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We are seeking a highly organized and detail-oriented individual to fill the role of Document Control Specialist. As a key member of our team, you will be responsible for administering and updating project reports, related documentation, and other ad-hoc reports to ensure accurate and timely review and communication of information within and outside the engineering team.
Main Responsibilities:- Support the engineering team by managing and maintaining project documentation, including reports, drawings, and other technical documents.
- Process and manage vendor documents, ensuring compliance with established standards and procedures.
- Perform spend checks on each project to ensure accuracy and completeness.
- Track and provide metrics to management on the status of project-related documents.
- Maintain confidentiality around sensitive documentation.
- Minimum 5 years of experience working in the pharmaceutical industry or a multi-national environment.
- Proficient in Microsoft Office, especially Excel, Word, and PowerPoint.
- EDMS essential.
- Proven time management skills with the ability to prioritize and remain focused, working independently.
- Ability to manage conflicting responsibilities and anticipate key deadlines and requirements.
- Proven ability to develop effective working relationships.