We are currently seeking a highly organised and detail-oriented Document Control Specialist to support documentation management for medical devices and new product transfers. This is an exciting development opportunity where you will receive structured training to grow into the role and support wider operations and quality assurance functions. This is a 6 month contract opportunity based onsite the facility in Tullamore, Co.Offaly.
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
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
For a confidential discussion about this opportunity, please contact David Smith.
david.smith@collinsmcnicholas.ie
(090) 6450660