LSC have a great contract opportunity for a Quality 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:
- Execution of the Quality Risk Management (QRM) & Site Quality Risk Register (SQRR) processes ensuring effective governance, communication and management systems are in place and maintained.
- Execution of the Quality Internal & External Audit/Inspections preparation and management processes for the Site (including follow up on audit action completion, associated CAPA's, and NC Quality approval).
- Participate in Site risk assessments.
- Manages projects effectively to meet strict timelines and achieve established milestones with regular updates to Quality and Site Leadership Teams.
- Quality Review and Approval of SOPs, Work Instructions and forms from other departments and periodic reviews.
- Quality review and approval of quality non-conformance (NC) records. Quality point of contact for attendance at Root Cause Analysis meetings.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Experience with data integrity as a QA Specialist and with risk management projects and driving improvements.
- Third level Degree in a science or pharmaceutical discipline.
- A minimum of 3 to 5 years' experience in a quality or compliance role within the biological and/or pharmaceutical industry
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!
