

CPI
Why this role is important for CPI’s
work
As the GMP Document Administrator, you will be responsible for establishing and maintaining the document management processes including the issuing and reconciliation of GMP documentation. You will be joining the established, growing Quality team. Reporting to the Quality Manager – Biologics, you will be working in CPI’s National Manufacturing Biologics Centre and supporting the new, state-of-the-art , also based at the site in Darlington.
You will perform a variety of tasks in support of Document Control Systems’ and ‘Writing, Reviewing, Version Control, Issuing & Archiving of BMR’s and Logbooks to ensure compliance to the CPI Biologics quality management system to meet GMP requirements.
Key tasks will include (but are not limited to) the below:
The person we are seeking
You will be educated to a minimum of 5 GCSE’s (or equivalent) including Mathematics and English Language.
You will have great attention to detail.
It would be great if you had:
What does CPI offer you?
At CPI, we offer a wide range of benefits to our employees, this includes:
To apply for this job please visit uk.whatjobs.com.