Specialist OQA GMP Compliance & Master Records Mainz, Germany | full time | Job ID:8062 As a Specialist QA GMP Compliance & Master Records, you will ensure that master records, validation protocols, etc. are well documented, reviewed and approved by QA. In addition, this position supports general GMP compliance at the site. Contribute that controlled documents are well documented, reviewed and approved by QA, with includes batch records of diverse projects and manufacturing steps Support the design and review of master records and templates used for the review and release of GMP products Ensure GMP compliance of the batch record review process as well as related processes to this topic Initiating, implementing and monitoring change controls, deviations and CAPAs Follow-up with Key Quality Metrices (KPIs) as required Apprenticeship with a scientific background or university degree (pharmacy, biology, chemistry, or a similar discipline) Professional experience in the pharmaceutical industry (e.g. in quality assurance, pharmaceutical production, quality control) and within the GMP environment Deep expertise and practical experience within Operational Quality Assurance Profound knowledge of relevant US & EU regulations, EMA, FDA and other regulatory standards as well as Good Manufacturing Practice High team spirit, excellent collaborating skills, and effective stakeholder management skills High carefulness and accuracy in the way of working, conscientiousness and detail-orientation Great communication skills and fluency in English and German Your flexibility: flexible hours | vacation account Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential Your health and lifestyle: Company bike Your mobility: Job ticket | Deutschlandticket Your life phases: Employer-funded pension | Childcare