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- Tasks: Ensure quality assurance for drug substances and support clinical trial processes.
- Company: Join AstraZeneca, a leader in life-changing medicines with a diverse culture.
- Benefits: Hybrid working, competitive salary, and opportunities for professional growth.
- Other info: Inclusive workplace valuing diversity and offering excellent career development.
- Why this job: Make a real impact on patients' lives while working with innovative teams.
- Qualifications: 2-3 years in pharmaceutical GMP/GCP environments and a relevant scientific degree.
The predicted salary is between 30000 - 40000 £ per year.
Location – Macclesfield, UK
Hybrid Working - Min 3-4 days per week in HQ
Duration – 12 months
Inside IR35
Make a more meaningful impact to patients’ lives around the globe. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
In this role you will be responsible for QA release of Drug Substance and Investigational Medicinal Product for clinical trials. Provide input to support Packaging, Labelling & Distribution of IMP as required. In addition, you will support the delivery of QA activities for your assigned portfolio of projects and provide advice to support the development, implementation and continuous improvement of GMP quality systems across the development functions and support implementation of agreed global standards.
Essential Criteria- Appropriate scientific degree with experience (2-3 years) of working within a pharmaceutical GMP/GCP environment, preferably within a pharmaceutical development organisation
- A broad understanding of Quality Systems and GMP is essential
- An understanding of the pharmaceutical/drug development process
- Preferably have experience in Change Controls/Deviations/Batch Release
- Ideally - experience with development products IMP experience preferred
- Computer System Validation experience
- Supplier Manager experience from a quality assurance perspective
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. 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 from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
Closing Date for Advert - Monday 18th May - Applications will be reviewed from this date.
Quality Assurance Specialist in Warrington employer: AstraZeneca
Contact Detail:
AstraZeneca Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist in Warrington
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with current employees at the company. A friendly chat can sometimes lead to opportunities that aren’t even advertised!
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to Quality Assurance. We recommend using the STAR method (Situation, Task, Action, Result) to structure your answers and showcase your experience effectively.
✨Tip Number 3
Show your passion for the role! When you get the chance to speak with interviewers, let them know why you’re excited about making an impact in patients’ lives through quality assurance. Your enthusiasm can set you apart from other candidates.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our unique and ambitious team.
We think you need these skills to ace Quality Assurance Specialist in Warrington
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Assurance Specialist role. Highlight your relevant experience in GMP/GCP environments and any specific projects you've worked on that align with the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance and how your background makes you a perfect fit for our team. Don’t forget to mention your understanding of the pharmaceutical development process!
Showcase Your Skills: Be sure to showcase your skills related to Quality Systems, Change Controls, and Batch Release. We want to see how your expertise can contribute to our mission of making a meaningful impact on patients’ lives.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and get you one step closer to joining our ambitious team!
How to prepare for a job interview at AstraZeneca
✨Know Your Quality Systems
Make sure you brush up on your knowledge of Quality Systems and GMP. Be ready to discuss how your experience aligns with the requirements of the role, especially in relation to Change Controls and Batch Release. This will show that you understand the core responsibilities of a Quality Assurance Specialist.
✨Showcase Your Experience
Prepare specific examples from your past roles that demonstrate your experience in a pharmaceutical GMP/GCP environment. Highlight any projects where you contributed to the QA release of Drug Substances or Investigational Medicinal Products, as this will resonate well with the interviewers.
✨Emphasise Team Collaboration
Since the company values teamwork and collaboration, be ready to share instances where you worked effectively within a team. Discuss how you’ve contributed to bold thinking and innovative solutions in previous roles, as this aligns with their mission to inspire life-changing medicines.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to quality assurance and their expectations for the role. This not only shows your interest but also gives you a chance to assess if the company culture and values align with your own, especially regarding flexibility and inclusivity.