This is your chance to work for a company that is a pioneer in gene and cell therapy focussing on long-term curative treatments. With vast investment being made into the organisation and new build projects on the horizon, this is the ideal time to join the team and establish yourself as a key team member. They are led by an experienced executive team that is leading them to a bright and exciting future.
In this role, you will be supporting the validation of equipment, facilities, utilities and processes in accordance with GMP requirements. You will be preparing and maintaining validation plans, assisting systems owners with impact assessments and identifying validation requirements as well as the execution of validation protocols (equipment, facilities, utilities, computerised systems and processes).
You will have the following experience/qualifications:
- Working knowledge of biopharmaceutical or pharmaceutical industry regulations and guidelines that relate to qualification/validation
- Demonstrable experience of validating manufacturing/laboratory equipment, facilities/utilities and processes
- Generation/execution of lifecycle documents (URS, DQ, IQ, OQ and PQ) in a biopharma, pharma or related industry
If this role is of interest, apply directly now or get in touch to find out more information!
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.
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