Senior Specialist Quality Control

Liverpool, United Kingdom

Job Description


Senior Specialist Quality ControlLocation: LiverpoolType: PermanentCompetative salary and benefitsIntroduction to roleAs 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.AccountabilitiesYou'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!Date Posted 04-Apr-2025Closing Date 16-Apr-2025Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

AstraZeneca

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Job Detail

  • Job Id
    JD3029819
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Liverpool, United Kingdom
  • Education
    Not mentioned