Eurofins 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 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years. The role involves leading investigations related to Out of Specification (OOS) results, deviations, and Corrective and Preventive Actions (CAPA) within a cannabis testing laboratory. The candidate will ensure adherence to Standard Operating Procedures (SOPs) and regulatory guidelines while conducting daily OOS investigations. Responsibilities Include: + OOS Investigations: Lead OOS investigations, documenting findings with input from Subject Matter Experts (SMEs), managers, and Quality Assurance (QA). Review all associated raw data and records, determine the sequence of events, and conduct root cause analysis. Develop hypothesis testing plans collaboratively with QA and clients, providing systematic and detailed OOS reports. Work with operations and QA to decide on corrective/preventive action plans for OOS results. + CAPA Process: Participate in or champion the CAPA process, investigating CAPAs on behalf of Quality Control (QC) and reviewing them according to CAPA SOPs. Ensure timely completion of investigations as per SOP. + Validation and Audits: Conduct validation or failure investigations as needed. Follow up on corrective actions from internal and external audits, supporting the preparation of responses to external audit reports. + Client Interaction: Address client requests and complaints effectively, ensuring timely communication regarding any issues that may impact deadlines. + Deviations Management: Initiate, lead, and investigate deviations, performing root cause analysis and corrective actions in accordance with internal SOPs and regulations. + Documentation: Write stability protocols as per client requests, review QC methods, validation protocols, or reports of methods or equipment. Perform reviews of calibration records or testing records and conduct impact assessments as necessary. + Training & Compliance: Train departmental staff on documentation practices, regulatory issues, and corrective actions. Maintain a clean and organized working environment according to laboratory procedures. + Reporting: Prepare weekly progress reports on assignments and ensure that all training records are current. + Minimum of a Bachelor’s degree in Biology, Biochemistry, or a related field; + Over 5 years of experience in pharmaceutical or cannabis testing with exposure to root cause investigations and quality management systems. + Knowledge of OOS investigation regulatory processes is essential. + LIMS and transfer program experience considered an asset + GMP and ISO17025 testing experience is required (3 to 5 years) Skills: + Proficient in using root cause analysis tools. + Strong understanding of scientific principles relevant to the investigations. + Ability to work under pressure with tight deadlines while managing multiple assignments. + Excellent written and verbal communication skills. + Self-starter, ambitious and energetic + Proficiency in standard office software (Word, Excel, PowerPoint, Outlook). + Candidates must maintain a proactive attitude towards training and compliance with SOPs while demonstrating attention to detail in all duties performed. Working Conditions: This position is based in a laboratory environment; significant time spent standing at a bench, working with chemicals and biologicals, and in a time-sensitive production role. Lifting requirements of up to 30lbs on a regular basis. Extra hours, weekends and evenings will be required.  Candidates currently living within a commutable distance of the GTA are encouraged to apply. 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.ca We 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. NO AGENCIES, CALLS OR EMAILS PLEASE