{"id":1682889,"url":"https://alion.io/job/ccrm-omniabio-quality-control-associate-i","title":"OmniaBio: Quality Control Associate I","company":{"id":1099860,"name":"CCRM","domain":"ccrm.ca","url":"https://alion.io/company/ccrm","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Dayforce","truth_index":{"grade":"B","score":75,"open_postings":3,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-11-09T06:03:00Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"junior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Hamilton, Canada"],"countries":["CA"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":40000,"max_usd":66000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":233},"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-09-24T04:00:00Z","employer_posted_date":"2026-10-02","last_verified_at":"2026-11-09T11:05:08Z","board_verified":true,"closed_at":null,"days_open":46,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":46},"description":"Active Vacancy\nPosition Summary: \nAs the Associate I, Quality Control at OmniaBio, you are a motivated individual with a keen interest in the field of quality control (QC) for Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products, driven by the opportunity to enable clinical translation of cell therapy and regenerative medicine. The Associate I, Quality Control, will be required to work across the entire range of activities, including but not limited to, testing, sample management, equipment qualification, method development and optimization, and data review. You will demonstrate flexibility within the Quality team and larger organization, managing work priorities, as required. You will ensure the high-quality delivery of contract services. \n\nResponsibilities: \nDelivers quality control-related services, including sample management, testing, method development, optimization, qualification and validation, stability program, data review and equipment management. \nComplies with all standard operating procedures (SOPs) and work practices. \nMaintains the materials specification program, as directed. \nReleases materials, as directed. \nManages the retain and reference standard program, as directed. \nAdheres to the QC documentation quality management system program, including SOPs, logbook and associated forms. \nMaintains the sample management program, including sample identification, storage and retention. \nPerforms material testing in compliance with approved and current specifications, including but not limited to, incoming materials, in-process materials, drug substance materials, drug product materials, environmental monitoring samples, and stability samples, as required. \nParticipates in internal audits and/or supplier audits, as required. \nParticipates in client audits and health authority audits, as required. \nCollaborates with the Facilities and Engineering team to ensure that facilities are available for production, including but not limited to, room readiness and environmental monitoring data. \nReviews and assesses deviations, corrective and preventative actions, change controls, etc. \nContinuously grows and adapts in a fast-moving field to keep yourself and the organization at the forefront of the cell and gene therapy and regenerative medicine fields. \nEnsures GMP is embedded in all manufacturing related tasks. \nEngages and supports the OmniaBio Operating Model continuous improvement philosophy. \n\nRequirements: \nHigh school diploma, college diploma preferred. \n1-2 years of experience in cell therapy/viral quality control department supporting GMP production, or similar within the pharmaceutical, medical technologies, biologics or similar industries. \nExperience working for a CDMO, a third-party testing facility or a biotechnology company performing similar activities. \nStrong understanding of cell manufacture processes and technologies. \nExcellent understanding of Health Canada/US Food and Drug Administration GMP regulations and quality assurance principles. \n\nDesired Characteristics: \nSound knowledge of applicable regulatory frameworks and requirements for cell and gene therapy and regenerative medicine, such as GMP, ISO, or medical device development. \nIndependent, detail-oriented self-starter with excellent analytical skills and able to multitask and succeed in a team environment. \nExperience establishing customer-facing organizations and service models. \nDemonstrated initiative and the ability to deliver high-quality 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