Senior Program Manager, Sterile Compounding (PMO)

Senior Program Manager, Sterile Compounding (PMO) Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve. Hims & Hers is a public company, traded on the NYSE under the ticker symbol “HIMS.” To learn more about the brand and offerings, you can visit hims.com/about http://hims.com/about and hims.com/how-it-works http://hims.com/how-it-works . For information on the company’s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals http://www.hims.com/careers-professionals. ABOUT THE ROLE: Hims & Hers is seeking a highly driven Senior Program Manager, Sterile Compounding to lead the end-to-end product development and launch processes for both (503B) (503A) sterile pharmaceutical products and facilities,. The ideal candidate will have deep experience in regulated environments, with a strong understanding of sterile manufacturing, product formulation, tech transfer, regulatory pathways, operational launch readiness, go-to-market readiness, and cross-functional collaboration. This role will drive projects from concept through R&D to launch, ensuring timelines, budgets, and quality standards are met. This role will support both the VP, Innovation and will be embedded within the fast-growing Operations & Innovation Program Management Office (PMO), reporting to the Director of Innovation Program Management (PMO). This role will be responsible for managing teams remotely as well as on-site. This is a remote role with regular travel up to 25% of the time. YOU WILL: - Lead cross-functional project teams through the full product development lifecycle of 503a and 503b sterile product launches – from ideation through R&D to commercial launch. - Lead say expansion and continuous improvement workstreams that support 503a and 503b sterile product development. - Build and maintain integrated project plans including key milestones, timelines, resource requirements, risks, and mitigation plans. - Prepare and present program updates to leadership and stakeholders, highlighting progress, risks, and mitigation strategies. - Maintain project documentation in accordance with internal procedures and regulatory requirements. - Drive decision-making, facilitate team meetings, and act as a key point of contact for all project-related activities. - Track budgets and resource allocation across multiple simultaneous product development initiatives. Roles & Responsibilities will include: End-to-End NPI Ownership: - Lead all phases of new product introduction (NPI) for all sterile compounded products, ensuring compliance with 503A & 503B regulations and internal quality standards. - Work closely with PMO PMs and SME PMs to ensure key deliverables such as packaging and marketing are being executed in time for launch. - Develop and optimize NPI processes for a growing & changing business. R&D and Analytical Development Coordination: - Oversee due diligence, formula development, and R&D - Align with formulation scientists and analytical chemists on method development, sample testing, and accelerated stability studies. - Track R&D milestones including pilot batches, formulation refinement, and compatibility testing. - Ensure timely execution of formulation, method development, process development, tech transfer, and equipment validation activities. Quality Partnership - Work closely with our Quality team & Quality PMs to ensure proper alignment and execution is followed throughout the proj ... (truncated, view full listing at source)