Sr. Project Engineer

COMPANY DESCRIPTION:   A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery/success. To learn more about who we are and what drives us, watch our company video here .  Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner. Syner-G was recently honored with BioSpace's prestigious "Best Places to Work" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation.  At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact.  For more information, visit www.Synergbiopharma.com POSITION OVERVIEW: We are seeking a Sr. Project Engineer with 2–5 years of experience supporting engineering, commissioning, validation, and operational readiness activities within GMP-regulated life sciences environments. The ideal candidate will have hands-on experience supporting capital projects, facility and utility systems, engineering documentation, and cross-functional project execution. Prior validation experience supporting capital projects is preferred. This role is suited for an engineer who has developed a solid technical foundation and is ready to take on increased responsibility in coordinating and executing engineering, validation, and commissioning activities throughout the project lifecycle. WORK LOCATION: Travel to client sites may be required up to 100%, depending on project needs and client expectations. KEY RESPONSIBILITIES: (This list is not exhaustive and may be supplemented or adjusted as needed.) Support the execution of capital projects from design through commissioning, qualification, validation, and startup activities. Perform startup and commissioning of building and utility systems such as HVAC, chilled water, water systems, electrical systems, fire protection, pH neutralization, and waste systems. Support validation and qualification activities, including protocol development, execution, discrepancy resolution, and final reporting. Generate and manage engineering and validation lifecycle documentation, including impact assessments, URS/FRS documents, FAT/SAT documentation, commissioning protocols, qualification protocols, ETOPs, and P&IDs. Conduct drawing walkdowns and verify field installation of equipment, facilities, and utility systems. Develop and execute commissioning and qualification protocols and reports. Support troubleshooting, issue resolution, and risk assessments during commissioning, qualification, and startup activities. Utilize systems such as BMS, PCS, and CMMS; experience with KNEAT is a plus. Coordinate with cross-functional teams including engineering, facilities, validation, operations, quality, and project management to support project deliverables. Assist in planning and scheduling project tasks, tracking progress, and ensuring timely completion of milestones. Communicate effectively with stakeholders to provide updates, escalate issues, and maintain alignment across project teams. Ensure all work complies with GMP, safety, quality, and regulatory requirements. QUALIFICATIONS AND REQUIREMENTS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education Bachelor's Degree in Engineering or a related technical field. Technical Experience 2–5 years of experience in engineering, commissioning, validation, facilities, or operations within a GMP-regulated pharmaceutical, biotechnology, or industrial environment. Experience supporting capital projects within GMP-regulated manufacturing or facility environments. Prior validation experience supporting capital projects is preferred. Hands-on experience with startup, commissioning, qualification, or validation of facility, utility, equipment, or process systems. Experience generating and managing engineering and validation documentation. Experience with drawing walkdowns, field verification, and construction turnover activities. Familiarity with cGMP documentation practices and validation lifecycle methodologies. Familiarity with BMS, PCS, CMMS, or similar technical systems. Experience with KNEAT or digital validation documentation platforms is a plus. Knowledge, Skills, and Abilities Strong understanding of facility, utility, equipment, and process systems within regulated manufacturing environments. Working knowledge of commissioning, qualification, validation, and capital project execution methodologies. Excellent documentation, organizational, and technical writing skills. Ability to manage multiple tasks, priorities, and deadlines in