We have an excellent opportunity for a CQV Engineer to join a global Biotech company in a state-of-the-art facility in County Westmeath initially on a 12-month contract basis.
You will be working on a clinical project and reporting into the CQV Lead.
Who are we looking for?
We are looking for an experienced CQV engineer with strong experience in the Biotech / Pharma fields.
Ideally, you will have experience with Upstream, Downstream or single use manufacturing processes
Experience working with Delta V Manufacturing Systems is also a desirable requirement and should be highlighted within your CV.
What will your role involve?
Your duties will include, but not be limited to:
- Responsible for generating CQV test documentation which includes VQAs, VTP, DRRs and test scripts.
- Execute testing and verification in the field on upstream and downstream processing equipment.
- Raise and close validation deviations where required.
- Understanding of risk-based verification approach for clean utilities, black utilities, downstream and upstream processes.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta Consultancy Services does not sponsor Visa applications.
Republic of Ireland
A global biotech company requires a CSV Engineer to join a new project in central Ireland. The CSV engineer will be responsible for the development of key AIT quality documents, such as Quality
Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing manufacturing facilities all over the country. An exciting opportunity
Fancy a change from busy city life? Why not consider working for a global Biotechnology organisation in the picturesque Munster region of Ireland! An international airport just 30 minutes from
Send us your CV
Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.