Process Engineer - Large Molecule

Source One Technical Solutions, LLC; Wilson (NC); On-site; USD 115,000 - 117,000; Full time

Job summary

Source One Technical Solutions, LLC is seeking a junior-level Process Engineer to support the design, start-up, and operational readiness of GMP LMDS manufacturing facilities for a global pharmaceutical client in Wilson, NC. The role involves engineering activities across equipment, utilities, automation, and facility systems, working with senior engineering and manufacturing teams.

The ideal candidate has a foundational GMP background, a degree in Chemical or Mechanical Engineering, and 1–3

Qualifications

• Bachelor’s degree in Chemical or Mechanical Engineering required.
• 1–3 years of process or plant engineering experience in GMP environments preferred.
• Exposure to biologics/pharma manufacturing is preferred.

Responsibilities

• Support engineering design, commissioning, start-up, and operations for biologics systems.
• Assist with process engineering for equipment, utilities, automation, and facility systems.
• Support tech transfer and manufacturing readiness activities.
• Participate in CAPEX projects and start-up initiatives.
• Coordinate with external engineering firms, construction teams, and vendors.
• Collaborate with Manufacturing, Quality, Engineering, and Technical Operations.
• Assist in troubleshooting process issues and implement solutions.
• Ensure GMP compliance and safety standards.
• Develop technical documentation and engineering reports.

Skills

GMP manufacturing experience

Process engineering fundamentals

Cross-functional collaboration

Education

Bachelor's degree in Chemical Engineering or Mechanical Engineering

Job description

Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical manufacturing client in Wilson, NC.

No Third-Party, No Corp to Corp, No Sponsorship Now, Future or Temporary Authorization

Junior Process Engineer – Large Molecule Drug Substance (LMDS)

Pay Rate: $55.57/hr (w2)

Location: Wilson, NC

Contract: 24 months

Travel: Domestic travel up to 10% (primarily annual project/site support)

Position Summary

We are seeking a junior-level Process Engineer to support the design, start-up, and operational readiness of GMP large molecule biologics manufacturing facilities. This role will support process engineering activities across manufacturing equipment, utilities, automation, and facility systems while working closely with senior engineering and manufacturing teams. The ideal candidate will have foundational GMP manufacturing knowledge, strong technical aptitude, and the ability to support engineering projects in a regulated biologics manufacturing environment.

Key Responsibilities

• Support engineering design, commissioning, start-up, and operational support activities for biologics manufacturing systems and equipment
• Assist with process engineering support for manufacturing equipment, utilities, automation, and facility systems
• Support technology transfer and manufacturing readiness activities to ensure alignment with operational and engineering standards
• Participate in CAPEX projects, process improvements, and start-up initiatives within GMP manufacturing environments
• Coordinate with external engineering firms, construction teams, and equipment vendors to support project execution and timelines
• Collaborate cross-functionally with Manufacturing, Quality, Engineering, and Technical Operations teams to support project objectives and operational needs
• Assist in troubleshooting manufacturing and process-related issues and support implementation of engineering solutions
• Ensure compliance with GMP regulations, safety standards, and company engineering procedures
• Support development of technical documentation, project deliverables, and engineering reports

Education

• Bachelor’s degree in Chemical Engineering or Mechanical Engineering required
• Advanced degree or PE certification preferred but not required

Experience and Skills

• Minimum 1–3 years of process or plant engineering experience within GMP manufacturing environments preferred
• Exposure to biologics, pharmaceutical, or regulated manufacturing operations preferred
• Basic understanding of process systems, utilities, automation, and facility operations
• Experience supporting manufacturing start-up, commissioning, or equipment qualification activities is a plus
• Strong analytical, problem-solving, and organizational skills
• Ability to work effectively within cross-functional teams and communicate with internal and external stakeholders
• Working knowledge of GMP regulations and manufacturing processes preferred

Top 3 Non-Negotiable Skills

• GMP or regulated manufacturing experience
• Process engineering fundamentals within manufacturing environments
• Exposure to equipment, utilities, or manufacturing systems support