tasks for equipment and processes as directed by senior staff.
• Communicate with process owners and operators to gather feedback and help verify process performance.
• Support continuous improvement efforts by documenting observations, collecting metrics, and participating in improvement activities.
• Assist in drafting or updating SOPs, work instructions, and training materials under supervision.
• Provide basic troubleshooting support for equipment or hardware issues, escalating more complex problems to senior team members.
• Perform additional duties as assigned.

• Education: Bachelor’s degree in Industrial Engineering, Chemical Engineering, Mechanical Engineering, Biology, Chemistry, or a related technical field.
• Experience (0–1
  
  Year): Exposure to regulated environments (FDA or ISO
  9001) through coursework, internships, or entry‑level work; familiarity with GMP manufacturing concepts; basic understanding of project coordination or participation in academic projects; proficiency with MS Office Suite (Excel, Word, PowerPoint).
• 
  
  Preferred Experience (1–2
  
  Years): Experience in biopharma manufacturing or cleanroom environments; familiarity with software tools such as Access, Visio, or Minitab; exposure to Lean Manufacturing or Six Sigma concepts; participation in continuous improvement or process‑related academic projects.

ENVIRONMENTAL WORKING CONDITIONS & PHYSICAL EFFORT:
The noise level in the work environment ranges with typical noise level equivalent to office functions but exposed to warehouse traffic and forklift noises. Work is primarily conducted in office spaces, clean rooms, or warehouses. Exposure to non‑climate‑controlled environments is expected. Employees receive workplace safety training and are expected to maintain a safe environment, obey safety rules, and exercise caution in all work activities.

The expected pre‑tax pay for this position is $52,000.00 – $83,950.00. Actual pay may differ depending on relevant factors such as prior experience and geographic location.

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at r and let us know the nature of your request and your contact information.

Requests for accommodation will be considered on a case‑by‑case basis.