{"id":1929796,"url":"https://alion.io/job/curia-global-quality-control-analyst-iii","title":"Quality Control Analyst III","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":"A","score":89,"open_postings":16,"ghost_share":0,"stale_share":0.25,"repost_share":0,"time_to_fill_p50_days":74,"computed_at":"2026-10-21T05:46:15Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"middle","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":null,"salary_estimate":{"min_usd":56000,"max_usd":102000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":4013},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"Chromatography","optional":false},{"name":"GLP","optional":false},{"name":"GMP","optional":false},{"name":"HPLC","optional":false},{"name":"Mandiant capa","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-09-22T17:17:21Z","employer_posted_date":"2026-09-22","last_verified_at":"2026-10-21T17:48:59Z","board_verified":true,"closed_at":null,"days_open":29,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":29},"description":"Quality Control Analyst III in Rensselaer, NY - Day shift\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.\nBuild your future at Curia, where our work has the power to save lives\nCuria is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ 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 with matching contributions\nLearning platform\nAnd more!\nPosition overview\nThe Quality Control Analyst III is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples.\nTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.\nEssential job duties\nPerform complex testing and data evaluation such as TGA\nPerform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues\nParticipate in or assist with test method validations\nEvaluate data for trends\nSupport supervisors in OOS Investigations and complete CAPA requirements\nInteract with outside departments including attending meetings, providing updates, etc.\nCoordinate testing performed at outside testing labs, raw materials, etc.\nMaintain a detailed and accurate recording of activities and results on paperwork \nExecute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools\nTrain upon and understand methods, equipment and standard operating procedures\nProvide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures\nSupport equipment upkeep and laboratory method trouble shooting\nProvide technical assistance during the shift for test method trouble shooting\nPrepare and order supplies, as necessary\nEnter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management\nUtilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry\nInteract with other departments within the company for testing needs and scheduling\nMay lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams\nMay lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results\nEducation, experience, certification and licensures\nRequired\n· Bachelor's degree in Chemistry or related field\n· Minimum 5-7 year’s pharmaceutical experience or equivalent combination of education and experience\nPreferred\n· Experience working in cGMP or GLP pharmaceutical industry environment\nKnowledge, skills and abilities\nExcellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public\nAbility to meet deadlines and work under pressure with limited supervision\nStrong time management and organizational skills with the ability to multi-task and manage multiple projects independently \nAbility to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations \nAbility to write reports, business correspondence, and procedure manuals\nAbility to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations\nAbility to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis\nAbility to define problems, collect data, establish facts, and draw valid conclusions\nAbility to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables\nProficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems\nKnowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus\nThe above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel as classified. Management reserves the right to revise or amend duties at any time.\nPay Range: $84,000 - $95,000\nEducation, experience, location and tenure may be considered along with internal equity when job offers are extended.\nWe do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.\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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