Qualified Person - Pharmaceuticals

A multinational pharmaceutical manufacturing company are currently recruiting for a QP eligible to release product in accordance with article 51 of 2001/83/EC and Annex 16 of Good Manufacturing Practice Part I (Eudralex volume 4) to work at their flagship site in East Yorkshire

As a QP you will be a key member of the batch release team, ensuring GMP compliance throughout the site and leading QMS maintenance and improvement activities.

Responsibilities

• To undertake routine product certification as a Qualified Person for solid oral, none-sterile and sterile liquids, dry powder sachet dosage forms
• Lead the maintenance of GMP standards across all site operations, identifying areas for improvement and leading quality improvement projects
• Lead, mentor, train and coach the 100+ headcount Quality Department

Requirements

• Registered EU/UK Qualified Person with relevant experience within the pharmaceutical industry
• Good understanding of the pharmaceutical manufacturing sector in the UK and EU countries
• Experience of working with electronic QMS solutions, such as Q-Pulse

Interviews for this QP vacancy are imminent so please apply now or contact Gareth Gooley at Science solutions for more information.