Sr. Project Engineer

Syner-G • Marlborough, MA

1d • Onsite

About The Position

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. 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.

Requirements

• Bachelor's Degree in Engineering or a related technical field.
• 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.
• 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.
• 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 a fast-paced project environment.
• Strong communication and interpersonal skills.
• Detail-oriented with strong analytical and problem-solving abilities.
• Ability to work independently and collaboratively across multidisciplinary teams.

Nice To Haves

• Prior validation experience supporting capital projects is preferred.
• Experience with KNEAT or digital validation documentation platforms is a plus.

Responsibilities

• 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.

Benefits

• Market competitive base salary
• Robust benefit offerings
• Ongoing recognition and career development opportunities
• Generous paid time away program
• Company-paid holidays

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level