JOB VACANCY: Validation Lead
We are looking for a GMP experienced validation/qualification professional to progress their career with us in the exciting area of cell & gene therapies. With 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. As Validation Lead you will work across GMP manufacturing, Quality Control laboratory facilities and the Cryostorage facility to ensure that all aspects of validation comply with relevant regulations.
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). This will include cleanrooms, medical gas supply and computer systems including environmental monitoring-systems.
You will have the following experience/qualifications:
A Degree (or equivalent) in a Science or related discipline
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
Experience of computer validation systems is desirable.
We offer excellent opportunities for career progression along with training and the chance to be a part of a growing organisation. We also offer an attractive base salary and benefits package.
The candidate must have the right to work in the UK.
Interested candidates are encouraged to submit a CV and a supporting letter to email@example.com