At a Glance
- Tasks: Ensure quality assurance for drug substances and support clinical trial processes.
- Company: Join a leading pharmaceutical company making a global impact.
- Benefits: Hybrid working, competitive salary, and opportunities for professional growth.
- Other info: Diverse and inclusive workplace committed to equality and innovation.
- Why this job: Make a difference in patients' lives while developing your career in a dynamic environment.
- Qualifications: Scientific degree with 2-3 years in a GMP/GCP pharmaceutical setting.
The predicted salary is between 28800 - 43200 £ per year.
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 of Packaging, Labelling & Distribution of IMP as required. In addition, you will support the delivery of QA activities for their 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.
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.
Preferable have experience in Change Controls/ Deviations/ Batch Release.
Ideally - experience with development products.
IMP experience preferred.
- 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 Macclesfield employer: AstraZeneca
At AstraZeneca, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of Macclesfield. With a commitment to employee growth, we provide ample opportunities for professional development while maintaining a flexible hybrid working model that respects individual needs. Join us to make a meaningful impact on patients' lives and be part of a diverse team dedicated to pushing the boundaries of pharmaceutical excellence.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Assurance Specialist in Macclesfield
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their values and how they align with your own. This will help you stand out and show that you're genuinely interested in being part of their team.
✨Tip Number 3
Practice common interview questions and scenarios related to Quality Assurance. Use the STAR method (Situation, Task, Action, Result) to structure your answers. This will help you articulate your experience clearly and confidently.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive about joining our team.
We think you need these skills to ace Quality Assurance Specialist in Macclesfield
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Assurance Specialist role. Highlight your experience in GMP/GCP environments and any relevant projects you've worked on. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in the pharmaceutical industry. Share specific examples of how you've contributed to quality systems or improvements in past roles.
Showcase Your Skills:Don’t forget to showcase your skills related to Change Controls, Deviations, and Batch Release. We’re looking for candidates who can demonstrate their understanding of these processes and how they’ve applied them in real-world scenarios.
Apply Through Our Website:We encourage you to apply through our website for the best chance of being noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing applications come directly from our site!
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 you've applied these in your previous roles, especially in a pharmaceutical environment. This will show that you understand the core responsibilities of the Quality Assurance Specialist position.
✨Showcase Your Experience
Prepare specific examples from your past work that highlight your experience with Change Controls, Deviations, and Batch Release. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easier for the interviewer to see your impact.
✨Emphasise Team Collaboration
Since the role involves working closely with various teams, be ready to talk about how you’ve successfully collaborated in the past. Share instances where you’ve contributed to team success or helped resolve conflicts, showcasing your ability to work in a hybrid environment.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to continuous improvement in GMP quality systems. This not only shows your interest in the role but also demonstrates your proactive mindset and eagerness to contribute to their ambitious goals.
