United States Pharmacopeia

Project Director, Health Product Stability and Climate Resilience (Rockville, MD - Hybrid Role)

United States Pharmacopeia$165K — $213K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Advanced degree in Pharmaceutical Sciences, Chemistry, Public Health, or a related field.
  • Minimum of 10 years of experience in pharmaceutical stability, regulatory compliance, and product lifecycle management.
  • Proven experience in implementation research and evidence generation related to health products and systems.
  • Deep expertise in pharmaceutical lifecycle management and real-world product performance monitoring.
  • Strong knowledge of ICH stability guidelines, GMP/cGMP frameworks, and relevant analytical methodologies.
  • Solid understanding of climate-related risks affecting health products and supply chains.
  • Experience working in low- and middle-income countries (LMICs).

Responsibilities

  • Provide overall leadership for project strategy across all countries and workstreams.
  • Ensure timely delivery of high-quality outputs and program milestones.
  • Oversee implementation across technical areas for quality and consistency.
  • Guide the development of implementation research related to health outcomes.
  • Oversee identification of innovations ensuring alignment with program objectives.
  • Serve as liaison with donors, authorities, and stakeholders for effective communication.
  • Foster strong relationships with partners, monitor performance, and address risks.

Benefits

  • Company-paid time off and comprehensive healthcare options.
  • Retirement savings plans for long-term financial security.
Full Job Description
Brief Job Overview

The Project Director provides strategic, technical, and operational leadership for a multi-country program addressing the impact of climate change on the stability and performance of critical health products. This role is accountable for overall program vision, execution, and results, ensuring high-quality delivery in alignment with donor expectations and global health priorities. The Project Director leads a multidisciplinary team of technical experts and serves as the primary liaison with donors, governments, and global partners. The role emphasizes strategic direction, partnership development, and translation of evidence into scalable solutions and global impact.

The Project Director, Safeguarding Heat Stability in Essential Life -Saving Drugs and Diagnostics (SHIELD) has the following responsibilities:

Project Leadership and Results Delivery
  • Provide overall leadership for the project strategy, implementation, and results across all countries and workstreams.
  • Ensure timely delivery of high-quality outputs and achievement of the program milestones in line with program requirements and organizational standards.
  • Oversee implementation across technical areas, ensuring coordination, quality, and consistency.

Technical Strategy and Innovation
  • Provide strategic oversight of technical activities related to health product stability, evidence generation, and climate resilience.
  • Guide the development and execution of implementation research and evidence generation, ensuring relevance to health outcomes and policy.
  • Oversee identification and advancement of promising solutions and innovations, ensuring alignment with program objectives and scalability potential.
  • Ensure technical rigor and adherence to international standards by leading specialized technical teams.

Stakeholder Engagement and Partnerships
  • Serve as the primary liaison with donors, local and regional authorities, and global stakeholders, ensuring effective communication, alignment, and reporting.
  • Represent the project in global, regional, and national forums, contributing to thought leadership and knowledge exchange.
  • Lead a global consortium of partner organizations across Europe, Asia, Africa, and Latin America, ensuring effective coordination, clear governance structures, aligned workplans, and consistent communication.
  • Foster strong, collaborative relationships, monitor partner performance and compliance with contractual obligations, and proactively address risk to maintain high-quality program delivery.

Program management and Operations
  • Ensure strong project management systems, including planning and performance tracking.
  • Ensure compliance with contractual requirements and organizational policies to maintain financial, technical, and operational integrity.
  • Establish efficient operational structures and processes to support multi-country implementation.

Knowledge Management & Dissemination
  • Ensure generation, documentation, and dissemination of high-quality, evidence-based knowledge products.
  • Promote learning and uptake of findings to inform global policy, practice, and future investments in climate-resilient health products.

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, and the ability to quickly build credibility with stakeholders, along with the following competencies and experience:
  • Advanced degree in Pharmaceutical Sciences, Chemistry, Public Health, or a related field.
  • Minimum of 10 years of experience in pharmaceutical stability, regulatory compliance, and product lifecycle management.
  • Demonstrated expertise in developing and managing stability studies, regulatory submissions, and data systems supporting product quality and performance.
  • Proven experience in implementation research and evidence generation related to health products and systems.
  • Deep expertise in pharmaceutical lifecycle management and real-world product performance monitoring.
  • Strong knowledge of ICH stability guidelines, GMP/cGMP frameworks, and relevant analytical methodologies.
  • Solid understanding of climate-related risks affecting health products and supply chains.
  • Proven track record leading large, complex, multi-country programs, with full accountability for results.
  • Demonstrated leadership in matrixed environments and ability to manage diverse, cross-functional teams and stakeholders.
  • Experience working in low- and middle-income countries (LMICs).
  • Excellent communication, negotiation, and cross-cultural collaboration skills.


Additional Desired Preferences
  • Advanced degree in Pharmaceutical Sciences, Chemistry, Public Health, or related field.
  • Familiarity with the prevention, diagnosis, and treatment of HIV, Malaria, PPH, and TB, and decentralized care models

Supervisory Responsibilities

This is a supervisory role.

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 $165,521.00 - $213,700.00 annually. (

Compensation within this range is determined based on experience, qualifications, and alignment with internal and external benchmarks.)

Target Annual Bonus: % 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.

About United States Pharmacopeia

The United States Pharmacopeia (USP) is a pharmacopeia (compendium of drug information) for the United States published annually by the United States Pharmacopeial Convention (usually also called the USP), a nonprofit organization that owns the trademark and also owns the copyright on the pharmacopeia itself. The USP is published in a combined volume with the National Formulary (a formulary of medicines authorized for prescription by US federal agencies) as the USP-NF. The USP-NF is a combination of two official compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). It contains standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical devices, dietary supplements, and other therapeutics. The USP-NF is a recognized authority in the United States and other countries. The USP's focus on quality standards for medicines, dietary supplements, and food ingredients helps to ensure the quality of these products and their ingredients.
Learn more about United States Pharmacopeia
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