The main purpose of the role is to support manufacturing areas with QA support including but not limited to the following:

• Real time in situ batch documentation review
• Real time assessment of manufacturing events from a QA perspective.
• Provide clearance to precede instructions in manufacturing following unplanned events.

Requirements

• The successful applicant will hold a third level degree incorporating Quality Assurance / Management and will have at least two years' relevant experience in Pharma / GMP related role.
• Experience with desktop and internet-based software applications (e.g. electronic document management system, MRP System) an advantage but not essential.