Clinical Supply Associate at AstraZeneca

Are you comfortable in a high-paced and agile environment? AstraZeneca in Gothenburg is looking for a Clinical Supply Associate.

Do you aspire to develop leadership skills? AstraZeneca in Gothenburg is seeking a Clinical Supply Associate to join the team, offering an excellent opportunity to work in a task-oriented, agile, and global environment.
Don´t miss the chance - Apply today!

Purpose, Offer and Benefits

This is a one-year consulting assignment starting in February. This means that you will be employed by TNG throughout the duration of this assignment.

At AstraZeneca, we believe in the potential of our people, and you´ll develop beyond what you thought possible! We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

Your Responsibilities

• Timely management of temperature excursion assessment affecting clinical trial material.
• Coordination of the country release requests of study labelled material.
• Electronic document archiving and quality control.
• User Acceptance Testing of digital systems.
• Support the coordination of the purchase and delivery of External Commercial Products.
• Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards.
• Documentation and coordination of product complaints and GMP deviations.
• 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.

The Bigger Picture

In this role you will have the opportunity to develop leadership skills and enterprise acumen, quickly becoming a Super User within a core role and/or leading improvement initiatives. You will work with multiple customers and partners internally and externally across all phases of the drug development lifecycle, covering small and large molecule drug products. You will follow SHE and GMP standards and will be personally accountable for these areas within your own work plans.

Our Expectations

• Excellent communication skills.
• A scientific / business / supply chain management ambition.
• Organised and structured with an excellent aptitude for digital systems.
• Thrives in a process orientated workplace, on task-based activities and with a focus on the customer/patient.
• Team player with a problem-solving mindset and a focus on quality.
• Comfortable in a high paced and agile environment.
• Ability to reflect, see the bigger picture, whilst also having a focus on the detail.