The U.S. Pharmacopeial Convention (USP) logo

Senior Director, Global Manufacturing Programs

The U.S. Pharmacopeial Convention (USP)

Rockville, MDFull-time$201–286K/yrPosted 3mo agoSeen in employer's feed 3 days ago

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At a glance

Compensation
$201–286K/yr
Location
Rockville, MD
Schedule
Full-time
Work Authorization
US work authorization required

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Requirements

Credentials this posting asks for.

Doctorate

Job overview

The U.S. Pharmacopeial Convention (USP) is hiring a Senior Director, Global Manufacturing Programs. The Senior Director, Global Manufacturing Programs will provide end-to-end technical leadership for MedSuRe and other manufacturing programs, ensuring alignment with program strategies and donor objectives. This role involves overseeing technical execution, establishing standards, mitigating risks, and driving continuous improvement. The director will also translate strategies into actionable plans, ensure quality and compliance, and represent the organization in external engagements. Additionally, they will lead and mentor multidisciplinary teams, fostering collaboration and high performance.

Key focus areas include Provide end-to-end technical leadership on MedSuRe and other assigned programs, Oversee technical execution through matrixed teams, ensuring delivery against milestones, and Establish and uphold technical standards, governance frameworks, and best practices.

Successful candidates bring Advanced Degree In Pharmaceutical Sciences, Chemistry, Public Health, Or Related Field, 12+ Years Experience In Pharmaceutical, Biotech, Or Advanced Manufacturing, and Leadership Experience Within Pharmaceutical, Biotech, Or Advanced Manufacturing Environments. Important skills include Technical Leadership, Technical Direction Setting, Technical Execution Oversight, Technical Standards Establishment, Governance Frameworks, and Best Practices. Preferred (not required): Understanding Of LMIC Challenges and Operating Contexts In LMICs.

Skills & qualifications

RequiredNice to have

Skills

Technical LeadershipTechnical Direction SettingTechnical Execution OversightTechnical Standards EstablishmentGovernance FrameworksBest PracticesRisk MitigationTechnical Performance MonitoringContinuous ImprovementStrategic ExecutionPortfolio IntegrationProgram PrioritizationResource PlanningQuality StandardsComplianceStakeholder ManagementDonor CommunicationsTechnical Strategies DevelopmentLeadershipCoachingTechnical GuidanceAccountabilityCollaborationHigh PerformanceScientific IntegrityRegulatory ExcellenceEvidence-Based Decision-MakingEquitable Management PracticesUnderstanding of Drug DevelopmentUnderstanding of Commercialization ProcessesUnderstanding of Manufacturing ProcessesTechnology TransferScale-UpProcess ValidationRegulatory Approval PathwaysRoute-to-Market StrategiesManaging RiskManaging DependenciesManaging Technical ComplexityAligning Diverse StakeholdersCoordinating Multiple WorkstreamsStrong Stakeholder ManagementExecutive CommunicationConflict ResolutionDriving AlignmentUnderstanding of LMIC ChallengesOperating Contexts in LMICs

Qualifications

Advanced Degree in Pharmaceutical SciencesAdvanced Degree in ChemistryAdvanced Degree in Public HealthAdvanced Degree in Related Field12+ Years Experience in Pharmaceutical EnvironmentLeadership ExperienceExperience Leading Complex Programs or PortfoliosExperience Leading Cross-Functional Matrixed TeamsExperience in Relevant LMIC Markets

Benefits

Paid Time Off
Medical Insurance
401(k) Match

Full job description

Description

How will YOU create impact here at USP?

As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.

Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.

The Senior Technical Director, Global Manufacturing Programs has the following responsibilities:

Technical Leadership and Delivery:

  • Provide end-to-end technical leadership on MedSuRe and other assigned programs across manufacturing programs, setting technical direction and ensuring alignment with approved program strategies and donor objectives.

  • Oversee technical execution through matrixed teams, ensuring delivery against milestones, quality standards, and performance expectations.

  • Establish and uphold technical standards, governance frameworks, and best practices to ensure consistency, rigor, and scalability across programs.

  • Proactively identify, assess, and mitigate risks, escalating critical issues to the Department Head when necessary.

  • Monitor and report on technical performance, milestones, and risks, providing clear visibility to leadership.

  • Drive continuous improvement across technical approaches and delivery models to enhance efficiency and impact.

Strategic Execution and Portfolio Integration:

  • Translate organizational and donor-driven strategies into actionable program plans, including work plans, milestones, and resource alignment.

  • Ensure coherence and integration across technical workstreams to enable efficient, coordinated execution.

  • Contribute to program prioritization and resource planning in partnership with the Head of Global Pharmaceutical Programs.

  • Ensure all technical outputs meet high standards of quality, compliance, and relevance to global health manufacturing objectives.

Stakeholder Engagement and Representation:

  • Serve as a senior technical representative in engagements with donors, partners, and external stakeholders, leading or contributing to technical discussions and program reviews.

  • Support and, where appropriate, lead donor communications related to technical progress, performance, and risk management.

  • Represent the organization in external forums, positioning its technical expertise and advancing its reputation in global health manufacturing.

  • Lead or contribute to the development of technical strategies for proposals and new initiatives, ensuring alignment with organizational capabilities and market needs.

Team Leadership and Collaboration:

  • Lead and mentor multidisciplinary, geographically dispersed teams through matrixed structures, fostering accountability, collaboration, and high performance.

  • Provide technical guidance and coaching to strengthen the team's capabilities and ensure the consistent application of standards and best practices.

  • Promote a culture of rigor, continuous learning, and excellence across all technical and programmatic activities.

Who is USP Looking For?

The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:

  • Advanced degree (Ph.D. or MS) in Pharmaceutical Sciences, Chemistry, Public Health, or a related field.

  • Minimum of 12 years of experience, including leadership experience within pharmaceutical, biotech, or advanced manufacturing environments, with a strong understanding of drug development and commercialization processes.

  • Deep understanding of manufacturing processes, including technology transfer, scale-up, and process validation, as well as regulatory approval pathways, and route-to-market strategies within regulated environments.

  • Proven experience leading complex programs or portfolios, including managing risk, dependencies, and technical complexity across concurrent workstreams.

  • Demonstrated success leading cross-functional, matrixed teams, aligning diverse stakeholders, and coordinating multiple workstreams to deliver against shared objectives and timelines.

  • Strong stakeholder management and executive communication skills, translating technical work into clear impact narratives.

  • Ability to resolve conflicts and drive alignment across senior technical teams.

  • Understanding of the challenges and operating contexts associated with low- and middle-income countries (LMICs), with experience in, or exposure to, relevant markets considered a plus.

Supervisory Responsibilities: Yes.

Benefits

USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.

Compensation

Base Salary Range: USD $200,812.00 – $286,157.00 annually.

Target Annual Bonus: 13%/Varies based on role level.

Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons.

Note: USP does not accept unsolicited resumes from 3rd-party recruitment agencies and is not responsible for fees incurred by recruiters or other agencies, except under a specific written agreement with USP.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

This employer is required to notify all applicants of their rights pursuant to federal employment laws.

For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

Job Category Technical Programs

Job Type Full-Time

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