Specialist Quality Control (Analytical Molecular Bioassay)

## Explore a Rewarding Career in Quality Control at AstraZeneca (Speke, UK)

AstraZeneca, a global leader in biopharmaceuticals, is seeking a highly motivated and skilled Specialist Quality Control (Analytical Molecular Bioassay) to join their dynamic team at the Speke, Liverpool location. This is an exceptional opportunity for science-driven professionals to contribute to the development and delivery of life-changing medicines on a global scale.

If you are passionate about quality, thrive in a collaborative environment, and are eager to advance your career within a reputable pharmaceutical organization, this role presents a compelling prospect. The Speke site is a hub of innovation, producing up to 20 million vaccine doses annually, and fosters a strong sense of community and belonging among its employees.

Key Advantages for Aspiring Candidates:

• Impactful Work: Be at the forefront of ensuring the quality and efficacy of essential medicines, directly contributing to patient well-being worldwide.
• Lifelong Learning & Development: AstraZeneca is deeply committed to fostering continuous growth. You will have access to opportunities for ongoing learning, skill enhancement, and knowledge expansion, ensuring your career path remains dynamic and progressive.
• Cutting-Edge Environment: Work with a team that embraces innovation, employing the latest models and technologies to drive excellence in quality control processes. You will be exposed to and contribute to the scaling and implementation of new technologies.
• Collaborative Culture: Join a supportive community atmosphere where teamwork and cross-functional collaboration are paramount. Share expertise, offer support, and build strong professional networks across different sites and regions.
• Career Advancement: This role offers a clear path for career development within a leading biopharmaceutical company. The emphasis on accountability, brave decision-making, and a proactive, science-based approach to problem-solving prepares you for leadership opportunities.
• Structured Work Pattern: The 4 on 4 off, 12-hour day shift pattern provides a predictable and structured work schedule, allowing for effective work-life balance.

Key Considerations for Your Career Path:

• cGXP Expertise: A strong understanding and practical experience within a Good Manufacturing Practice (GMP) environment are essential. You will be responsible for conducting routine and non-routine investigational and validation testing in strict accordance with cGXP procedures.
• Analytical Skills: A degree or HND (or equivalent) in a scientific field is a prerequisite, alongside a solid grasp of Quality Control testing techniques. Your ability to perform detailed analytical work will be crucial.
• Problem-Solving & Investigation: This role requires a proactive, science-based, and solutions-oriented mindset. You will be expected to lead Quality Control investigations, identify root causes, and implement corrective actions.
• Regulatory Awareness: Support for regulatory inspections is a key accountability. Familiarity with regulatory compliance and maintaining meticulous documentation are vital.
• Health & Safety Commitment: Ensuring the compliance of all laboratory procedures and personnel with Health & Safety Guidelines is a non-negotiable aspect of this position.
• Biopharmaceutical Industry Experience: Previous experience within the biopharmaceutical sector is highly valued and will provide a strong foundation for success in this role.

This Specialist Quality Control position is an excellent opportunity for individuals seeking to make a tangible difference in the healthcare industry while embarking on a journey of continuous professional growth and development. If you are ready to embrace challenges, take ownership, and contribute to the mission of delivering life-changing medicines, we encourage you to apply.