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New Albany, Ohio, United States
Onsite
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.
The Sterile Technical Services (TS) Engineer is responsible for the design, qualification, validation, optimization, and lifecycle support of aseptic compounding processes, facilities, and equipment used in the production of sterile drug products. This role ensures sustained compliance with USP <797>, applicable FDA and cGMP requirements, and internal quality standards, while driving continuous improvement in sterility assurance, process robustness, and operational efficiency.
The position works cross-functionally with Operations, Quality, Validation, Microbiology, and Maintenance teams to support routine manufacturing, new product introductions, technology transfers, and regulatory inspections.
Work Environment
Work performed in ISO-classified cleanrooms and controlled environments, requiring gowning and aseptic behaviors
Office-based engineering, documentation, and analysis work
Occasional off-hours or on-call support for manufacturing operations and critical activities
Aseptic Process & Equipment Engineering
Design, implement, and maintain aseptic compounding and sterile processing operations for sterile drug products.
Support selection, installation, qualification, and lifecycle management of aseptic compounding equipment, including cleanroom systems and utilities.
Lead or support IQ/OQ/PQ activities for equipment, facilities, and processes in regulated environments.
Provide engineering support for ISO-classified cleanrooms, HVAC systems, and critical utilities impacting sterility assurance.
Sterility Assurance & Regulatory Compliance
Ensure compliance with USP <797> (and USP <800>, where applicable), FDA regulations, and cGMP requirements.
Author, review, and approve SOPs, validation protocols, risk assessments, and technical reports.
Support and participate in media fills, environmental monitoring programs, gowning qualifications, and aseptic process simulations.
Lead or support contamination investigations, deviation management, and CAPA development.
Process Optimization & Troubleshooting
Investigate aseptic process deviations and equipment failures using structured root cause analysis.
Apply risk management tools (e.g., FMEA) to identify and mitigate risks to sterility assurance.
Drive continuous improvement initiatives to improve process robustness, yield, throughput, and compliance.
Support remediation activities related to audits, inspections, or internal quality findings.
Cross-Functional Collaboration
Partner closely with Compounding Operations, Quality Assurance, Validation, Microbiology, Facilities, and Maintenance.
Provide technical support during regulatory inspections and audits, including FDA inspections and audit responses.
Support technology transfer, scale-up, and new product introductions, including process readiness and validation planning.
Documentation, Training & Knowledge Management
Maintain compliant, inspection-ready engineering and validation documentation.
Train operations and technical staff on aseptic principles, equipment operation, contamination control, and best practices.
Stay current with evolving regulatory guidance, industry standards, and emerging aseptic technologies.
Bachelor’s degree in Engineering, Pharmaceutical Sciences, Pharmacy, or a related technical field.
1-3+ years of experience in aseptic or sterile compounding, pharmaceutical manufacturing, or regulated cleanroom environments.
Working knowledge of cGMP, USP <797> (and <800> where applicable), and aseptic processing principles.
Hands-on experience with aseptic compounding, sterilization methods (e.g., steam, dry heat, filtration), and cleanroom operations.
Experience supporting equipment qualification, process validation, and lifecycle management in regulated environments.
Preferred Qualifications
Master’s degree in Engineering or Pharmaceutical Sciences.
Experience with isolators, RABS, single-use systems, or advanced aseptic automation.
Lean, Six Sigma, or formal risk management training.
Direct experience supporting FDA inspections, regulatory audits, or inspection remediation activities.
Key Competencies
Strong technical problem-solving and analytical skills
High attention to detail with a focus on data integrity and documentation excellence
Effective cross-functional communication and collaboration
Ability to operate in fast-paced, highly regulated environments
Strong commitment to quality, safety, and patient protection
Competitive salary & equity compensation for full-time roles
Comprehensive health benefits including medical, dental & vision, and parental leave
Employee Stock Purchase Program (ESPP)
401k benefits with employer matching contribution
Conditions of Employment:
This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown and other items as required.
This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR).
Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve hour shift. Must be able to lift up to 50lbs.
Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs.
We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply—even if you're not sure if your background or experience is a perfect match.
Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.
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