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Cmc Program Manager Jobs in Fort Washington, MD (NOW HIRING)

Perks: Full and comprehensive benefits program, 24 days of paid vacation/holidays in your first ... CMAC, CMC) preferred. * Travel: Must have reliable transportation and be able to travel to and ...

Perks: Full and comprehensive benefits program, 24 days of paid vacation/holidays in your first ... CMAC, CMC) preferred. * Travel: Must have reliable transportation and be able to travel to and ...

... programs as needs. * Completes documentation associated with manufacturing processes (e.g. batch ... Establishing documentation management systems for CMC development and meeting FDA GMP, regulatory ...

Joint Logistics SME 043-26

Arlington, VA · On-site

$150K - $175K/yr

... management, systems and analysis. We are seeking a Joint Logistics SME who will thrive in a ... programs and LP Branch support to the Joint Directorates and coordination with the other service HQ'

Showing results 41-58

Cmc Program Manager information

See Fort Washington, MD salary details

$39.7K

$110.7K

$161.7K

How much do cmc program manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for cmc program manager in Fort Washington, MD is $110,690.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,900.00 and $136,500.00 per year, depending on experience, location, and employer.

What is a CMC Program Manager?

CMC Program Managers are professionals responsible for overseeing the Chemistry, Manufacturing, and Controls (CMC) aspects of pharmaceutical or biotechnology product development. They coordinate cross-functional teams to ensure that drug development activities related to product formulation, manufacturing, quality, and regulatory submissions are completed on time and within budget. Their role is crucial in advancing products through clinical development to commercialization while ensuring compliance with global regulatory requirements.

What are the key skills and qualifications needed to thrive as a CMC Program Manager?

To thrive as a CMC Program Manager, you need expertise in chemistry, manufacturing, and controls (CMC), project management experience, and an advanced degree in life sciences or a related field. Familiarity with regulatory submission systems, quality management tools, and certifications such as PMP or Six Sigma are highly valued. Strong leadership, cross-functional communication, and problem-solving skills help manage diverse teams and complex projects effectively. These skills ensure the successful development, regulatory compliance, and timely delivery of pharmaceutical products.

What are some typical challenges a CMC Program Manager faces when coordinating cross-functional teams?

A CMC Program Manager often encounters challenges in aligning the goals and timelines of diverse teams such as process development, analytical, regulatory, and manufacturing. Communication gaps and shifting priorities can complicate project execution, especially when managing external partners or contract manufacturing organizations. Proactive stakeholder engagement and clear documentation are essential to ensure that everyone remains on track and regulatory requirements are met. Successfully navigating these complexities is key to advancing products efficiently through the development pipeline.

What is the difference between Cmc Program Manager vs Cmc Project Manager?

AspectCmc Program ManagerCmc Project Manager
CredentialsTypically requires a Bachelor's degree in life sciences, engineering, or related field; often certifications like PMP or PgMPUsually holds a Bachelor's degree in a relevant field; PMP certification is common
Work EnvironmentOversees multiple projects within a program, coordinating cross-project activities in biotech or pharma industriesManages individual projects, focusing on specific deliverables within the CMC scope
Employer & IndustryPharmaceutical, biotech, or life sciences companies managing complex product developmentSimilar industry, often within the same companies, focusing on specific project execution

The Cmc Program Manager oversees multiple related projects, ensuring alignment with strategic goals, while the Cmc Project Manager focuses on executing individual projects within the CMC domain. Both roles require similar credentials and work in the same industry, but differ in scope and responsibilities.

What job categories do people searching Cmc Program Manager jobs in Fort Washington, MD look for?

The top searched job categories for Cmc Program Manager jobs in Fort Washington, MD are:

Infographic showing various Cmc Program Manager job openings in Fort Washington, MD as of June 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $110,690 per year, or $53.2 per hour.

Regulatory Affairs Business Unit Leader

BIOLOGICS CONSULTING GROUP INC

Alexandria, VA • On-site

$170 - $195/hr

Other

This job post has expired today. Applications are no longer accepted.


Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Regulatory Affairs Business Unit Leader

Regular Full-Time Management US

2 days ago Requisition ID: 1077

Salary Range: $170,000.00 To $195,000.00 Annually

Regulatory Affairs Business Unit Leader

(RA Strategy and Project Management)

Position Summary:

The role includes leading the Regulatory Affairs team, responsibility for all team financial KPIs, and providing knowledge, experience, business development support, and direction to achieve company and business unit goals. The incumbent will foster a collaborative, team-oriented environment, ensuring an overall ‘culture of quality’ in the execution of services provided to clients. The Business Unit Leader is responsible for driving performance, achieving goals, and advancing growth strategies. This position requires a balance of client/opportunity oversight, quality management, and people management, along with strategic business development and marketing acumen, with support from regulatory affairs team members, in line with the Company's growth objectives as defined by Management (65% of time).Billable/consulting duties (35% time) will include providing direct client consultation and delivering high-level strategic thinking with operational execution across all stages of product development, registration, and post-marketing.

