At a Glance
- Tasks: Ensure quality assurance for drug substances and investigational medicinal products in clinical trials.
- Company: Join AstraZeneca, a leader in life-changing medicines with a diverse and inclusive culture.
- Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
- Other info: Embrace diversity and inclusion in a dynamic workplace with excellent career prospects.
- Why this job: Make a real impact on patients' lives while working with innovative teams.
- Qualifications: 2-3 years experience in pharmaceutical GMP/GCP environments and a relevant scientific degree.
The predicted salary is between 40000 - 50000 £ 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 is preferable. Experience in Change Controls/ Deviations/ Batch Release is ideal. 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.
Pharma QA Release Specialist — Hybrid, 12-Month Role in Macclesfield employer: AstraZeneca
AstraZeneca is an exceptional employer that fosters a collaborative and inclusive work culture, where diverse teams come together to drive innovative solutions in the pharmaceutical industry. With a strong commitment to employee growth, we offer opportunities for professional development while maintaining a flexible hybrid working model that balances in-office collaboration with personal flexibility. Join us in making a meaningful impact on patients' lives globally, all while being part of a supportive environment that values your unique contributions.
StudySmarter Expert Advice🤫
We think this is how you could land Pharma QA Release Specialist — Hybrid, 12-Month Role in Macclesfield
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharma industry, especially those who work at companies you're interested in. A friendly chat can lead to insider info and even referrals that could get your foot in the door.
✨Tip Number 2
Prepare for those interviews! Research the company’s recent projects and their impact on patients. Show them you’re not just another candidate; you’re genuinely excited about contributing to their mission of life-changing medicines.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website! We love seeing applications directly from candidates who are keen on joining us. It shows initiative and gives you a better chance of standing out in the crowd.
We think you need these skills to ace Pharma QA Release Specialist — Hybrid, 12-Month Role in Macclesfield
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences that match the Pharma QA Release Specialist role. Highlight your experience in GMP/GCP environments and any relevant projects you've worked on.
Craft a Compelling Cover Letter:Use your cover letter to tell us 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 Team Spirit:Since we value collaboration, mention any experiences where you’ve worked effectively in teams. Highlight how you’ve contributed to group success, especially in fast-paced environments like clinical trials.
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of being noticed. It’s the easiest way for us to keep track of your application and ensure it gets to the right people!
How to prepare for a job interview at AstraZeneca
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP). Be ready to discuss how these principles apply to the QA release process, as well as any relevant experiences you've had in a pharmaceutical environment.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've handled change controls, deviations, or batch releases in the past. Highlight your ability to think critically and provide solutions that align with quality standards, as this will demonstrate your readiness for the role.
✨Understand the Drug Development Process
Familiarise yourself with the pharmaceutical/drug development process. Be prepared to discuss how your previous experience relates to this process and how you can contribute to the continuous improvement of quality systems within the company.
✨Emphasise Team Collaboration
Since the role involves working closely with various teams, be ready to talk about your experience in collaborative environments. Share specific instances where teamwork led to successful outcomes, especially in relation to QA activities and project delivery.
