A Biotechnology company based in the Republic of Ireland are recruiting a QA Validation Specialist to provide validation, qualification technical support and oversight for the manufacture of their medicinal products.
Responsibilities for the role:-
- You will prepare and maintain the site validation plan and be responsible for the archiving of validation/qualification documentation
- You will interact with other departments for example Engineering, Laboratories, Operations, Warehouse and Process Development to ensure that site validation plans are understood and keeping in line with site objectives
- You will support the generation of process and QC equipment installation and operational performance qualification, review and approve the qualification protocols, discrepancies and reports for quality
- You will maintain understanding of cGMP, Good Engineering Practice and guidance in relation to all aspects of validation across manufacturing, laboratories and facilities.
The client are wanting to hold interviews for this role immediately so please apply or call Natalie for further information.
