Hims and Hers Manager, Technical Services at Hims and Hers leads site-level technical activities including process verification, cleaning validation, and technology transfer. The role supports manufacturing reliability and process optimization.
Responsibilities
Hims & Hers is scaling a multi-site sterile and nonsterile manufacturing network spanning 503A compounding pharmacies, a 503B outsourcing facility, and a peptide active pharmaceutical ingredient (API) manufacturing site. The Manager, Technical Services is the site-level technical owner responsible for executing process verification, cleaning validation, and technology transfer activities, driving process optimization, and resolving equipment and process issues at their assigned facility. This role reports to the Director, Technical Services and works closely with site Operations, Quality, Engineering, and Maintenance to keep manufacturing running reliably day to day, while supporting process development, capital equipment installation, equipment qualification, and requalification work as the site grows.
Process Verification
Execute process verification activities for compounded preparations and manufacturing processes at the site, confirming that critical process parameters and in-process controls are consistently met.
Author and execute process verification protocols and reports, and maintain supporting data packages for audit and inspection readiness.
Flag process drift or emerging trends to site leadership and the Director, Technical Services, and recommend corrective action.
At sterile sites, plan and execute site-level aseptic process simulations (media fills) in line with network standards set by the Director, Technical Services, and support any related investigations.
Cleaning Validation
Execute the site's cleaning validation program, including cleaning method verification, swab and rinse sampling, and acceptance limit checks for compounding, filling, and processing equipment.
Author and execute cleaning validation protocols and reports, and manage the ongoing cleaning verification/monitoring schedule for the site.
Assess the cleaning validation impact of new products, equipment changes, or campaign changes at the site, and escalate revalidation needs to the Director, Technical Services.
Support and execute technology transfer of new products, formulations, and processes into the site, including transfers from R&D or from other manufacturing sites.
Coordinate site-level activities against transfer protocols, ensuring critical process parameters and acceptance criteria are met during transfer runs.
Qualification
Bachelor's degree in EngineeringWorking knowledge of USPStrong technical writing skillsExperience with peptideHands-on experience with autoclaves
Required
Bachelor's degree in Engineering, Pharmacy, Chemistry, or a related technical/scientific field required.
5+ years of experience in pharmaceutical manufacturing or sterile/nonsterile compounding, with hands-on experience in process verification, cleaning validation, technology transfer, or equipment troubleshooting.
Prior experience supervising or leading technical staff, including hiring, coaching, and performance management, in a regulated manufacturing or compounding environment.
Working knowledge of USP , , and (as applicable to site), FDA's Process Validation Guidance (2011), and cGMP requirements.
Experience supporting root-cause investigations and CAPA in a regulated manufacturing environment.
Strong technical writing skills, with the ability to author clear, defensible protocols and reports.
Comfort working hands-on with manufacturing equipment and collaborating cross-functionally with Operations, Quality, and Engineering.
Preferred
Experience with peptide, oligonucleotide, or other complex API manufacturing processes.
Hands-on experience with autoclaves, isolators, filling lines, or API processing/purification equipment.
Experience supporting new equipment commissioning, IOQ/PQ execution, or site launch activities.
Prior experience supporting FDA or state board of pharmacy inspections.