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 021 4777329 if you have any more questions about this role!
