LSC have a great contract opportunity for QA Specialist to join a Cork based biopharma company.
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Batch Record Review & material release to ensure compliance with GMP requirements.
- Review & Approval of Event, Deviations, and Customer complaints.
- Supports all validation activities on site as described in the Site Validation Master Plan
- Carries out tasks related to the administration of site supplier approval process.
- Co-ordinates and assists in the preparation for regulatory and customer GMP inspections of the site
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Experience as Quality Assurance Specialist in QA Operations, 3-5 experience in a quality, validation or compliance role within the biological and/or pharmaceutical industry.
- Bachelor's degree in a scientific/technical discipline required
- Experience in auditing of external suppliers, contractors, and vendors
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 Grainne Hodnett at +353 214771329 if you have any more questions about this opportunity!
