{"id":1929809,"url":"https://alion.io/job/curia-global-supervisor-quality-disposition","title":"Supervisor, Quality Disposition","company":{"id":2070902,"name":"Curia","domain":"curiaglobal.com","url":"https://alion.io/company/curiaglobal","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Oracle","truth_index":{"grade":"B","score":75,"open_postings":17,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-10-14T06:34:16Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Rensselaer, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":102000,"max":128000,"currency":"USD","period":"year","gross":null,"usd_annual":128000},"salary_estimate":null,"experience_years_min":6,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-06-01T20:50:38Z","employer_posted_date":"2026-06-01","last_verified_at":"2026-10-14T14:05:28Z","board_verified":true,"closed_at":null,"days_open":134,"trust":{"level":"stale","repost_count":0,"flags":["stale"],"days_open":134},"description":"Quality Disposition Supervisor in Rensselaer, NY\nOur Rensselaer site is undergoing a crucial quality transformation. This is a rare opportunity to join a highly visible project, re-engineer quality systems from the ground up, and gain unmatched regulatory exposure.\nThe Quality Disposition Supervisor will be responsible for the disposition of intermediates, API’s and incoming materials. This role will require leading the team responsible for batch dispositions and will also lead the site disposition reviews to meet supply commitments. Acts as a primary gate keeper for the disposition process at the site, ensuring batch record reviews are completed in a compliant manner, all deviations impacting the disposition are closed, QC data is reviewed per the procedures, all open change controls and CAPAs tied to the batch disposition are assessed and impact is documented. Ensures the breakdown/demand maintenance workorders impacting the batch are reviewed prior to the disposition and Quality impact assessment is documented.\nBuild your future at Curia, where our work has the power to save lives\nWe proudly offer:\nGenerous benefit options (eligible first day of employment) \nPaid training, vacation and holidays (vacation accrual begins on first day of employment)\nCareer advancement opportunities \nEducation reimbursement\n401k program\nLearning platform\nAnd more!\nEssential Duties and Responsibilities:\nActs as the point of contact for product disposition\nBe able to objectively and comprehensively review disposition packages and drive Quality decisions related to product disposition based on data, strong technical & scientific rationale, data integrity requirements, compliant to regulatory and site procedural requirements\nResponsible for ensuring batch records have been thoroughly reviewed before product disposition to the customer within established timelines\nResponsible for closure of Deviations, CAPAs, Change Controls, and Customer Complaint Investigations related to CURIA-New York client products \nInterfaces with the cross functional departments to resolve any comments from the batch record reviews in a compliant manner \nKey point of contact for addressing product disposition related questions in customer audits and regulatory inspections\nWill act as subject matter expert for all quality issues related to batch release\nWill be responsible to develop Quality disposition and batch record reviewer qualification program\nPlay a key role in creating training feedback loop from batch records reviews with manufacturing and other cross functional teams to drive continuous improvements\nEducation and Experience:\nBachelor’s degree in science or related study\nMinimum of six (6) years of GMP experience in an FDA regulated pharmaceutical environment including minimum of four (4) years of experience in a Quality disposition reviews in a supervisory role\nSupervisory Responsibilities:\nThis role has supervisory responsibilities, involves mentoring, guiding, and advising.\nOther Skills and Abilities:\nLeads with integrity and respect\nProvides guidance, coaching, and mentorship to team members, sitewide\nDemonstrates business acumen\nFosters a collaborative and positive work environment\nChampions change\nCoaches and Develops\nPromotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.\nDemonstrates strong attention to detail\nAbility to work promptly and under pressure to meet customer and business deadlines associated with batch record lot release\nOther Qualifications:\nMust pass a background check\nMust pass a drug screen \nMay be required to pass Occupational Health Screening\nPay Range: $102,000-$128,000/yr\nAll interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. 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