Your new company

Your new role

• Batch Record Review and material release (including CoA) to ensure compliance with GMP requirements.
• Quality review and approval of Master Batch Record (MBR) record for routine cleaning and process activities, including Automation recipe updates.
• QA Review and Approval of SOPs, Work Instructions and forms from other departments.
• Attendance at Daily/Weekly Operations led Team Meetings.
• Responsible for Gemba Walkdowns & Inspection Readiness Walkdowns from a QA perspective.

What you'll need to succeed

• Third level Degree in a science or pharmaceutical discipline.
• A minimum of 3 years of experience within the Pharmaceutical Industry.
• A working knowledge of quality processes and systems is desirable.
• Demonstrated knowledge and application of industry regulations including those of FDA, HPRA, EMEA and other authorities.

What you'll get in return
Flexible working options available.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
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