Company Description

Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, 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 for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing.

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.

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 generatedMonitor the progress, appropriateness and correct implementation of corrective measuresPrepare, review and improve QA proceduresReview and approve procedures of other departments within the organizationProvide quality-enhance training on your own initiative and on requestAct as a contact person for quality questions from the organizationAssist with the preparation and 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 processArchive and document control duties as assigned by QA ManagerPerform 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, taking into account the common interestContinuously focused on improvement and optimization of technology and the work processOrganizational talent, continue to perform effectively under pressure and know how to monitor progress

Additional Information

What we offer: As an employer, we’re keen to look after our people with as much dedication as they look after our patients. That’s why we offer competitive salaries, excellent training and exceptional career prospects. We’re a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career.

Your data: 
As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.

Eurofins Mechem is an Equal Opportunities Company.