Senior Specialist Quality Assurance - 12 Month Secondment/FTC
UK Visa Sponsorship Analytics
Analytics are greyed out due to low classification confidence (28.0%).
Occupation Type
Quality assurance and regulatory professionals
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£48,200
(£24.72 per hour)
Occupation rate applies
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Description
Senior Specialist Quality Assurance – 12 Month Secondment/Fixed Term Contract
Macclesfield
Introduction To The Role
To provide QA expertise and support for manufacturing and packaging. To ensure that the manufacture and/or testing and operation of support systems meet all the regulatory and AstraZeneca standards and the appropriate level of compliance. This service must be delivered as efficiently as possible whilst still maintaining a reliable and robust output.
In this role, you will participate in quality initiatives and improvement projects to deliver enhanced compliance at a reduced cost. You will impact directly on the value stream by influencing decisions through advice to others. Responsible for the professional management of adverse events and all the associated quality management systems within the Process Execution Team (PET) you support.
The role available is within the QA team which supports our aseptic manufacturing area
The role may be required to work a day shift pattern with 1 weekend in 6.
What You'll Do
Macclesfield
Introduction To The Role
To provide QA expertise and support for manufacturing and packaging. To ensure that the manufacture and/or testing and operation of support systems meet all the regulatory and AstraZeneca standards and the appropriate level of compliance. This service must be delivered as efficiently as possible whilst still maintaining a reliable and robust output.
In this role, you will participate in quality initiatives and improvement projects to deliver enhanced compliance at a reduced cost. You will impact directly on the value stream by influencing decisions through advice to others. Responsible for the professional management of adverse events and all the associated quality management systems within the Process Execution Team (PET) you support.
The role available is within the QA team which supports our aseptic manufacturing area
The role may be required to work a day shift pattern with 1 weekend in 6.
What You'll Do
- You will be aligned to an aseptic manufacturing facility where you will be required to reinforce the quality principles. You will also provide independent assurance of the maintenance of the appropriate quality standards within this area, whilst supporting timely and effective resolution of all quality issues to maintain product flow across the factory.
- You'll be responsible for making product and material release decisions, operating within global standard pack ahead of clearance (PAOC) and ship ahead of clearance (SAOC) guidelines.
- Provide leadership and support for internal and external inspection preparations as well as significant audits to aid in developing improvement plans, you will monitor any actions to ensure ongoing compliance.
- You will provide expert advice to the area on Good Manufacturing Practice/Good Development Practice/Good Distribution Practice / Good Laboratory Practice within the site, with reference to Good Manufacturing Practice guidelines and regulations.
- Degree or equivalent professional qualification in a science / technical field such as Pharmacy, Chemistry or Biology (or equivalent experience)
- Significant experience in Good Manufacturing / Good Distribution / Good Laboratory practice and/or compliance management.
- Aseptic manufacture experience
- Previous experience in a role aligned to quality assurance.
- A level of technical process understanding in manufacturing or packing or warehouse/distribution or Quality Control
- Knowledge of and application of quality systems, including change control, deviation management and New Product Introductions
- Awareness / knowledge of regulatory interactions and compliance procedures and ability to apply this in an operations environment
- High level of customer focus and strong ability to reinforce and maintain quality standards.
- Knowledge of other areas of the Supply Chain, including groups such as Regulatory, Global Quality, Manufacturing, Supply and Capability etc.
- Good understanding of the Quality Management Systems (QMS) with experience in managing and/or approving deviation, documentation and change controls.
So, what’s next?
Are you already imagining yourself joining our team?
Good, because we can’t wait to hear from you.
Date Posted
16-Mar-2026
Closing Date
30-Mar-2026
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.
Are you already imagining yourself joining our team?
Good, because we can’t wait to hear from you.
Date Posted
16-Mar-2026
Closing Date
30-Mar-2026
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.