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Senior Specialist Quality Control

Ort Liverpool, England, Vereinigtes Königreich Anzeigen-ID R-223748 Veröffentlichungsdatum 04/04/2025

Senior Specialist Quality Control

Location: Liverpool

Type: Permanent

Competative salary and benefits

Introduction to role

As the voice of the patient, every batch we certify is a personal stamp of approval. Not something we take lightly, we are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes. As QC Virology Senior Specialist, you will act as a subject matter expert within QC Virology providing technical and analytical support to the Quality Control function within the Speke site in addition to the wider site and global AZ partners.

Accountabilities

You'll be responsible for instrumentation and methodology troubleshooting, non-routine analysis, and the evaluation, exploitation and implementation of new technology. You'll lead significant Quality Control investigations and change programs including introduction of new methods and technologies. You will have expert knowledge and understanding of the functional area and laboratory instrumentation, as well as Good Manufacturing Practice/Good Laboratory Practice. We'll look to you to play a key role in coaching and mentoring and developing other team members and working cross departmentally to support the overall QC organisation.

Essential Skills/Experience

• Qualified to degree level/or equivalent in a scientific area

• Technical SME in a QC Field (or equivalent)

• Effective problem solving skills.

• Leading change and digital uplift (focussing on optimising of QC assays)

• Working collaboratively with regulatory and understanding of new market launches

•Experience in investigating complex investigations

•Audit experience

•Can work collaboratively with key stakeholders

• Sound knowledge and understanding of the principles and concepts of compliance management and Good Manufacturing Practice / Good Laboratory Practice

• Knowledge and understanding of Quality systems such as Qualification/Validation, Change Management, Quality Risk Management

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.

At AstraZeneca, our work is important and valued. We are proactive, science-based, and solutions-oriented, always striving to make a significant impact on patients' lives. Our inclusive and friendly community fosters collaboration and innovation, ensuring that each voice matters. With a focus on growth and innovation, there are always exciting opportunities to quality assure new products as we go to market around the world.

Ready to make a difference? Apply now to join our team!



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