QA Inspector – Weekend Shift – Galway
This role is a great opportunity for someone with 2+ years’ experience in Quality Assurance / Documentation within a pharmaceutical / manufacturing environment. In this role, you will be tasked with ensuring all products and documentation comply with GMP and regulatory requirements.
Job Details
- Approve incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials.
- Carry out finished goods/end of line inspection prior to product release and shipment.
- Follow through on any corrective actions or deviations raised against particular batches.
- Ensure compliance with current GMP and to assist with training in same.
- Review of standard operation procedures and update where necessary.
- To carry out other duties and undertake other responsibilities as may be assigned by the Quality Manager or his/her designate.
Educational / Professional Details Required
- Previous experience in a pharmaceutical / manufacturing environment.
- 2+ Years experience in Quality Assurance / Documentation
- Preferred Science Qualification.
- Good GMP & GDP Knowledge and experience.
For further information or a confidential discussion please contact Liam Jones
061 363318
liamjones@cregg.ie