Our client is a professional Biotechnology and Pharmaceutical organization, based in Hamburg Germany.
Our client is offering a great role in the city of Hamburg. They offer a great and very complete compensation package and are known for being a great employer in Germany.
Ensure that the QM documentation and the IT systems are in compliance with the legal requirements and also meet the requirements of Global QA.
Coordinate project-specific regional QM teams in the Europe Central North region. Perform self-inspections. Participate in external QA forums and continue to form. Plan and carry out quality management training courses. Ensure that the legal requirements for training are adhered to. Advise the organization on quality management issues. Create standard operating procedures (SOPs) and check existing SOPs. Check documents for compliance with legal / normative requirements. Check the effectiveness of corrective / preventive measures and changes.
Completed a science degree, ideally in the field of pharmacy or completed science degree with experience in pharmaceutical activities Experience in the validation of IT systems Experience in highly regulated environments Experience working in interdisciplinary project teams Fluency in English
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