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Merck KGaA
An excellent opportunity has become available for a dynamic IT Compliance Expert responsible for supporting global governance and compliance frameworks in Enabling Function IT. The candidate will be acting as Site Lead User for the electronic Document Management System (currently ManGo based on CARA) for IT globally. In this role, you will provide training, consultation, and guidance to IT personnel responsible for developing and controlling documentation. A key aspect of this position is the ability to work professionally and independently to enforce compliance across different departments and organizational units while supporting users in developing and controlling documents in a timely manner. Additional back-up activities in other Governance areas such as Training Management will also be expected. This position may be located in Bratislava, Slovakia; or Bangalore, India. Who you are:You have a Bachelor degree in Business Administration, Information Technology, or Science (relevant professional experience may be taken into consideration).You have a minimum of 3 years’ experience in controlled document management for a pharmaceutical company. You have expert knowledge of and practical experience applying Good Documentation Practices.You have demonstrated experience as a lead user (operational expert) for validated electronic Document Management Systems.You have a strong quality mindset, attention to detail, and understanding of quality oversight.You have native-level English proficiency and excellent, confident presentation skills.You are a creative and independent thinker, able to balance priorities and organize to meet timelines.
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Merck KGaA
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Merck KGaA
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Merck KGaA
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Merck KGaA
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Merck KGaA
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Merck KGaA
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Merck KGaA
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Merck KGaA
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