|Contact Name:||John Reid|
Due to continued expansion of their operations our client a well-established Multinational Healthcare Manufacturer now require a qualified and experienced QA Documentation Controller.
This is a permanent role based in The Midlands
Key Responsibilities of QA Documentation Controller
Documentation management, including processing, distribution and filing of all documents associated with medical devices using the clients Document Management System
Initiation of change requests for new and amended documents.
Routing of controlled documents through the approval and implementation process.
Issue and maintenance of controlled documentation.
Report to Management on document Control metrics as required
Carry out other tasks or responsibilities as directed by the QA manager.
Requirements of the QA Documentation Controller
Minimum of 2 years' experience working within a QA function in an FDA or ISO 13485 regulated Industry.
Demonstrated understanding of criticality of attention to detail, data accuracy and document control
Must have the ability to communicate effectively with management and fellow peers
Please send an up to date CV and cover letter to John Reid at The RFT Group / firstname.lastname@example.org / on 01-2302400 / www.rftgroup.ie
Follow us on Twitter, Facebook and LinkedIn
The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors.