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Syner-G

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. 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.

Senior Facilities Engineer

EngineerEngineerFull TimeRemoteSeniorTeam 201-500

Location

Worldwide

Posted

22 days ago

Salary

0

Seniority

Senior

Job Description

Senior Facilities Engineer

Syner-G

Role Description Syner-G is seeking a Senior Facilities Engineer with 5–10 years of experience supporting and leading commissioning, qualification, validation, and ongoing operation of GMP facility systems across laboratory, manufacturing, and utility environments. This role combines facilities engineering ownership (utilities, maintenance, infrastructure) with CQV lifecycle execution, ensuring that facility systems are designed, commissioned, qualified, maintained, and compliant with GMP and regulatory expectations. The Senior Engineer will act as a technical subject matter expert across facility systems, lead validation efforts, support lifecycle management, mentor junior staff, and collaborate cross-functionally to ensure safe, reliable, and inspection-ready operations. Work Location Travel to client sites may be required up to 100%, depending on project demands and client expectations. Key Responsibilities - Lead and execute commissioning, qualification, and validation (CQV) activities for facility systems, utilities, and GMP infrastructure such as HVAC, clean utilities, process gases, and electrical systems. - Develop and approve validation lifecycle documentation including user requirements specifications (URS), design qualification (DQ), installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). - Support risk assessments such as FMEA and system classification (GxP vs. non-GxP). - Ensure systems are designed and maintained in alignment with GMP, ISPE guidance, and regulatory requirements. - Lead commissioning readiness, system turnover, and release to operations. - Support periodic review, requalification, and change control activities. - Oversee operation, maintenance, and reliability of critical facility systems and utilities including HVAC, chilled water, steam, WFI, compressed air, process gases, electrical systems, and building management systems (BMS/EMS). - Lead, schedule, and manage corrective maintenance and preventative maintenance programs. - Conduct system monitoring and performance trending to ensure reliability and compliance. - Perform inspections and drive continuous improvement initiatives for facility systems. - Maintain and verify engineering documentation including P&IDs, electrical one-lines, and airflow diagrams. - Lead troubleshooting and root cause investigations for utilities, GMP equipment, and infrastructure. - Support deviation investigations and CAPA development. - Respond to alarms, system failures, and emergency events with technical leadership. - Ensure all systems remain in a validated and audit-ready state. - Maintain documentation in compliance with SOPs, GMP requirements, and data integrity standards. - Support internal and external audits and regulatory inspections. - Partner with Engineering, Manufacturing, Quality, Validation, and R&D to support operations and projects. - Provide engineering support for capital projects including design review, FAT/SAT, and commissioning activities. - Ensure smooth transition from project CQV phases into steady-state facilities operations. - Serve as a technical subject matter expert and mentor junior engineers and technicians. - Manage multiple projects and priorities with minimal oversight. Qualifications - Bachelor’s degree in Engineering (Mechanical, Chemical, Electrical preferred) or a related technical field. - 5–10 years of experience in CQV, validation engineering, facilities engineering, or a blended role. - Strong experience supporting GMP utilities, cleanroom environments, and facility systems. - Experience with commissioning and qualification of facility and utility systems. - CAPEX project experience is preferred. - Strong understanding of CQV lifecycle and validation principles. - Knowledge of GMP regulations (FDA, EMA) and data integrity requirements. - Experience with utilities and infrastructure systems in regulated environments. - Familiarity with ISPE guidance and ASTM E2500 is preferred. - Strong troubleshooting, root cause analysis, and problem-solving skills. - Ability to develop and interpret engineering and validation documentation. - Excellent communication, leadership, and collaboration skills. - Highly organized and capable of balancing project-based work with ongoing operations support. Benefits - Market competitive base salary and annual incentive plan. - Robust benefit offerings. - Ongoing recognition and career development opportunities. - Generous flexible paid time off program. - Company-paid holidays. - Flexible working hours and fully remote work options for most positions. - Office locations in Greater Boston; San Diego, CA; Boulder, CO; and India for those who prefer a physical work location.

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