Job description
COMPANY DESCRIPTION:
Syner-G BioPharma Group and Sequoia Biotech Consulting recently merged in September 2024, uniting two industry leaders to create a new force in life sciences consulting. By combining our expertise in product development, regulatory strategy, quality and compliance and commercial manufacturing, we are positioned to deliver fully integrated solutions across the development continuum.
We are helping to enhance human health. This merger strengthens our ability to accelerate groundbreaking therapies and help clients navigate the complex life sciences landscape with greater agility and confidence. Together, we form a leading life sciences consultancy dedicated to empowering organizations to overcome complex challenges and accelerate the speed to market, scale and quality of life-saving innovations.
We work across a diverse range of clients and projects, supporting many organizations through the most critical phases of the drug discovery, approval, product development, technology transfer and commercial manufacturing process. We also equip our partners with the tools, knowledge and expertise to streamline operations, enhance quality and ensure compliance.
Syner-G BioPharma Group was recently honored with BioSpace’s prestigious “Best Places to Work” 2025 award, for the second 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 and Sequoia, 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.Sequoiabiotech.com/ or www.Synergbiopharma.com
POSITION OVERVIEW :
Seeking an experienced Sr. Project Manager to act as an owner’s representative on large, complex construction projects, preferably in lab/office or cGMP manufacturing environments. The ideal candidate will have 7-12 years of experience, strong leadership and communication skills, and a deep understanding of safe construction practices, with a proven track record in commissioning, project management, and compliance with cGMP standards.
WORK LOCATION:
Travel to client sites may be required up to 100%, based on project demands and client expectations.
KEY RESPONSIBILITIES :
(This list is not exhaustive and may be supplemented and changed as necessary.)
Act as owner’s representative on large, complex construction projects, preferably in lab/office or cGMP manufacturing environments.
Work on multi-employer sites (more than one contractor on a single construction site).
Take projects from design through construction and into commissioning.
Write commissioning strategy/plan and protocols for large projects.
Review technical submissions from all team members: Architectural and Engineering firms, System Integrators, equipment manufacturers, and the owner’s own engineering groups (local and global) to ensure all necessary components are in place for system installation and commissioning.
Answer common construction communications like RFIs, Submittals, etc.
Work as part of a larger construction team to schedule the work of the commissioning team and the moving company to meet both cost and schedule targets.
Supervise a large sub-contractor team that will start-up and commission all equipment in a large capital project.
Coordinate the purchase, receipt, and movement of equipment into a facility that may not be complete from a construction perspective.
Schedule the decommissioning, packing, movement, and ultimate unpacking of large amounts of equipment from one facility to another.
Review all construction site safety documents like work permits, task plans, job hazard analyses, and ensure the System Integrator executes all work in compliance with procedures and safety standards.
Walk construction sites, take part in daily planning meetings, and document observations.
Use at least one project/construction management software package like ProCore, E-Builder, Prolog, etc.
Design, start-up, commission, and hand over common lab and office building systems like Building Automation Systems (BAS), HVAC systems, emergency power and UPS systems, lab gases, RODI water, boilers, steam generators, etc. (experience in a GMP environment is a plus but not required).
Write operational and maintenance SOPs for all building systems like calibration procedures, preventative maintenance, lockout/tagout, access control, etc.
Successfully close out large projects, ensuring all necessary documentation is in place, accurate, and all financial obligations are met.
Use a CMMS like Maximo, Blue Mountain, etc., and set up large numbers of assets inside the CMMS.
QUALIFICATIONS AND REQUIREMENTS :
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the education, experience, skills, knowledge, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.
Education :
- An engineering degree (mechanical, electrical, construction).
Technical Experience :
4-9 years of experience on large, complex engineering projects, preferably in a mix of validation contractors and operating companies as a project engineer/manager.
3-5 years of relevant experience within the biotech industry with proven knowledge of current Good Manufacturing Procedures (cGMP) compliance.
Experience acting as owner’s representative on large, complex construction projects.
Experience working on multi-employer sites.
Experience taking projects from design through construction and into commissioning.
Experience writing commissioning strategy/plans and protocols for large projects.
Experience supervising a large sub-contractor team for start-up and commissioning of equipment.
Experience coordinating the purchase, receipt, and movement of equipment.
Experience scheduling the decommissioning, packing, movement, and unpacking of equipment.
Experience reviewing construction site safety documents and ensuring compliance.
Experience using project/construction management software like ProCore, E-Builder, Prolog, etc.
Experience designing, starting up, commissioning, and handing over lab and office building systems.
Experience writing operational and maintenance SOPs for building systems.
Experience closing out large projects and ensuring documentation and financial obligations are met.
Experience using a CMMS like Maximo, Blue Mountain, etc.
Knowledge, Skills, and Abilities :
An OSHA construction certification.
A deep understanding of safe construction practices and standards.
Strong leadership, collaboration, communication, prioritization, and problem-solving skills.
Highly motivated, independent, detail-oriented team player with good organization, initiative, and a collaborative attitude.
ESSENTIAL FUNCTIONS :
Physical Demands :
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.
- While performing the duties of this job, the employee is regularly 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 by this position include close vision 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 base 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 anywhere”. However, if a physical work location is more for you, we have office locations in Greater Boston; San Diego, CA; Boulder, CO; and India.
COMPENSATION :
The expected salary range for this position is $107,000 to $153,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.
Applicants must have current work authorization when accepting a position at Syner-G. Currently, Syner-G is unable to sponsor or take over sponsorship of an employment Visa at this time.
LEGAL STATEMENT:
Syner-G BioPharma Group and Sequoia Biotech Consulting are proud to be an Equal Employment Opportunity and Affirmative Action employers. All employment decisions, including the recruiting, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination of employment (if necessary) 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 BioPharma is an E-Verify employer.
