Our Biopharma client is looking for a QA Document Controller to join the Quality team on a 12 month contract.
POSITON SUMMARY:
The Quality Assurance Document Control (QADC) specialist is responsible for maintaining and continuous improvement of site quality systems, providing quality oversight of the facility with a focus on document management quality system.
RESPONSIBILITIES:
* Process site-controlled documents on the site Document Control System.
* Approve document change controls and establish document effective dates.
* Complete work according to established priorities and policies to assure product documentation is delivered on schedule.
* Support and train other staff members on the implementation of global improvements related to the Document Control System.
* Train and support other staff members on the use of the Document Control System.
* Maintain the Sites Document Store and escalate any potential issues.
* Control and issue controlled document numbers as required.
* Support Inspection Readiness for the site and the site in preparation for upcoming inspections.
* Examine the Quality Metrics related to the Document Control System.
* Participate and support Continuous Improvement for the Quality Team.
* Other duties may be assigned as requested.
EDUCATION/EXPERIENCE:
* Strong communication and organisational skills required.
* Experience with QMS and EDMS systems is desirable.
* Experience with excel / metrics generation is desirable.