Are you looking for a challenging and rewarding career opportunity in document management? We are currently seeking an experienced Document Control Specialist to join our team and support the development of medical devices.
This is an exciting opportunity to work in a dynamic and fast-paced environment, where you will be responsible for managing documentation related to new product introductions. As a Document Control Specialist, you will play a key role in ensuring that all documentation is accurate, up-to-date, and compliant with regulatory requirements.
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 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 QA Supervisor
Requirements:
* 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 introductions
* Familiarity with the ICDH process and ability to support training coordination
* Self-starter with strong teamwork and independent working skills
Essential 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