Copy of Clinical Supply Associate – Consultant Assignment at AstraZeneca at WeQuel

Gothenburg, Västra Götaland County, Sweden -

Full Time

Start Date

Immediate

Expiry Date

20 Sep, 26

Salary

0.0

Posted On

22 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Supply Chain Management, Documentation, Product Quality Complaints, Deviation Management, Electronic Trial Master File, GMP Standards, User Acceptance Testing, Visual Management, Problem Solving, Process Standardization

Industry

Business Consulting and Services

Description

Join us in Pharmaceutical Technology and Development (PT&D) where we transform innovative science into actual medicines that help millions of people globally. As a Clinical Supply Associate (CSA), you will support the Clinical Supply Chain Management team in delivering clinical material and associated information to meet agreed clinical demand. This role is perfect for those who thrive in a task-based, agile, and global environment. You will have the opportunity to develop leadership skills and enterprise acumen, becoming a super-user and leading improvement initiatives within a year. This role is a great opportunity for someone pursuing a career within Clinical Supply/Quality Management What you’ll do: The CSA supports Clinical Supply Management with task-based activities that include: Documentation and coordination Product Quality Complaints Coordination of Product Quality Sample Returns. Documentation and facilitation of Deviations affecting product quality or regulatory compliance. Management of documents in the electronic Trial Master File and quality control Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards. User Acceptance Testing Utilising Supply Chain Management systems to support agile ways of working. Continually improving the Clinical Supply Chain processes through visual management, problem solving, global standardisation and process confirmation. AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

Responsibilities

The Clinical Supply Associate supports the delivery of clinical materials and manages documentation related to product quality complaints and deviations. They are also responsible for maintaining the electronic Trial Master File and ensuring inspection readiness according to GMP standards.