LSC have a great contract opportunity for a QA Specialist to join a pharmaceutical company in Cork.
If you have 3 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you
ABOUT THE PROJECT - KEY RESPONSIBILITIES: 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.
QA review and approval of Warehouse Shipping Picklist.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
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.
Note: Are you currently eligible to work in Ireland?
As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply
Apply via this advert or contact Cian Marnane at LSC on if you have any more questions about this role
Skills: Qualiy Assurance Quality Systems Documentation Control Batch records