Reference Number: JO-2107-473425
Validation and Qualification Scientist
Job Type: Contract
Our Client have an exciting career opportunity available for a Validation and Qualification Engineer based at the site in Reading.
In this role you will be a key part of the team responsible for monitoring equipment/facility and Qualification/validation and calibration/maintenance of all GMP equipment.
Duration: 3 months
Rate: 200ppd to 250ppd
Other main tasks and responsibilities include but are not limited to:
Lead validation/qualification projects and complete all associated documentation in line with regulatory expectations
Manage, coordinate and guide the execution of the site validation master plan
Provide the relevant support for regulatory audits, submissions and other auditor requests
Develop and write commissioning, qualification and validation documents following established standards and templates.
Execute test protocols
Ensure that equipment/facilities are managed in conjunction with all regulatory requirements such as health & safety, cGMP, construction, environmental, etc.
Ensure Data Integrity compliance is maintained in the qualification/validation of equipment and systems
Perform and conduct P&ID walk-downs and verification of system drawings
Ensure the qualification/validation status of equipment and systems are in compliance with cGMPs at all times.
Manage validation documentation, commissioning test scripts, qualification validation protocols, summary reports and risk assessments
The successful candidate will be educated to a minimum A level and having minimum 5 years Validation/qualification experience in a regulated environment.
Experience in Pharmaceutical industry will be preferable. Have excellent written and verbal communication skills and be proficient in Microsoft Office Word, Excel, PowerPoint etc.
Applicants must have the right to work in the UK upon being offered employment.
To apply please send your CV to Nick Buck email@example.com