|Job title :||Qualified Person (QP)|
|Job type :||Permanent|
|Salary :||£75000 - £80000 per annum + excellent benefits|
|Contact name :||John Spring|
|Contact email :||firstname.lastname@example.org|
This is a permanent role looking for an experienced QP with eligibility to release batches in the UK. The position is part of a team of several QPs with a wealth of experience across pharma, biologics and ATMP products. In this role you will be responsible for improving all activity that relates to QP certification and the release of batches.
Salary & Benefits:
£80k + benefits.
Role and responsibilities:
*Manage compliance issues through the on-site Quality Management System
*Oversee QMS documentation such as CAPAs and deviations
*Act as the subject matter expert for all GMP and QA Operations processes
*Manage the continuous improvement initiatives across the GMP facility
*Mentor and train personnel on GMP guidelines and operations
*Support audits (customer and regulatory bodies)
*Work alongside the Principle QP and other QPs for the release of batches of IMPs and commercial products
Requires skills and qualifications:
*Extensive experience working as a QP on a manufacturing licence (ideally in biologics)
*Excellent working knowledge of QA, QMS and GMP guidelines
*Strong experience of working with MHRA and FDA regulations
*Ability to work individually and as part of a team, hitting project deadlines and targets
*Auditing background - dealing with internal and external audits
This is a great opportunity to join one of the fastest growing global companies in the industry. The role will suit an aspiring QP looking to grow their skill set across some of the most exciting medicinal fields on the market.
To apply for this position and put yourself under immediate consideration, send your CV to email@example.com or call +44 (0) 207 255 6650