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We are currently seeking two committed Quality Assurance specialists to join the AstraZeneca team in Gothenburg.
Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies? We are now looking for 2 Quality Assurance specialists with GMP focus to the Gothenburg team at AstraZeneca!
The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.
Purpose, Offer and Benefits
This is a 1-year consulting assignment starting in June. You will be employed by TNG during the duration of the assignment.
At AstraZeneca, we´re proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
Your Responsibilities
The Bigger Picture
The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. In the role as a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.
Our Expectations
