Director, Compounding Program Management

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  and  For information on the company’s outstanding benefits, culture, and its talent‑first flexible/remote work approach, see below and visit

The Director, Compounding Program Management is a senior leader within the Compounding & Ops PMO, reporting to the Director, PMO.

This role is accountable for end‑to‑end program management across R&D, facilities, equipment, and compounding operations, supporting sterile and non‑sterile programs from concept through validation, launch, and sustained production readiness. The Director ensures that new products, processes, and technologies are not only scientifically sound, but operationally executable within regulated compounding environments.

The role plays a critical leadership function in new program implementation (NPI), including facility readiness, equipment procurement and qualification, cleanroom readiness, capacity planning, and site onboarding, ensuring seamless transition from development into routine compounding operations.

While Compounding leadership owns scientific direction and technical execution, this role ensures program discipline, operational alignment, and delivery predictability across formulation, process development, site & equipment readiness, validation, tech transfer, and manufacturing launch. This Director‑Level role will manage a growing team of non‑sterile and sterile R&D and NPI Program Managers.

This is a remote role with periodic travel (up to 50%) to sterile and non‑sterile compounding facilities and partner sites.

• Lead integrated program management for R&D, facilities, equipment, and compounding initiatives from concept through validation and operational launch.

• Own program plans that span formulation development, process scale‑up, facility readiness, equipment installation, qualification (IQ/OQ/PQ), and operational handoff.

• Ensure new programs are designed and executed with 503A & 503B sterile and non‑sterile operational realities in mind, including capacity, workflows, staffing, and compliance.

• Partner with internal and external Facilities, Engineering, Quality, R&D, Compounding, Legal, Recruiting, Training, Safety, and Operations teams to manage program timelines related to cleanroom buildouts, renovations, and capacity expansions.

• Oversee program management for equipment selection, procurement, installation, qualification, and integration into compounding workflows.

• Coordinate readiness across utilities, environmental controls, automation, and support systems required for sterile and non‑sterile compounding.

• Ensure facility and equipment milestones are fully integrated into overall program plans and launch decisions.

• Lead program execution for new product introductions (NPI), new dosage forms, new technologies, and site expansions.

• Drive alignment across R&D, Quality, Regulatory, Operations, and Supply Chain to ensure implementation readiness across people, process, equipment, and documentation.

• Facilitate structured go/no‑go decision‑making for validation, PPQ, and production start.

• Establish and manage program governance across a complex portfolio of sterile and non‑sterile initiatives.

• Identify and proactively mitigate risks related to facility constraints, equipment readiness, validation timelines, and regulatory compliance.

• Ensure all programs align with USP , , ,…