Description
Our client, a pharmaceutical company, is looking for an experienced Qualification/Validation Engineer to support them on a new transfer project.The Qualification/Validation Engineer will be responsible for leading OSD equipment packages given to them.
Location: Dublin region, Ireland
Contract Duration: Until end of 2015
Start Date: As soon as possible
Tasks:
- Write Test Scripts for Qualification/Validation - Create VQS (Verification Quality Strategy).
- Execute the Test Scripts.
- Complete Testing of equipment.
- Handover to operations.
- Proven Engineering experience.
- Strong experience working on pharmaceutical projects.
- Oral Solid Dosage experience is essential for this position as well as experience working with the OSD equipment listed below.
- Experience of completing full life cycle Qualification and Validation projects (Equipment IQ/OQ/PQ).
- Previous experience of writing Test Scripts.
- Excellent knowledge of GMP regulations.
- High Containment Tablet Pressers/Tablet Coater
- Granulation
- Milling
- Blending
- Active Isolator
- IPT Washer