This is a permanent, full – time position working Monday to Friday with flexibility on starting and finish times. There is currently a mixed pattern working from home and in the office, though this role will ultimately be based on site to allow smoother workflow. There is a competitive salary plus benefits, which will be discussed on application.
The Role
Based in a team of 7, you will be responsible for managing the validation aspects of projects including scheduling work, agree timeline and liaise with other departments. You will schedule and ensure computer systems (ERP system) is validated and qualified for its intended use and own part of the requalification schedule. You will generate validation documents prior to executing according to SOP’s and execute test protocols according to set timelines.
You will provide validation support and input to projects and site-specific meetings as required and mentor junior members of the team. Working in a fast-paced, highly process-driven sterile manufacturing environment, you will encounter a range of technical challenges and opportunities to collaborate with scientific, engineering, quality, and production teams.
Benefits
- 25 days' holiday
- Stakeholder pension plan
- Life insurance, long term disability and BUPA medical plan schemes
- Discretionary, non-contractual annual bonus
- Commutable by car with free parking, and within walking distance of train station / bus routes
- Childcare voucher scheme
Experience
The successful candidate will be a conscientious, attentive individual with experience in GMP in a role validating computer systems (ERP system or other systems) according to GAMP 5, QC, QA, Production, Engineering, or IT Testing, ideally from the pharmaceutical industry. You will ideally have a degree (or similar) in a scientific or engineering discipline. You must have a good understanding of manufacturing processes, laboratory equipment and computer systems. You must be able to demonstrate reviewing documents and data, writing quality reports as well as ensuring the meticulous checking and qualification of equipment or computer systems. You will need excellent communication and team working skills, with the ability to handle your own workload, organize your own time and follow Standard Operating Procedures (SOPs).