Quality Control Analyst (Analytical Molecular Bioassay)

AstraZeneca; Liverpool; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading biopharmaceutical company in Liverpool is seeking a Quality Control Analyst to conduct investigational and validation testing. You will ensure compliance with cGXP and GMP guidelines and support regulatory inspections. A degree in a scientific field is required, along with experience in a GMP environment. This role follows a 4 on 4 off, 12-hour shift pattern. Join a mission to deliver life-changing medicines.

Qualifications

• Qualified to degree level or equivalent in a scientific field.
• Experience in a Good Manufacturing Practice environment.
• Understanding of Quality Control testing techniques.

Responsibilities

• Conduct routine and non-routine testing in compliance with cGXP procedures.
• Lead Quality Control investigations and support regulatory inspections.
• Update GMP documents and ensure compliance with Health & Safety Guidelines.

Skills

GMP experience

GLP experience

Quality Control testing techniques

Biopharmaceutical Industry experience

Education

Degree level/HND in a scientific field

Job description

Job Description:

Job information Quality Control Analyst (Analytical Molecular Bioassay) from the Company AstraZeneca, this latest Quality Control Analyst (Analytical Molecular Bioassay) job vacancy is located in the city Liverpool L located in the country United Kingdom . This latest job opening is open to job seekers who have the latest education / graduate GCSE .

Job Responsibility:

Quality Control Analyst (Analytical Molecular Bioassay)

Location: Speke Liverpool

Join us at AstraZeneca's Speke location in the UK, where we are committed to unlocking opportunities for lifelong learning and development. We are a team that never stands still, constantly growing our abilities, skills, and knowledge. Our work is inspiring and rewarding, influencing every part of the product lifecycle to deliver life-changing medicines.

At Speke, we research, develop, produce and distribute up to 20 million vaccine doses a year for the global market. Join us and be part of a community atmosphere where everyone feels welcome!

Accountabilities:

As a Quality Control Analyst, you will conduct routine and non-routine investigational and validation testing on products in accordance with the appropriate cGXP procedures, GMP Compliance Rulebook, the Code of Conduct, quality manual and any other company policies. You will provide support to regulatory inspections, lead Quality Control investigations, update GMP documents within the appropriate system, and ensure the compliance of all laboratory procedures and personnel with Health & Safety Guidelines.

Essential skills/experience:

• Qualified to degree level/HND or equivalent in a scientific field
• Experience in a Good Manufacturing Practice (GMP) environment / Good Laboratory Practice (GLP)
• Understanding of Quality Control testing techniques
• Previous Biopharmaceutical Industry experience

This position will operate a 4 on 4 off, 12 hour days shift pattern.

At AstraZeneca, we take Quality seriously. We are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes. We are proactive, science-based, and solutions-oriented. Our focus is on scaling and introducing new technologies, using models to predict and proactively manage risk. We work cross-functionally, across sites and regionally, sharing expertise and offering support to others. We are strong communicators and networkers who take personal responsibility for the outcomes.

Join us at AstraZeneca's Operations team and pioneer a new' Quality way. Develop your expertise by being both challenged and supported to apply a modern' Quality mindset. It means taking accountability and making brave decisions. Whether that's reimagining the best way to respond to procedures and regulations, or pushing back when there's disagreement.

AstraZeneca is an equal opportunities employer. We welcome applications from all sections of the community. All applicants will be judged on their individual merits and qualifications, regardless of race, gender, age, disability, sexual orientation, religion or belief.

Are you ready to make a difference? Apply now and join us in our mission to deliver life-changing medicines!

Note: Applications will be accepted until 2025-11-02.