Production Laboratory Technician

Overview Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview This onsite position supports USP’s microbiology operations manufacturing function within the microbiology business unit. The incumbent will work with the team primarily focused on the production and support tasks related to the production of microbial Analytical Reference Materials (ARMs) and reference standards. Successful applicants will anticipate and solve problems within their area of responsibility, keep meticulous records, and have good communication skills. Impact at USP As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Production Laboratory Technician Has The Following Responsibilities Reference Material Production: Directly engage in hands-on production activities of USP Analytical Reference Material. Perform microbial reference material production activities according to established SOPs. Perform incubations, serial dilutions and enumeration of microbial samples. Prepare materials for production including sterilizing components, preparing media, assembling component packaging, and material qualification. Ensure equipment is properly calibrated, maintained, and operated according to SOPs and test methods. Ensure production space is properly cleaned and maintained according to SOPs to ensure quality of production events. Fulfillment of finished goods Analytical Reference Material products. Documentation & Compliance: Ensure meticulous and accurate documentation of all relevant paperwork. Adhere to all regulatory compliance regulations for good documentation practices. Ensure robust record keeping for production activities. Update logs and categorize documents. Assist QA/QC with production investigations. Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, a commitment to excellence through inclusive and equitable behaviors and practices, and the ability to quickly build credibility with stakeholders. The following competencies and experience are preferred: Bachelor’s or associate’s degree in microbiology or a relevant field. 1–3 years of relevant microbiology experience. Proficient in Excel, Word, PowerPoint software applications. Additional Desired Preferences Experience related to microbiology or biological science. Biological production experience. Manufacturing experience in a controlled environment. Laboratory experience, including pipetting and aseptic technique. Understanding of ISO 9001/ISO 17034, and ISO 17025. Knowledge of USP Compendia (Monographs, General Chapters). Knowledge of FDA regulations, other Compendia, and ICH guidelines. Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Compensation Base Hourly Range: USD $29.54 – $36.87 per hour. Target Annual Bonus: Varies based on level of role. Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons. Note USP does not accept unsolicited resumes from third-party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Equal Opportunity Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities. This employer is required to notify all applicants of their rights pursuant to federal employment laws. 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