Process Engineer

Process EngineerAt Salas O'Brien we tell our clients that we're engineered for impact. This passion for making a difference applies just as much to our team as it does to our projects. That's why we are committed to living our values every day: inspiring, achieving, and connecting as shared owners of our success with a focus on a sustainable future. Building for the long-term means that all our team members can expect to work on amazing projects with a people-first approach to problem solving. It also means that each member of our team has truly limitless potential to build a unique, meaningful, and high-impact career—and they'll receive great total rewards along the way. Founded in 1975, Salas O'Brien is an employee-owned engineering and professional services firm focused on achieving impact for our clients, our team, and the world. We know that tomorrow's requirements are today's opportunities, and we are here to design lasting solutions for pressing challenges. We work across a variety of industries providing integrated engineering and consulting services.The Process Engineer supports capital project execution, engineering design, and ongoing improvements to systems and equipment within pharmaceutical and life sciences facilities operating under cGMP requirements. This role provides technical expertise across the full project and system lifecycle, from scope development and documentation through implementation, commissioning, qualification, and ongoing optimization. The engineer works on both greenfield builds and capital projects within operating facilities, in collaboration with engineering design, construction management, and CQV/start-up teams. Candidates without direct pharmaceutical experience will need to demonstrate clearly transferable experience in regulated manufacturing environments, such as critical utility systems, cleanrooms, or process equipment.ResponsibilitiesProject Support: Execute capital projects on greenfield builds and within operating facilities, from scope development through implementation, commissioning, and qualification.Collaboration: Work independently while asking questions early and drawing on the best internal, client, and industry resources to meet requirements accurately and efficiently.Documentation: Develop and maintain project documentation, including specifications, test plans, and progress reports.Communication: Keep clients, contractors, and project teams informed, in person and in writing, on scope, deliverables, and compliance requirements, at technical through executive levels.Innovation: Foster an environment where new ideas are discussed and developed collaboratively and help others work through resistance to change.Qualifications and ExperienceEducation: Bachelor's degree in engineering (Chemical, Mechanical, or equivalent preferred)Experience: >3 years working in pharmaceutical industry or relevant regulated industry.Technical Skills: Direct hands-on experience in cGMP regulated environments in clean utilities, process equipment, maintenance/reliability or manufacturing systems, and an understanding of how engineering activities integrate with controlled documentation, validation, and change control processes. Experience developing and interpreting engineering deliverables, including PFDs, P&IDs, equipment specifications, system design documentation, and CQV documentation. Experience supporting capital projects within operating facilities, including system upgrades, expansions, or process improvement.Adaptability: Flexibility and willingness to work on various projects and tasks, embracing new challenges with enthusiasm.Initiative: Demonstrated ability to work independently and take initiative to drive projects forward.Nice to Have: FE Certification Working knowledge using engineering tools and software platforms.Location: This is not a remote role. This position will be required to report to a client site in Raleigh, NC. Travel: Flexibility and willingness for travel based on project needs.Compensation & Benefits: Actual compensation will be determined based on a number of factors including skills, experience, qualifications, and location. This role is also eligible for performance-based bonuses, and a comprehensive U.S. based benefits package, including: Medical, dental, and vision insurance 401(k) with company match Paid time off and company holidays Wellness programs and employee assistance resources Professional development support For more information, visit our full benefits overview here.Equal Opportunity Employment Statement Salas O'Brien provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state/provincial, or local laws. Salas O'Brien will accommodate the disability-related needs of applicants as required by law.