Sr. Project Manager

COMPANY DESCRIPTION:

Syner-G BioPharma Group is a science-led, strategic partner for life science companies. We provide integrated regulatory and biopharmaceutical development services spanning early development to post-market, along with operational strategy and support. With a global team of 400 employees across North America and India, our goal is to help our partners navigate the complexities of product development and accelerate their journey to market.

We are a leading life sciences consultancy committed to advancing human health by helping organizations bring life-saving innovations to market faster, at scale, and with the highest quality.

Our team partners with a diverse range of clients across the life sciences industry, supporting critical phases of the drug development lifecycle, from discovery and regulatory approval to technology transfer and the support in capital projects. We provide strategic guidance and hands-on expertise to streamline operations, enhance quality systems, and ensure regulatory compliance, empowering our clients to navigate complexity and deliver impactful therapies to patients worldwide.

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, 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.Synergbiopharma.com

POSITION OVERVIEW:

We are seeking a Sr. Project Manager with experience in capital project execution and delivery within biologics manufacturing, including drug substance, drug product, and warehouse/utilities infrastructure. The ideal candidate will be responsible for capital project funding approvals, managing design firms, budgeting/scheduling, and leading projects through execution. This role requires strong cross-functional collaboration with design, engineering, construction, and facilities teams, as well as the ability to work effectively with internal stakeholders in a regulated environment.

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.)

• Lead large capital projects from pre-construction through execution, ensuring alignment with project goals and timelines
• Develop and manage capital budgets for biologics manufacturing and infrastructure projects, ensuring cost-effective solutions and adherence to financial constraints
• Engage and manage design teams to develop compliant project plans and specifications
• Oversee execution of projects including construction, commissioning, and qualification, ensuring minimal disruption to operations
• Process Construction Manager (CM) and commissioning RFPs, ensuring comprehensive and competitive proposals
• Provide technical expertise in biologics facility design, utilities, and GMP compliance
• Collaborate with engineering, quality, validation, and facilities teams to ensure seamless project integration
• Work closely with stakeholders to understand project requirements and ensure alignment with business needs
• Develop and maintain project schedules, ensuring timely completion of milestones and deliverables
• Identify project risks and implement mitigation strategies to ensure successful outcomes
• Manage project documentation, including budgets, schedules, and technical specifications
• Ensure compliance with all relevant regulations, standards, and internal quality systems
• Drive continuous improvement initiatives to enhance project management processes and outcomes

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 :

• Bachelors degree in Engineering, Construction Management, or a related technical field

Technical Experience :

• 715 years of experience in capital project management within biologics or life sciences manufacturing
• Proven experience delivering projects in drug substance, drug product, and warehouse/utilities environments
• Strong knowledge of GMP requirements, facility design, and process integration
• Experience with capital budgeting and financial management
• Demonstrated success in managing design teams and external contractors
• Experience with shutdown/startup planning in operational manufacturing settings
• Strong understanding of project management principles and methodologies
• Demonstrated ability to manage multiple complex projects simultaneously

Knowledge, Skills, and Abilities :

• Excellent communication skills with the ability to work effectively across departments and influence stakeholders
• Strong leadership and team management abilities
• Detail-oriented with strong analytical and problem-solving capabilities
• Ability to work in a fast-paced, dynamic environment
• Proficiency in project management software and tools

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.

Currently, Syner-G is unable to sponsor or take over sponsorship of an employment Visa at this time.

LEGAL STATEMENT:

Syner-G BioPharma Group is 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 employees 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.