Job Description
QA Supervisor, Quality Systems
Our client, is a blue-chip multinational pharmaceutical manufacturer based in Dublin, now seeks a QA Supervisor to ensure manufacturing compliance with their Quality Systems for the site and management for the group.
The successful candidate will focus on document/records management, GMP training and change control system with an emphasis on streamlining, simplifying and providing innovative solutions to existing systems within these areas.
This is a permanent role based in Dublin.
Responsibilities of QA Supervisor, Quality Systems:
Development and maintenance of the Quality Management System
Preparation, update and delivery of GMP training including preparation of course material
Development of site training curricula, training material and SOPs for the site training program
Management of the interface between document control and training
Manage the overall change control system and support the site change control gatekeeper
Completion of performance evaluations and meetings with direct reports
Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements
Authoring, review and approval of Quality related procedures
Support Regulatory Inspections at the site.
Requirements for QA Supervisor, Quality Systems:
BSc in Science or related discipline, MSc would be ideal.
5+ years? experience in a pharmaceutical environment, with proven experience of cGMP guidelines and FDA regulations.
Direct experience of document/records management and systems is required.
Excellent management communication & presentation skills are essential.
Excellent time-management & organisational skills along with a proven ability to multi-task.
Please phone Larry on +353 1-2302400 / larry@rftgroup.ie
The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. www.rftgroup.ie