Sr. Project Manager

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 POSITION OVERVIEW We are seeking a Sr. Manager with 10‑15 years of experience to lead and oversee complex HVAC, facility, and validation‑focused initiatives within GMP regulated life sciences environments. The ideal candidate will have extensive experience managing cross‑functional teams, driving HVAC and cleanroom projects, and ensuring alignment with organizational goals, regulatory expectations, and client requirements. This role requires strong leadership, deep understanding of HVAC systems, cleanroom environments, and CQV processes, and the ability to manage multiple high‑visibility workstreams from planning through execution and closeout. WORK LOCATION Travel to client sites may be required up to 100%, depending on project needs and client expectations. KEY RESPONSIBILITIES Provide strategic leadership and oversight for projects spanning HVAC systems, facility infrastructure, commissioning, qualification, and operational readiness. Lead HVAC project execution activities across pharmaceutical manufacturing, laboratory, and support areas. Develop and manage project plans, schedules, budgets, resource strategies, and risk mitigation activities across multiple workstreams. Coordinate HVAC scope with construction, CQV, automation, facilities, and manufacturing teams. Oversee cleanroom implementation including airflow design, pressurization cascades, and environmental control strategies to meet GMP requirements. Manage contractors, vendors, schedules, field execution, and punch list activities through project completion. Drive HVAC startup, commissioning, qualification (IQ/OQ/PQ), and validation activities in alignment with CQV strategies. Support cleanroom and GMP facility readiness activities, including environmental monitoring alignment and operational setup. Perform and lead field walkdowns, system inspections, and issue resolution for HVAC and facility systems. Ensure delivery of key milestones, commissioning deliverables, validation packages, and turnover documentation. Guide development and execution of commissioning plans, qualification protocols, and turnover packages. Partner with CQV teams to ensure design and user requirements translate effectively into validation documentation and execution. Ensure alignment with engineering standards, safety requirements, and GMP expectations. Identify risks and drive mitigation strategies related to HVAC performance, contamination control, and facility operations. Track project deliverables, budgets, timelines, KPIs, and action items across all workstreams. Facilitate cross‑functional meetings and communicate project status to leadership and stakeholders. Coordinate change controls, deviations, CAPAs, and documentation within quality systems (eQMS). Support operational readiness and transition from construction and CQV into facility operations. Utilize systems such as CMMS, eQMS, LMS, and digital validation platforms; experience with KNEAT is a plus. Mentor and support project managers, engineers, and coordinators to ensure high quality execution and professional development. 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, Life Sciences, or a related technical field. A Master’s degree or PMP certification is a plus. Technical Experience 10‑15 years of experience in GMP regulated environments (biotech, pharmaceutical, cell/gene therapy, or medical device). Strong experience with HVAC systems, cleanroom environments, and facility utilities (e.g., chilled water, steam, controls). Experience leading HVAC‑focused projects and managing multiple concurrent initiatives. Experience with CQV lifecycle activities including commissioning and qualification of HVAC systems. Experience with cleanroom standards, environmental monitoring, and contamination control principles. Experience conducting or overseeing field walkdowns, readiness checks, and operational verification. Familiarity with BMS/EMS systems and HVAC control strategies. Experience with GMP documentation, change control, deviations, and validation packages. Familiarity with CMMS, eQMS, LMS, or similar regulated systems. Experience with KNEAT or digital validation platforms is a plus. Knowledge, Skills, and Abilities Strong understanding of HVAC systems, airflow dynamics, and cleanroom design within GMP environments. Deep knowledge of commissioning, qualification, and facility readiness processes. Exceptional leadership, organizational, and communication skills. Ability to manage multiple complex workstreams and competing priorities in a fast paced environment. Strong interpersonal skills with the ability to influence and collaborate across engineering, CQV, and operations teams. Detail oriented with strong analytical and problem solving abilities, especially related to system performance and compliance. Ability to work independently while providing direction and support to cross functional teams. ESSENTIAL FUNCTIONS The physical demands described here are representative of the requirements that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is required to use a computer keyboard and mouse; reach with hands and arms; talk and listen. The employee is frequently required to walk and sit, as well as to lift and carry objects such as books and files weighing up to 25 pounds. The employee is occasionally required to stand, stoop, or kneel. Specific vision abilities required include close vision and the ability to adjust focus. Work environment characteristics include moderate noise level, an indoor temperate environment, and light levels that are bright and conducive to minimal eye strain, typical for an office environment. TOTAL REWARDS PROGRAM We define total rewards as compensation, benefits, remote work/flexibility, development, recognition, and our culture with programs that support each of our reward pillars. This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities. Employees also enjoy a generous flexible paid time off program, company‑paid holidays, flexible working hours, and fully remote work options for most positions and the ability to work almost anywhere. Office locations are in Greater Boston, San Diego, CA, Boulder, CO, and India. LEGAL STATEMENT Syner-G is proud to be an Equal Employment Opportunity and affirmative action employer. All employment decisions, including the recruiting, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination of employment are made without regard to the employee’s race, color, creed, religion, sex, pregnancy or childbirth, personal appearance, family responsibilities, sexual orientation or preference, gender identity, political affiliation, source of income, place of residence, national or ethnic origin, ancestry, age, marital status, military veteran status, unfavorable discharge from military service, physical or mental disability, or on any other basis prohibited by applicable law. Syner-G is an E‑Verify employer. #J-18808-Ljbffr