Description
An exciting opportunity has arisen for a Validation Technologist to join a successful and growing Pharmaceutical team in the South East. You will be involved at all stages of the validation life cycle including specification of new items, through to testing and documentation to ensure that the systems are fit for purpose and compliant with regulatory requirements for the duration of the system's life.The organization are very pro-active with employee career development and there are endless opportunities to expand your skill set in the future, within the Quality team should you wish.
Salary: Up to £33,000 plus benefits
Main responsibilities will be to:
- Minimize business risk associated with the processing and storage of electronic documentation ensuring continuity over the equipment and product's life cycle.
- Write, review and approve validation documentation including protocols and reports and manage the timely closure of any discrepancies or non-conformities.
- Providing a reliable service to our internal customers to ensure that timescales are met and work is carried out to meet expectations.
- Maintaining the ongoing compliant status of computer systems associated with equipment, facilities and utilities by involvement of the scheduling of activities.
- Communicating validation activities with our internal and external customers and working with them to resolve problems and conflicts.
- In line with overall responsibilities, perform additional tasks assigned by the line manager.
This role is a hands-on position and requires the post holder to be able balance multiple project based activities, coordinating the generation, review and execution of validation protocols with the relevant stake-holders.
I am looking for an individual who has previous experience working in a Pharmaceutical cGxP environment (GMP, GCP, GDP, GLP) involved in validation activities of equipment, utilities and facility clean rooms.
The ideal candidate should also have experience in coordinating qualification activities in both a laboratory and manufacturing environment working with internal customers to deliver compliant systems to within agreed time scales.
Experience of validation life cycle documentation in terms of design, writing, review and execution is a key element to this position.
To apply for this role please email your CV