Document control specialists play a pivotal role in ensuring the smooth operation of 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 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.
Essential Criteria:
* Strong planning and organisational skills
* Effective interpersonal and communication abilities
* Able 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
Successful candidates will possess a minimum of 1 year's experience in a document control environment. Prior experience in the medical device industry is essential.