Our client is a great multinational biopharmaceutical company. Their main goal is to create and innovate forms of improving people’s lives with high-quality biopharma products.
As a Quality Assurance Associate you will be responsible for the validation of the equipment used to ensure that medicines are correctly labeled, packaged, and distributed throughout Europe; and responsible for the automation and information systems for the Quality Risk Management Team.
Ensure the equipment is working correctly
Review and approve validation documentation
Manage ABR’s device responsibilities and ensure alignment with GMP regulations
Perform final review of technical change control.
MBO or Bachelor’s degree in Life Sciences or process technology
3 years of experience in the pharmaceutical or medical device industry
Experience with GMP
Fluent in the English language
Are you interested and do you want to apply for this role, please fill out your application via the apply button below and contact Camila Castro.