Pharma Process Engineer — cGMP & Capital Projects

Salas O’Brien, Inc.; Raleigh (NC); On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) with company match

Paid time off and holidays

Wellness programs and employee support

Professional development support

Job summary

Salas O’Brien, Inc. seeks a Process Engineer to support capital project execution and ongoing improvements in pharmaceutical and life sciences facilities operating under cGMP.

You will provide technical expertise across scope development, implementation, commissioning, qualification, and optimization, in greenfield and capital projects. The role requires hands-on cGMP experience, ability to collaborate with design/construction/CQV teams, and a focus on delivering compliant documentation and

Qualifications

• Bachelor’s degree in engineering (Chemical, Mechanical) or equivalent.
• >3 years in pharmaceutical or regulated industry.
• Hands-on experience in cGMP environments with clean utilities and process equipment.
• Experience developing/interpreting engineering deliverables: PFDs, P&IDs, equipment specs, system design and CQV docs.
• Experience supporting capital projects within operating facilities.

Responsibilities

• Execute capital projects on greenfield builds or within operating facilities from scope to qualification.
• Collaborate with design, construction, and CQV/start-up teams to move projects forward.
• Develop and maintain project documentation and progress reports; ensure controlled documentation.

Skills

cGMP experience

Process equipment

Capital projects

Documentation

Education

Bachelor’s degree in engineering

Job description

Salas O’Brien, Inc. seeks a Process Engineer to support capital project execution and ongoing improvements in pharmaceutical and life sciences facilities operating under cGMP.

You will provide technical expertise across scope development, implementation, commissioning, qualification, and optimization, in greenfield and capital projects. The role requires hands-on cGMP experience, ability to collaborate with design/construction/CQV teams, and a focus on delivering compliant documentation and