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.While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required.No Third-Party, No Corp to Corp, No Sponsorship Now, Future or Temporary AuthorizationJunior Process Engineer – Large Molecule Drug Substance (LMDS)Pay Rate: $55.57/hr (w2)Location: Wilson, NCContract: 24 monthsTravel: Domestic travel up to 10% (primarily annual project/site support)Position SummaryWe 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 ResponsibilitiesSupport engineering design, commissioning, start-up, and operational support activities for biologics manufacturing systems and equipmentAssist with process engineering support for manufacturing equipment, utilities, automation, and facility systemsSupport technology transfer and manufacturing readiness activities to ensure alignment with operational and engineering standardsParticipate in CAPEX projects, process improvements, and start-up initiatives within GMP manufacturing environmentsCoordinate with external engineering firms, construction teams, and equipment vendors to support project execution and timelinesCollaborate cross-functionally with Manufacturing, Quality, Engineering, and Technical Operations teams to support project objectives and operational needsAssist in troubleshooting manufacturing and process-related issues and support implementation of engineering solutionsEnsure compliance with GMP regulations, safety standards, and company engineering proceduresSupport development of technical documentation, project deliverables, and engineering reportsEducationBachelor's degree in Chemical Engineering or Mechanical Engineering requiredAdvanced degree or PE certification preferred but not requiredExperience and SkillsMinimum 1–3 years of process or xhyhwjd plant engineering experience within GMP manufacturing environments preferredExposure to biologics, pharmaceutical, or regulated manufacturing operations preferredBasic understanding of process systems, utilities, automation, and facility operationsExperience supporting manufacturing start-up, commissioning, or equipment qualification activities is a plusStrong analytical, problem-solving, and organizational skillsAbility to work effectively within cross-functional teams and communicate with internal and external stakeholdersWorking knowledge of GMP regulations and manufacturing processes preferredTop 3 Non-Negotiable SkillsGMP or regulated manufacturing experienceProcess engineering fundamentals within manufacturing environmentsExposure to equipment, utilities, or manufacturing systems support
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