Project Manager

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:
We are seeking a Project Manager with a strong background in capital project execution within biologics manufacturing environments. This role will focus on the technical planning, coordination, and execution of projects involving drug substance, drug product, and supporting infrastructure (e.g., utilities, warehouse). The ideal candidate will bring a blend of engineering expertise and project leadership, ensuring projects are delivered on time, within budget, and in compliance with GMP and regulatory standards.

WORK LOCATION:
This role may require travel to client sites up to 100%, depending on project phase and client needs.

KEY RESPONSIBILITIES:

• Lead and execute capital projects from concept through commissioning and qualification
• Develop and manage project scopes, schedules, and budgets with a focus on engineering deliverables and construction readiness
• Coordinate with cross-functional teams including process engineering, automation, validation, and quality to ensure technical alignment
• Manage external design and engineering firms to develop compliant and constructible designs
• Oversee construction activities, ensuring adherence to design specifications, safety standards, and GMP requirements
• Prepare and evaluate RFPs for construction and commissioning vendors
• Support equipment selection, utility integration, and facility layout planning
• Drive risk assessments and implement mitigation strategies throughout the project lifecycle
• Maintain project documentation including technical drawings, specifications, and change controls
• Ensure seamless handover to operations and facilities teams post-project completion
• Promote continuous improvement in project execution methodologies and engineering standards

QUALIFICATIONS AND REQUIREMENTS:

Education

• Bachelor’s degree in Engineering (Mechanical, Chemical, Electrical, or related field) or Construction Management

Experience

• 3–7 years of experience in project engineering or project management within biologics or life sciences manufacturing
• Hands-on experience with facility design, utility systems, and process equipment integration
• Familiarity with GMP environments and regulatory compliance
• Proven ability to manage technical teams and external contractors
• Experience with capital budgeting and cost control

Skills & Abilities

• Strong technical problem-solving and analytical skills
• Excellent communication and stakeholder management abilities
• Proficiency in project management tools (e.g., MS Project, Primavera, or similar)
• Ability to manage multiple projects in a fast-paced, regulated environment

ESSENTIAL FUNCTIONS & WORK ENVIRONMENT:

• Regular use of computers and office equipment
• Occasional lifting of materials up to 25 pounds
• Work may occur in both office and active construction or manufacturing environments

TOTAL REWARDS & COMPENSATION:
We offer a comprehensive total rewards package including competitive salary, annual incentives, flexible work arrangements, generous PTO, and professional development opportunities.

The expected salary range for this role is $106,000 to $130,000, based on experience and location.

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.