Quality Assurance Officer

Google Chrome Microsoft Edge Apple Safari Mozilla Firefox Quality Assurance OfficerFull-timeCompany 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.In over 35 years, Eurofins has grown from one laboratory in Nantes, France to ca. 65,000 staff across a decentralised and entrepreneurial network of 950 laboratories in 59 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 6.9 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionPlan, execute and report audits according to the audit timetable and applicable procedures for the organization, subcontractors, suppliers, and other Eurofins Central Laboratory contacts.Plan and execute protocol, laboratory and supporting data, and final report (interim, draft, final) audits and conduct in-life phase inspections as required for compliance with internal SOPs and bioanalytical method validation guidelines (FDA, EMA).Perform review of raw data against the draft reports of bioanalytical studies to verify that the reports accurately and completely reflect the raw data generated.Perform in life and operational spot inspections- generation of associated reports.Monitor the progress, appropriateness and correct implementation of corrective measures.Prepare, review and improve QA procedures.Review procedures of other departments within the organization.Provide quality-enhance training on your own initiative, annual compliance training, and on request.Act as a contact person for quality questions from the organizationAudit preparation, hosting of client audits and/or regulatory inspectionsReview and evaluate adequacy of investigations and CAPA (corrective actions/preventive actions) reports.Maintain current knowledge of standard requirements according to GCLP, GCP, GMP, CAP, ISO17025 and ISO 15189 guidelines related to the business process.Archive and document control duties as assigned by QA Manager.Perform other related tasks that match training and experience on request of the QA Manager.QualificationsBachelor degree in Life Science or a Quality oriented education ORMLO education with HLO work and think levelAt least 2 years’ relevant work experienceExperience with or strong affinity with quality systems set up according to GCLP and/or GCPWork experience in the field of ISO / IEC 17025 and 15189Confident to engage in the discussion with the managementExcellent command of English, spoken and writtenAble to increase the quality consciousness of employeesStrong analytical skillsResult oriented, sets him/herself concrete targets and does everything to achieve them, considering the common interestContinuously focused on improvement and...