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About the role

Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionThe Calibration & Metrology Specialist is responsible for ensuring the compliance, reliability, and performance of laboratory instrumentation and associated software systems within a GMP-regulated environment. This role supports calibration, qualification, preventative maintenance, and data integrity activities across Chemistry and Microbiology laboratories.Depending on experience level, the role may range from hands-on execution of calibration activities (Junior) to leadership of the calibration function, including planning, oversight, and strategic metrology operations (Senior).Core Responsibilities:Perform calibration procedures on laboratory instruments and equipment in accordance with established protocols, industry standards, and regulatory requirements (FDA, Health Canada, ISO/IEC 17025), including HPLCs/UPLCs, GCs, Karl Fischer (KF) titrators, UV spectrophotometers, dissolution apparatus, wet chemistry analyzers, stability chambers, incubators, TOC analyzers, and related instrumentationConduct metrology assessments using precision instruments to verify equipment accuracy and functionalityDevelop, implement, and update calibration procedures, work instructions, and schedules to enhance efficiency and maintain quality standardsMaintain detailed calibration records, documentation, and traceability reports to ensure regulatory compliancePrepare, write, review, and execute qualification protocols (IQ/OQ/PQ) for new and modified laboratory equipmentTroubleshoot equipment malfunctions, coordinate repairs with external vendors, and ensure instruments remain in GMP-compliant, validated, and operational conditionAnalyze calibration data and generate reports to identify trends, deviations, and areas for improvementPerform data integrity assessments for laboratory software and systems to ensure compliance with cGMP and ICH guidelinesDevelop, review, and maintain QA-controlled documentation related to calibration, qualification, and maintenance, including Validation Master Plans and equipment inventoriesRespond to instrument alarms and system monitoring alerts, including off-hours support when requiredConduct temperature/humidity excursion investigations and prepare deviation reportsOperate and manage laboratory information management systems (LIMS) for calibration tracking and documentationCollaborate with laboratory teams, QA, and Metrology/Engineering leadership to schedule calibration activities and minimize operational disruptionsTrain laboratory personnel on equipment use, techniques, and compliance requirements; maintain training records and support competency developmentSupport audit readiness and participate in internal/external audits; prepare responses to audit findings and regulatory inspectionsLead or support change control processes for new or modified equipmentSenior-Level Responsibilities (in addition to above):Lead and coordinate calibration/Metrology team activities, work schedules, and workload prioritization while maintaining hands-on involvement in complex calibration and troubleshooting activitiesDevelop strategic calibration and metrology planning initiatives, including equipment lifecycle management, preventative maintenance optimization, and resource allocation across laboratory platformsProvide advanced troubleshooting expertise and technical guidance on complex instrument issues, failure analysis, and resolution strategiesMentor junior staff and provide technical guidance on calibration best practices and skilled troubleshooting methodologiesManage instrument budgets and lifecycle planningConduct performance reviews for direct reportsDrive continuous improvement initiatives within metrology systems and processes, including procedure enhancements and efficiency optimizationQualificationsEducation & ExperienceBachelor’s degree in Science, Engineering, or related field2+ years (Junior–Mid) OR 5+ years (Senior) in calibration/metrology/validation rolesExperience in a GMP-regulated pharmaceutical or laboratory environment (3–10+ years depending on level)Experience in pharmaceutical testing or regulated laboratory operationsTechnical KnowledgeStrong understanding of GMP, cGMP, and ICH guidelinesHands-on experience with laboratory instrumentation calibration and qualificationFamiliarity with validation lifecycle (IQ/OQ/PQ)Understanding of laboratory software systems and data integrity principlesExperience supporting audits and regulatory inspectionsCore CompetenciesStrong troubleshooting and analytical problem-solving skillsAbility to work independently and within cross-functional teamsExcellent communication skills (written and verbal)Strong organizational and time management abilitiesAbility to perform under pressure and manage multiple prioritiesProactive, detail-oriented, and quality-driven mindsetAdaptability to new technologies and systemsWorking ConditionsLaboratory and office-based environmentOccasional evening/weekend/off-hours support may be required (e.g., system alarms or critical issues)Initial onboarding/training may require on-site presence (e.g., Toronto-based training period)Additional InformationPlease note that relocation to Mississauga, ON is expected in mid-2026.At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.caWe thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.This posting is supported by AI technology to assist in screening candidates and resumes. This posting is for a current vacancy and the successful candidate will start as soon as possible.Disclaimer: Salary information posted on sites other than the official careers page does not reflect the organization’s compensation and may represent estimated ranges provided by third-party job boards. The organization offers competitive wages and a comprehensive total rewards package, which will be discussed during the interview process.NO AGENCIES, CALLS OR EMAILS PLEASE

Compensation: CAD 50000 - CAD 80000 - yearly

About Eurofins

Medical and Diagnostic Laboratories

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