Quality Systems Document Control Specialist

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 and 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.

We are looking for a Quality Systems Document Control Specialist to join our Quality Unit in XeCare Pharmacy. This role is responsible for supporting the document control system and lifecycle of controlled documents in a compounding pharmacy operating under 503A regulations. With a strong emphasis on Change Control support, SOP development, controlled issuance, review, filing, archival, and compliance tracking, the Document Control Specialist ensures that all documentation meets regulatory requirements and supports operational excellence.

• Support the administration of the Document Control System, ensuring proper management of controlled documents such as SOPs, batch records, logbooks, forms, policies, and protocols.

• Support the site level implementation of change controls and the impact to site documentation and defined processes.

• Support the design and enhancement of quality system tools and workflows, ensuring alignment with regulatory requirements and business needs.
  

• Issue and track SOPs and other controlled documents, ensuring only current, approved versions are in circulation.
  

• Assist in drafting, editing, and formatting SOPs, work instructions, and policies, ensuring clarity, consistency, and alignment with USP <795>, <797>, <800>, and FDA 21 CFR 210/211.
  

• Support SOP lifecycle management, including periodic review, approval workflows, revision history tracking, and retirement of obsolete versions.
  

• Support cross-functional SME reviews of SOPs and controlled documents, ensuring input from QA, Production, QC, and Compliance.
  

• Ensure timely training roll-out when new or revised SOPs are released, and maintain records to demonstrate compliance in alignment with the Training department and Operations teams.
  

• Maintain both electronic and physical filing systems, ensuring secure storage, easy retrieval, and audit readiness.
  

• Monitor document-related deviations, including missing signatures, uncontrolled copies, or outdated references, and escalate to QA Management for corrective action.
  

• Prepare and provide documentation packages for regulatory inspections and customer audits.
  

• Partner with QS Management to support continuous improvement of the document control process, including digitization initiatives and standardization projects.

• Bachelor’s degree preferred in a relevant discipline (science, quality, or engineering-related field) or equivalent combination of education and experience.

• 3+ years of related experience in quality, manufacturing, or a regulated industry may substitute for a degree.
  

• Hands-on experience with SOP drafting, formatting, and controlled documentation systems.
  

• In-depth knowledge of cGMP documentation practices, USP standards, and FDA record-keeping requirements.
  

• Exceptional attention to detail with strong editing, writing, and organizational skills.
  

• Familiarity with electronic document management systems (EDMS) or validated document control or quality management software.
  

• Strong collaboration skills, with the ability to work across QA, Production, and Compliance teams.