We have created a position for a Quality Management System Manager, based in London (UK) or Madrid (Spain). The following are the key responsibilities for this role:

• Implement company Quality Management System
• Support product development, manufacture and market authorisation
• Contribute with documentation for Common Technical Document for submission for marketing approval of Stablepharma reformulated vaccines.

Requirements:

• A Bachelor degree in Life Sciences (BSc), preferably pharmacy.
• At least 5 years’ experience in quality environments within the pharmaceutical sector.
• Good understanding of the overall medicines development process. • Experience in development and regulatory is an advantage.
• Fluency in written and spoken English.
• Good organisation & time management skills
• Positive attitude and flexible approach to work

Please send your CV to [email protected]