Quality Assurance Professional (12mth FTC)

Are you a proactive team player with fantastic  problem solving skills looking for your next step into Quality Assurance? Apply Today! This is an amazing opportunity for a quality professional to gain further industry experience with the potential for QP development!

Shape the LEO Pharma of tomorrow

At LEO Pharma, our mission transcends the conventional. We're on an ambitious path to become the leaders in medical dermatology worldwide. This is a unique opportunity to join the Quality Assurance team at our Dublin Manufacturing site.

In Quality Assurance we share a “challenge accepted” mindset and are guided by our winning behaviours of simplification, collaboration, and accountability, to achieve our goals

Your new role

As a Quality Assurance professional you will have overall responsibility for the batch documentation review process and working closely with the QP’s to ensure alignment on process / product investigations and follow up with corrective actions. Your responsibilities will include, but not be limited to the following:

• Deliver efficient and timely review of Finished Product batch documentation for release and rejection activities.
• Approve batch documentation 
• Approve the decision making on daily queries online and play an active role in the resolution of these issues.
• Perform process confirmations on the production lines with regards to batch documentation and manufacturing.
• Approve process/product investigations (deviations) and follow up corrective actions identified.
• Approve temporary change requests.
• Support Customer complaint investigations and response where applicable.
• Provide Quality inspections system support including action close-outs.
• Update SOP/WI’s as required for the Quality Release Department.
• Complete approval of Quality Management System records, CAPA’s, actions etc
• Ensure completion of read and understand or awareness of relevant documents.
• Participate in training of new personnel and develop training material
• Lead Lean initiatives and in the implementation of latest Quality legislation and guidance developments from Regulatory Authorities and Industry best practice.
• Ensure audit readiness
• Participate in inspections by third parties, e.g. HPRA, FDA, customers, etc.,

This role is based at our Dublin Site full time and is a mix of being on the production line and checking documentation in the office. On site start times vary between 7 and 8am. This role also offers an early finish time on a Friday.

Your qualifications

To succeed in this role, we imagine that you have the following qualifications: 

• Mpharm/ Pharmacist background preferred or Bachelor’s degree in Science or similar 
• Experience in quality within the pharmaceutical industry is preferable
• Strong understanding of pharmaceutical quality processes and systems, manufacturing processes and other support/control systems is desirable.

LEO Pharma is built on collaboration, innovation and curiosity. Is this you? Can you bring this and a proactive hands-on approach with excellent interpersonal and communication skills to this role? 

Your new team

You will be part of the Dublin Quality Team and work alongside 7 experienced Quality Assurance professionals. 

Your application

You do not need to upload a cover letter, but feel free to add a few sentences in your resume or CV on why this position has your interest.