Key skills
CommunicationCritical ThinkingNegotiation
About this role
Role Overview
- Provide global oversight for the development and maintenance of global QMS documents
- Ensure consistent execution of the Global QMS document management process
- Manage the QMS document process, ensuring adherence to the overall process, architecture, and defined timelines
- Provide technical editing support to ensure writing standards are followed
- Maintain effective working relationships with local and global colleagues
- Continually improve the QMS process and associated tools/templates
- Drive and contribute to continuous improvement and lifecycle management of quality system documents
- Communicate QMS document information to appropriate stakeholders and ensure intersections and touchpoints with other teams
Requirements
- An academic degree or equivalent
- At least 5 years of experience in the pharmaceutical industry
- Extensive knowledge of pharmaceutical quality systems, standards, and global Health Authority regulations
- Experience with Quality Systems, document management, and technical writing
- Strong communication and negotiation skills
- Ability to work across multiple departments/sites and in cross-functional teams
- Critical thinking skills to make sound decisions and determine pragmatic solutions.
Benefits
- Relocation benefits not available for this role