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Document Control Specialist
2 weeks ago
This is an exciting development opportunity for a highly organised and detail-oriented professional to support documentation management for medical devices and new product introductions.
Key Responsibilities:
- Initiate change requests for new and updated documents
- Route controlled documents through the approval and implementation process
- Issue, maintain, and archive controlled documentation
- Track and report on document control metrics to senior management
- Support operational and QA teams with documentation-related tasks as required
- Maintain compliance with training requirements for your role
- Perform additional duties as assigned by the quality assurance manager
Essential Skills and Qualifications:
- Strong planning and organisational skills
- Effective interpersonal and communication abilities
- Ability to guide end users on document control processes
- Demonstrated success in supporting documentation for new product launches
- Familiarity with the document control process and ability to support training coordination
- Self-starter with strong teamwork and independent working skills
Experience Requirements:
- Minimum of 1 year's experience in a document control environment
- Prior experience in the medical device industry is essential
- Proficiency in managing change control requests, document revisions, and working within strict document control protocols
Becoming a Document Management Coordinator will provide you with the opportunity to work with a talented team to develop and implement effective documentation strategies.
As a Document Management Coordinator, you will play a critical role in ensuring that our organisation maintains compliance with regulatory requirements and industry standards.
If you are a motivated and detail-oriented individual who is passionate about documentation management, we encourage you to apply for this exciting opportunity.