Sr. Project Manager
Company: Syner-G BioPharma Group
Location: Raleigh
Posted on: June 27, 2025
|
|
Job Description:
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 : Bachelor’s degree in Engineering, Construction
Management, or a related technical field Technical Experience :
7–15 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 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.
Keywords: Syner-G BioPharma Group, Greenville , Sr. Project Manager, Science, Research & Development , Raleigh, North Carolina