{"id":2362854,"url":"https://alion.io/job/us-worldmeds-quality-control-microbiology-associate","title":"Quality Control Microbiology Associate","company":{"id":2540669,"name":"US WorldMeds","domain":"usworldmeds.com","url":"https://alion.io/company/usworldmeds","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"ADP","truth_index":null},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Philadelphia, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":54000,"max_usd":116000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":870},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false}],"status":"live","first_seen_at":"2026-09-30T17:42:00Z","employer_posted_date":"2026-09-30","last_verified_at":"2026-10-23T16:47:45Z","board_verified":true,"closed_at":null,"days_open":23,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":23},"description":"SUMMARY:\nThe Quality Control Microbiology Associate will support the safety, quality, and compliance of drug products through the execution of routine microbiological testing and monitoring activities. This position is responsible for performing in-process environmental monitoring of cGMP manufacturing suites, conducting finished product safety testing including endotoxin and sterility assays, and assisting with stability program testing to evaluate product performance over time. The Associate will be expected to generate accurate and timely data while following SOPs, cGMP requirements, and regulatory guidelines. In addition, this role will support laboratory operations, assist with investigations and documentation activities, and collaborate with cross-functional teams to maintain high standards of product quality and patient safety.\nDUTIES AND RESPONSIBILITIES:\nPerform in-process environmental monitoring of classified cGMP manufacturing suites, including routine viable and non-viable particulate testing.\nExecute finished product microbiological assays such as endotoxin and sterility testing in accordance with compendial methods and internal SOPs.\nConduct stability testing to assess product quality and integrity throughout the product lifecycle.\nEnsure all laboratory activities are performed in compliance with cGMP, FDA, and other applicable regulatory requirements.\nAccurately document, analyze, and report test results in a timely manner while maintaining data integrity standards.\nParticipate in investigations related to environmental monitoring excursions, out-of-specification (OOS) results, or deviations, and support implementation of corrective and preventive actions (CAPA).\nCollaborate with cross-functional partners in Manufacturing, Quality Assurance, and Technical Operations to support batch release and regulatory submissions.\nMaintain laboratory equipment, supplies, and aseptic practices to ensure a safe, compliant, and efficient work environment.\nQUALIFICATIONS:\nBachelor’s or Associates degree in Molecular Biology, Biomedical Sciences, Microbiology, or a related field.\n0-3 years of experience working in a GMP-regulated quality control laboratory within the pharmaceutical or biotechnology industry.\nNovice working knowledge of cGMP regulations, USP, and EP testing requirements.\nKnowledge of microbiological techniques including rapid microbiology methods, endotoxin testing, growth promotion, plate reads, and environmental monitoring.\nAbility to perform or learn time-critical in-process and finished product testing to support manufacturing and clinical trial timelines.\nAbility to analyze and interpret data, prepare trending reports, and contribute to test method development and SOP revisions.\nStrong attention to detail, organizational skills, and commitment to data integrity and compliance.\nDESIRABLE\nHands-on experience with laboratory information management systems (LIMS) and electronic data capture tools such as MODA.\nPrevious Gown Qualification for aseptic processing experience.\nFamiliarity with continuous improvement initiatives, including updates to methods, SOPs, and workflows.\nExperience conducting laboratory investigations, preparing deviations, and supporting CAPA development.\nAbility to work independently on assigned projects with limited supervision.\nLimited knowledge and experience with EM plate reads, growth promotion as well as endotoxin and sterility testing.\nPHYSICAL DEMANDS:\nFrequently required to stand\nFrequently required to walk. \nFrequently required to sit. \nFrequently required to talk or hear. \nOccasionally required to lift light weights (less than 50 pounds) \nSpecific vision abilities required for this job include: close vision, color vision and ability to adjust or focus\nWORK ENVIRONMENT:\nThe noise level in the work environment usually is quiet.","description_format":"text","description_chars":3843,"description_truncated":false,"requirements":{"experience_years_min":null,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"associate","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Health Care","Prescription 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