This individual will lead a team of strategic regulatory experts and experienced operational regulatory project managers at all levels. The team primarily supports large cross-functional projects that engage specialists from other business units, including CMC, clinical, nonclinical, regulatory operations, and medical devices, as well as external partners.

Biologics Consulting Group, Inc. works with medical devices, biologics, and pharmaceutical companies to advance patient health.

Responsibilities:

  • Lead and mentor a team of regulatory affairs strategy and project managers with a focus on high-quality and timely delivery of regulatory submissions spanning INDs, BLAs, NDAs, etc.
  • Develop and execute an annual strategic business plan for the regulatory affairs consulting practice, ensuring alignment with company goals
  • Identify new business opportunities, expand the customer base, and build long-term client relationships
  • Monitor industry trends, regulatory changes, and emerging market needs to keep services relevant and competitive
  • Serve as the primary point of contact for key clients, providing expert guidance on complex regulatory strategies
  • Lead client presentations, negotiations, and communications to maintain high levels of satisfaction and loyalty
  • Develop strategy and implement an action plan for capacity planning and growth, including recruitment.
  • Work with other team leaders to facilitate the timely identification of resources required to support single and multidisciplinary projects where appropriate
  • Collaborate with BD, HR, the Executive team and other group leaders in identifying best practices for onboarding, recruiting, staff growth and business development to meet business goals.
  • Demonstrated leadership ability including ability to create a positive and collegial culture and motivate the regulatory affairs team to perform effectively
  • Facilitate successful project/program launches while ensuring that the programs run smoothly and in compliance with agreed-upon timelines and budgets.
  • Lead the execution of regulatory plans, ensuring alignment between day-to-day operations and broader strategic objectives across global programs.
  • Identify and propose innovative regulatory pathways and planning scenarios that align with global regulatory expectations and business objectives.

Requirements:

  • Bachelor’s degree in a scientific, regulatory, or engineering discipline; an advanced degree is highly preferred.
  • Minimum of 10 years of progressive experience in the pharmaceutical, biotechnology, or related life sciences industry, with at least 5 years in a leadership role in regulatory strategy or regulatory program management
  • Proven ability to partner on regulatory strategy and lead execution across all stages of product development, including PIND/IND/BLA/MAA/NDA/ANDA submissions, global registration, and post-marketing activities
  • Deep understanding of U.S. regulatory requirements with working knowledge of international (ex-U.S.) regulations and agency expectations, including global regulatory pathways, expedited programs, and dossier structures.
  • Exceptional communication and influencing skills, with the ability to synthesize complex regulatory information and translate it into clear recommendations for senior leadership and global stakeholders.
  • Demonstrated ability to develop, implement, refine, and leverage project management tools and best practices to enhance visibility, efficiency, cross-functional alignment, and meeting effectiveness across regulatory affairs and project teams.
  • Demonstrated experience facilitating cross-functional team meetings, driving structured agendas, documenting decisions and actions, and maintaining strong meeting hygiene and team accountability in a matrixed environment.
  • Expert skills required for Smartsheet (Regulatory Activity and Submissions Project Plans) and Microsoft Office Suite
  • Expert in creating visuals using PPT generated from timeline integration tools (ie, One Pager, Office Timeline Pro, etc.)
  • Must exercise rapid learning ability, attention to detail, excellent computer skills, excellent oral and written communication skills, team player, organized analytical thinker with a high level of energy and self-motivation
  • Demonstrated versatility in conflict resolution, problem solving, and working effectively as part of a cross-functional organization.
  • Strategic thinking and problem-solving skills, with a strong focus on client satisfaction and business growth

Key Performance Indicators:

  • Contribution to team revenue and overall business development
  • Implementation of scalable project management system across team
  • Quality and timeliness of client deliverables
  • Strengths of client relationships and client satisfaction
  • Mentorship and development of junior and mid-level staff
  • Contributions to thought leadership and professional visibility
  • Demonstrated teamwork and leadership capabilities

Proficient in Microsoft Office Suite, keyboarding skills, strong documentation skills, math aptitude, diplomacy and leadership skills, professionalism, time management, ability to multitask, able to work independently as well as collaboratively, and able to maintain confidentiality.

The listed requirements are representative of the knowledge, skills, and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

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