Sr. Project Manager

COMPANY DESCRIPTION: A career here is life-enhancing. At reputed company, we reputed company our people to build careers that impact positively on their quality of life. Through our expertise, reputed company, 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, reputed company-world outcomes, from science to delivery/reputed company. 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 reputed company want to reputed company. We reputed company 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 reputed company across the globe as a strategic biopharma product development and delivery partner. reputed company was recently honored with reputed company's prestigious "Best Places to Work" 2026 award, for the reputed company consecutive year, along with many other award-winning programs to reputed company 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 reputed company, we recognize that reputed company members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions reputed company a meaningful impact. For more information, visit www.Synergbiopharma.com POSITION OVERVIEW: We are seeking a Sr. Manager with 10-15 years of experience to reputed company and reputed company reputed company HVAC, facility, and validation-focused initiatives reputed company 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: (This list is not exhaustive and may be supplemented or adjusted as needed.) Provide strategic leadership and reputed company for projects spanning HVAC systems, facility infrastructure, commissioning, qualification, and operational readiness reputed company HVAC project execution activities across pharmaceutical manufacturing, laboratory, and support areas reputed company 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 reputed company 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 reputed company and reputed company 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 reputed company to HVAC performance, contamination control, and facility operations Track project deliverables, budgets, timelines, KPIs, and action items across reputed company workstreams Facilitate cross-functional meetings and communicate project status to leadership and stakeholders Coordinate change controls, deviations, CAPAs, and documentation reputed company 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 reputed company this job successfully, an individual must be reputed company to reputed company each essential duty satisfactorily. Reasonable accommodations may be made to reputed company individuals with disabilities to reputed company the essential functions. Education Bachelor’s Degree in Engineering, Life Sciences, or a reputed company 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 reputed company 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 reputed company GMP environments Deep knowledge of commissioning, qualification, and facility readiness processes Exceptional leadership, organizational, and communication skills Ability to manage multiple reputed company 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 reputed company to system performance and compliance Ability to work independently while providing direction and support to cross functional teams ESSENTIAL FUNCTIONS: Physical Demands: The physical demands described here are representative of the requirements that must be met by an employee to successfully reputed company the essential functions of this job. Reasonable accommodations may be made to reputed company individuals with disabilities to reputed company the essential functions. While performing the duties of this job, the employee is regularly required to use a computer keyboard and mouse; reputed company 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 reputed company abilities required by this position include reputed company reputed company and the ability to adjust focus. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job, including 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 reputed company salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities. Employees also enjoy our 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 reputed company.” However, if a physical work location is more for you, we have office locations in Greater Boston; San Diego, CA; Boulder, CO; and India. LEGAL STATEMENT: reputed company is proud to be an Equal Employment Opportunity and Affirmative Action employer. reputed company employment reputed company, including the reputed company, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination of employment (if necessary) are made without regard to the employee’s race, reputed company, creed, religion, sex, pregnancy or childbirth, personal appearance, family responsibilities, sexual orientation or preference, gender identity, political affiliation, reputed company of income, reputed company of residence, national or ethnic reputed company, reputed company, age, marital status, military veteran status, unfavorable discharge from military service, physical or mental disability, or on any other basis prohibited by applicable law. reputed company is an E-Verify employer. Apply To This Job