Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
1. To undertake the samplingactivities of API, Raw Material.
2. To carry out the inspection of incoming packaging components, Incoming Drug suppliesand the inspection of incoming Part Finished/Finished Products within agreed timelines.
3. Approval, Hold or rejection of items on the SAGE system asappropriate basedupon results of inspection or assigned actions through the Achiever system. Liaise withQC InspectorTeam Leader/ members of the QA department for disposition of materials thatdon’tmatch approved material specification.
4. Post holder liaison with relevant Project Managers,supervisorsor managers.
5. Tocomply withcompany policies including internal and external Health and Safety and Environmental standards asrequired.
6. Toidentifyself-development needs for future performance.
7. To liaise with QA to ensure compliance with GMP procedures
8. To ensure training file is up to date with current information and ensure SOP compliance.
9. General housekeeping within the department and compliance with continuous improvement activities.
10. To undertake such tasks and to manage specific internal or ad hoc projects as and whenrequiredto meet department and business needs and within the scope of the job-holder’s capabilities and responsibilities.
11. Minimum 5 GCSE’s (C or above) or specifically quality assurance qualifications.
Knowledge of statistics and their application is desirable but not essential.
Join us and be part of building the bridge between life changing therapies and patients.