We are seeking an organized and detail-focused professional to support the management of documentation for medical devices and new product introductions. This role offers a unique opportunity for development, with structured training provided to help you grow into the position and contribute to wider operational and quality assurance functions.
Key Responsibilities:
* Initiate requests for changes to documents
* Routinely manage controlled documents through approval and implementation processes
* Issue, maintain, and archive controlled documentation
* Track and report document control metrics to senior management
* Support operational and QA teams with documentation-related tasks as required
Maintaining compliance with relevant training requirements is also essential in this role.
Evaluation Criteria:
* Strong planning and organizational 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
This position requires self-motivation, teamwork, and independent working skills.
Requirements:
* Minimum 1 year experience in document control environment
* Prior experience in medical device industry is essential
* Proficiency in managing change control requests, document revisions, and working within strict document control protocols