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The company

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.

 

The role

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.

 

Responsibilities

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.

 

Requirements

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

 

Other information

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.