hims & hers
Quality Systems Lot Disposition Specialist
hims & hers, Gilbert, Arizona, United States, 85233
Overview
Join to apply for the
Quality Systems Lot Disposition Specialist
role at
hims & hers . This role is part of the Quality Unit in Apostrophe Pharmacy and plays a critical role in ensuring that all compounded products meet company and regulatory standards before release. The role places a heavy emphasis on documentation surrounding batch issuance, review, filing, and escalation of events, and supports the QS Manager in daily operations. The QS Lot Disposition Specialist ensures compliance with USP standards, cGMP requirements, and internal SOPs while safeguarding patient safety. Base pay range : $30.00/hr - $40.00/hr You Will
Manage batch record issuance, review, and final disposition of compounded lots. Perform detailed review of executed batch records to ensure accuracy, completeness, and compliance with cGMP and internal procedures. This includes scanning, filing, and archiving site documents in both digital and physical systems. Audit documentation for compliance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available). Support the design and enhancement of quality system tools and workflows, ensuring alignment with regulatory requirements and business needs. Ensure timely filing and archival of batch-related documentation to support audit readiness. Participate in the escalation, investigation, and closure of deviations, OOS results, and discrepancies, ensuring timely investigation and resolution. Collaborate with Production, Pharmacy, QC, and Inventory teams to ensure smooth lot disposition activities. Provide reports, trending data, and metrics to QS management to identify patterns and continuous improvement opportunities. Support internal and external audits by providing documentation and evidence related to lot disposition. Participate in drafting and revising SOPs, work instructions, and protocols relating to lot disposition. GDP additions Label issuance You Have
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. Strong understanding of USP standards, FDA 21 CFR Parts 210 & 211, and cGMP. GDP and GLP practices preferred. Excellent attention to detail, documentation practices, and organizational skills. Experience with investigations, deviation management, and escalation procedures. Proficiency in Google Workspace and familiarity with quality systems software. Strong interpersonal and communication skills (written and verbal). Pharmacy Technician or trainee license or willingness to acquire. Our Benefits
Competitive salary & equity compensation for full-time roles Unlimited PTO, company holidays, and quarterly mental health days Comprehensive health benefits including medical, dental & vision, and parental leave Employee Stock Purchase Program (ESPP) 401k benefits with employer matching contribution Offsite team retreats Equal Opportunity & Accessibility
Hims & Hers is an equal opportunity employer. We consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. We provide reasonable accommodations for qualified individuals with disabilities in our job application procedures. If you need assistance or an accommodation due to a disability, please contact accommodations@forhims.com. For more information on how we collect, use, retain, and disclose Personal Information, please refer to our Global Candidate Privacy Statement.
#J-18808-Ljbffr
Join to apply for the
Quality Systems Lot Disposition Specialist
role at
hims & hers . This role is part of the Quality Unit in Apostrophe Pharmacy and plays a critical role in ensuring that all compounded products meet company and regulatory standards before release. The role places a heavy emphasis on documentation surrounding batch issuance, review, filing, and escalation of events, and supports the QS Manager in daily operations. The QS Lot Disposition Specialist ensures compliance with USP standards, cGMP requirements, and internal SOPs while safeguarding patient safety. Base pay range : $30.00/hr - $40.00/hr You Will
Manage batch record issuance, review, and final disposition of compounded lots. Perform detailed review of executed batch records to ensure accuracy, completeness, and compliance with cGMP and internal procedures. This includes scanning, filing, and archiving site documents in both digital and physical systems. Audit documentation for compliance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available). Support the design and enhancement of quality system tools and workflows, ensuring alignment with regulatory requirements and business needs. Ensure timely filing and archival of batch-related documentation to support audit readiness. Participate in the escalation, investigation, and closure of deviations, OOS results, and discrepancies, ensuring timely investigation and resolution. Collaborate with Production, Pharmacy, QC, and Inventory teams to ensure smooth lot disposition activities. Provide reports, trending data, and metrics to QS management to identify patterns and continuous improvement opportunities. Support internal and external audits by providing documentation and evidence related to lot disposition. Participate in drafting and revising SOPs, work instructions, and protocols relating to lot disposition. GDP additions Label issuance You Have
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. Strong understanding of USP standards, FDA 21 CFR Parts 210 & 211, and cGMP. GDP and GLP practices preferred. Excellent attention to detail, documentation practices, and organizational skills. Experience with investigations, deviation management, and escalation procedures. Proficiency in Google Workspace and familiarity with quality systems software. Strong interpersonal and communication skills (written and verbal). Pharmacy Technician or trainee license or willingness to acquire. Our Benefits
Competitive salary & equity compensation for full-time roles Unlimited PTO, company holidays, and quarterly mental health days Comprehensive health benefits including medical, dental & vision, and parental leave Employee Stock Purchase Program (ESPP) 401k benefits with employer matching contribution Offsite team retreats Equal Opportunity & Accessibility
Hims & Hers is an equal opportunity employer. We consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. We provide reasonable accommodations for qualified individuals with disabilities in our job application procedures. If you need assistance or an accommodation due to a disability, please contact accommodations@forhims.com. For more information on how we collect, use, retain, and disclose Personal Information, please refer to our Global Candidate Privacy Statement.
#J-18808-Ljbffr