Biopharma Process Engineer — cGMP On‑Site Ops

Arcadis; Lexington (MA); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Medical, Dental, and Vision

401(k)

Paid parental leave

Tuition reimbursement

Job summary

A leading engineering firm is seeking mid-level Process Engineers to provide on-site support for biomanufacturing systems in Massachusetts. The role requires a Bachelor's degree in relevant engineering fields and 3–7 years of experience. Responsibilities include executing maintenance tasks and supporting engineering teams. The firm values diverse backgrounds and offers comprehensive benefits including medical, 401(k), and paid time off.

Qualifications

• 3–7 years of relevant process engineering experience in a cGMP biopharmaceutical or pharmaceutical manufacturing environment.
• Familiarity with engineering specifications and P&IDs.
• Ability to interpret technical drawings.

Responsibilities

• Execute and document Preventive Maintenance work orders.
• Conduct functional equivalency evaluations for replacement parts.
• Support full-time engineers during deviation investigations.

Skills

Problem-solving

Root-cause analysis

Data trending

Collaboration

Education

Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering

Tools

Veeva

IBM Maximo

Siemens COMOS

OSIsoft PI

Microsoft Suite

Job description

A leading engineering firm is seeking mid-level Process Engineers to provide on-site support for biomanufacturing systems in Massachusetts. The role requires a Bachelor's degree in relevant engineering fields and 3–7 years of experience. Responsibilities include executing maintenance tasks and supporting engineering teams. The firm values diverse backgrounds and offers comprehensive benefits including medical, 401(k), and paid time off.