Specialist Quality Control

Specialist Quality Control

Speke, Liverpool

Shift – 4 days on, 4 days off

Job Description

The Specialist Quality Control is responsible for performing tests, analyses, and procedures in the laboratory, ensuring compliance with requirements, policies, procedures, and standards. Responsibilities include but are not limited to:

• Performing quality control testing for materials, samples, and products.
• Ensuring all laboratory activities and documentation comply with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Troubleshooting analytical equipment and test methods, as required.
• Preparing and reviewing laboratory documentation, including test records, reports, and protocols.
• Participating in investigations relating to out-of-specification or atypical results and supporting corrective and preventive actions.
• Assisting in the implementation and maintenance of laboratory systems and performance monitoring.
• Facilitating training for new staff or technicians on relevant laboratory practices and procedures.
• Collaborating closely with cross-functional teams to ensure timely testing, release, and disposition of products.
• Supporting improvement initiatives and participating in projects sought at improving laboratory efficiency and compliance.

Essential Criteria

• Bachelor’s degree or equivalent experience in a scientific field, preferably Chemistry, Biochemistry, or Pharmaceutical Sciences.
• Experience in a pharmaceutical, biotechnology, or related industry laboratory environment.
• Proven knowledge of laboratory techniques, equipment operation, and regulatory compliance.
• Strong written and verbal communication skills; ability to generate technical documentation.
• Ability to work independently and collaboratively in a fast-paced environment.
• Thorough with strong organizational, analytical, and problem-solving skills.

Desired Criteria

• Experience with cell culture methods.
• Previous experience in a QC role within a regulated manufacturing environment.
• Familiarity with LIMS and other electronic laboratory systems.
• Knowledge of international regulatory expectations (e.g., FDA, EMA).

At AstraZeneca, our work is important and valued. Our approach involves being forward-thinking, science-driven, and dedicated to positively affecting patients. 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

29-Aug-2025

Closing Date

04-Sept-2025

Our 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 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 authorisation and employment eligibility verification requirements.