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Syner-G BioPharma Group
Engineering & Architecture 1d ago

Sr. Program Manager

Syner-G BioPharma Group
United StatesUnited States
Full-time
$140,000 to $179,000 yearly
Senior-Level

Job Description

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POSITION OVERVIEW:

Syner-G is seeking a Sr. Program Manager to provide strategic leadership and oversight for complex, multi-year engineering programs spanning multiple projects, technical workstreams, and stakeholder groups. This role is responsible for establishing program governance, driving cross-functional alignment, managing risk at the program level, and ensuring that engineering initiatives are delivered with excellence in quality, compliance, and performance. The Sr. Program Manager serves as a trusted advisor to clients and internal leadership, offering deep technical insight, long-term planning capability, and the ability to navigate highly complex organizational and technical environments.

KEY RESPONSIBILITIES:

(This list is not exhaustive and may be supplemented or adjusted as necessary.)

  • Provide executive-level leadership across large, complex engineering programs, ensuring alignment with client strategy, technical requirements, and organizational goals.
  • Develop and manage program governance structures, communication frameworks, reporting mechanisms, and decision-making processes.
  • Oversee program schedules, milestones, interdependencies, and resource allocation across multiple concurrent engineering projects.
  • Identify program-level risks, constraints, and opportunities, and develop mitigation strategies to maintain program performance and continuity.
  • Lead cross-functional coordination among engineering, operations, quality, safety, facilities, and other technical teams to ensure cohesive program execution.
  • Review engineering documentation, design packages, technical deliverables, and program requirements, providing guidance and direction as needed.
  • Facilitate communication between internal teams, external partners, contractors, and client leadership to ensure clarity, alignment, and timely decision-making.
  • Lead program steering committees, technical working groups, and executive-level program reviews.
  • Ensure program activities comply with applicable standards, regulatory requirements, and internal procedures.
  • Develop and manage program budgets, forecasts, and financial tracking, ensuring alignment with client expectations and long-term planning.
  • Oversee program-level change management processes, ensuring impacts are evaluated, documented, and communicated.
  • Drive continuous improvement initiatives, program optimization strategies, and long-term engineering planning.
  • Support commissioning, validation, and operational readiness activities at a program level when applicable.
  • Prepare program dashboards, executive summaries, and performance reports to communicate progress, risks, and strategic recommendations.
  • Serve as a senior advisor to clients, offering guidance on engineering strategy, program structure, organizational readiness, and best practices.

QUALIFICATIONS AND REQUIREMENTS:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements below represent the education, experience, skills, knowledge, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education:

  • Bachelor’s degree in engineering (mechanical, electrical, chemical, industrial, or related discipline) or a related technical field preferred.
  • Advanced certifications such as PMP or PgMP are a plus.

Technical Experience:

  • 18+ years of experience in engineering, program management, or senior technical leadership roles.
  • Extensive experience managing large, complex engineering programs involving multiple projects, stakeholders, and technical disciplines.
  • Experience working in regulated or technically intensive environments such as biotech, pharmaceutical, chemical, industrial, or advanced manufacturing.
  • Deep understanding of engineering processes, design coordination, technical documentation, and cross-functional program dependencies.
  • Experience leading program governance, risk management, resource planning, and stakeholder communication at a senior level.
  • Experience supporting or overseeing commissioning, validation, or operational readiness activities is preferred.
  • Experience collaborating with engineering, operations, quality, and safety teams to ensure cohesive program execution.

Knowledge, Skills, and Abilities:

  • Exceptional leadership and communication skills with the ability to influence and collaborate across diverse teams and organizational levels.
  • Proficiency with program and project management tools and methodologies.
  • Highly analytical, detail-oriented, and capable of solving complex technical and organizational challenges.
  • Ability to manage competing priorities and drive program execution in fast-paced, dynamic environments.
  • Ability to build and maintain strong relationships with clients, stakeholders, and cross-functional partners.

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.

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Syner-G BioPharma Group

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Syner-G BioPharma Group (operating under synergbiopharma.com) is a leading global provider of integrated scientific, technical, regulatory, and compliance consulting services for the pharmaceutical, biotechnology, and medical device industries. Founded in 2007 by seasoned pharmaceutical scientist Dr. Prabu Nambiar, the company operates as a premier strategic development and delivery partner, guiding innovators through the complex multi-phase drug development lifecycle from pre-clinical Investigational New Drug (IND) milestones to post-approval commercialization. Syner-G's core architecture revolves around its proprietary CMC 360™ framework, an end-to-end technical offering covering Chemistry, Manufacturing, and Controls (CMC) technical operations, regulatory affairs strategy, medical writing, and rigorous cGxP quality compliance. The company operates a functional outsourcing and strategic advisory model, partnering closely with clients to apply Quality by Design (QbD) principles and build seamless operational bridges with Contract Development and Manufacturing Organizations (CDMOs) across small molecules, large molecule biologics, cell and gene therapies, and advanced virology programs. Backed by a growth equity investment from Boston-based private equity firm Riverside Partners, Syner-G has expanded its international delivery capacity significantly through targeted integrations, including the acquisitions of Sequoia Biotech Consulting and RMC Pharmaceutical Solutions. Further driving innovation, in mid-2026 the firm launched 3D Intelligence (3Di), a people-centered artificial intelligence transformation service tailored specifically to streamline biopharma documentation and development workflows. Consistently recognized by BioSpace as one of the industry's premier workplaces, the organization is headquartered in Framingham, Massachusetts, and leverages a global, distributed network of over 400 specialized bio-pharmaceutical consultants, engineers, and regulatory compliance strategists across North America, Europe, and the Asia-Pacific region.

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