LSC work exclusively in the Life Science sector; founded and run by contractors we understand contracting first hand and have created a unique solution to make the process as easy as possible - so you can focus on getting your work done!
At LSC we partner with you for the long term, not just your contract duration. We are committed to building relationships and will work with you to ensure you are placed on projects that challenge and reward you throughout your career.
QA Validation Consultant - CSV is required for an innovative and rapidly growing Biopharmaceutical company in Limerick. The new facility is close to completion and is responsible for the production, packaging, labelling and delivery of biopharmaceutical medicines for global markets. The company currently markets medicines for various diseases and has a rich pipeline of products.
The QA Validation Consultant - CSV will be responsible for:
o Generation, execution, review & approval of IOQ protocols and associated validation documents and CSV assessments e.g. Part11 Assessments, etc. related to IT Infrastructure systems and related IT Applications and system components
o Prepares/reviews validation documentation related to projects/change controls.
o Manages change controls and other compliance related tasks e.g. non-conformances.
o Participates in the review of current and future CSV procedures and polices
o Analyzes the results of testing and determines the acceptability of results against predetermined criteria.
The QA Validation Consultant - CSV will have:
o Requires BS/BA in Engineering, Chemistry, or Life Sciences with 5+ years of related experience within the fields of Automation and Computer systems and IT Infrastructure Qualification/validation; will substitute relevant experience for education.
o Experience in a GMP environment essential.
If you would like to hear more about this QA Validation Consultant - CSV role, then please contact Kathy at LSC on 021-4777329 or apply directly through this advert.