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- Tasks: Support clinical supply management with quality events and compliance activities.
- Company: Join AstraZeneca, a global leader in innovative medicines.
- Benefits: Flexible working options, competitive pay, and a vibrant work culture.
- Why this job: Make a real impact in drug development while learning from industry experts.
- Qualifications: Experience in a GXP environment and a passion for quality processes.
- Other info: Dynamic team environment with opportunities for growth and development.
The predicted salary is between 30000 - 42000 £ per year.
Job Description
Role: Clinical Supply Quality Events Associate
Role Type: Temporary
Location: Macclesfield (First 3 months, will be 5 days per week on-site. 3 Months onwards – x3 days on-site + 2 working remote per week).
Your New Company:
At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.
In Pharmaceutical Technology and Development (PT&D), we are the bridge between brilliant science and innovative medicines that help millions of people. We work across the entire value chain, designing 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.
The Clinical Supply Quality Events Associate supports the clinical supply management team with task-based activities relating to quality events i.e. Deviations and Product Quality Complaints, to ensure compliance in the delivery of materials to clinical trial patients.
This role is a great opportunity for someone who wishes to develop their quality and compliance understanding in the agile, vibrant and global environment of clinical supply management.
What You Will Do
- Document the intake of Product Quality Complaints and Deviations ensuring they are reported in the Enterprise Quality Vault within expected timelines.
- Coordinate sample returns of Product Quality Complaints.
- Monitor the incoming Product Quality Complaints and ensure they are attended to by the global team.
- Support the Clinical Supply Quality Events Lead in preparing for and facilitating the weekly Pulses meeting.
- Facilitation of Deviation Investigations.
- Quality Events quarterly review data retrieval and presentation preparation.
- Develop process standards and training material around Quality Event Management.
- Ad hoc support with task-based activities to support the Global Clinical Supply Associate Team.
In this role you will have the opportunity to 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.
Essential Skills
- Experience of working in a GXP environment up to 2 years
- Organized and structured with an excellent aptitude for digital systems.
- Excellent time management and ability to meet agreed timelines.
- A team player who is comfortable in a high paced and agile working environment.
- Academic degree in a scientific discipline or supply chain management
- Passion for Quality and Processes
WHY ASTRAZENECA?
It's an exciting time to join AstraZeneca, a global business that's rapidly growing – there's a lot happening and even more to come. And we are a valued part of this journey. Respected partners across the business, we provide the platform that's going to power us to achieve more.
So, what's next?
Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours. Please apply with a copy of your CV.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team regardless of their characteristics. We align with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification
Clinical Supply Quality - Events Associate employer: AstraZeneca
Contact Detail:
AstraZeneca Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Supply Quality - Events Associate
✨Tip Number 1
Get to know AstraZeneca! Research their values and recent projects. This will help you tailor your conversations and show that you're genuinely interested in being part of their mission.
✨Tip Number 2
Network like a pro! Connect with current employees on LinkedIn or attend industry events. A friendly chat can sometimes lead to insider tips or even a referral!
✨Tip Number 3
Prepare for the interview by practising common questions related to quality management and compliance. Use the STAR method to structure your answers and highlight your relevant experience.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining the team at AstraZeneca.
We think you need these skills to ace Clinical Supply Quality - Events Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Clinical Supply Quality Events Associate role. Highlight any experience in GXP environments and your passion for quality and processes.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're excited about this role at AstraZeneca. Share specific examples of how your background aligns with our mission to put patients first and your ability to thrive in a fast-paced environment.
Showcase Your Organisational Skills: Since this role requires excellent time management and organisation, make sure to highlight any relevant experiences where you've successfully managed multiple tasks or projects. We love seeing how you keep things on track!
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. We can’t wait to see what you bring to the table!
How to prepare for a job interview at AstraZeneca
✨Know Your Quality Events
Familiarise yourself with the key concepts of quality events, such as Product Quality Complaints and Deviations. Be ready to discuss how you would document and manage these events, as this will show your understanding of the role and its importance in clinical supply management.
✨Showcase Your Organisational Skills
Since the role requires excellent time management and organisation, prepare examples from your past experiences where you successfully managed multiple tasks or projects. Highlight any digital systems you've used to streamline processes, as this aligns with what AstraZeneca is looking for.
✨Emphasise Team Collaboration
AstraZeneca values teamwork, so be prepared to share instances where you worked effectively within a team, especially in high-paced environments. Discuss how you contributed to achieving common goals and how you handle challenges collaboratively.
✨Demonstrate Your Passion for Quality
Express your enthusiasm for quality and compliance in the pharmaceutical industry. Share any relevant experiences or coursework that reflect your commitment to maintaining high standards, and be ready to discuss how you can contribute to AstraZeneca's mission of putting patients first.