At a Glance
- Tasks: Use mass spectrometry to quantify trace impurities and influence product strategies.
- Company: Join AstraZeneca, a leader in innovative medicines and inclusive culture.
- Benefits: Competitive salary, flexible working, and opportunities for professional growth.
- Other info: Collaborative environment with diverse teams and a focus on continuous improvement.
- Why this job: Make a real impact on patient safety and medicine development with cutting-edge science.
- Qualifications: Relevant scientific degree and experience in mass spectrometry required.
The predicted salary is between 54000 - 66000 £ per year.
This job is with AstraZeneca, an inclusive employer. Are you ready to use separation science and mass spectrometry to quantify trace impurities that protect patients and accelerate medicines to market? Based at our Macclesfield, UK campus, you will apply your expertise to generate decisive, high-quality data that directly shapes product understanding and control strategies.
You will join an analytical team that partners across development and commercialisation, translating complex trace-level signals into clear, evidence-led decisions. Your work will influence how products are designed, controlled and released, ensuring the right outcomes for patients and the business. Do you want to see your conclusions inform regulatory submissions and help define robust strategies for known and unknown impurities?
Accountabilities:
- Trace Impurity Quantification: Develop, review and apply mass spectrometry methods to quantify trace-level components in complex matrices, supporting both development projects and marketed products with reliable, sensitive and specific assays.
- Separation Science and Sample Preparation: Design and optimise sample-preparation and chromatographic approaches that resolve challenging low-level analytes, ensuring reproducible outcomes and robust method performance.
- Investigation and Characterisation: Investigate unexpected results and unknown impurities; conduct targeted characterisation and structure confirmation to explain signals and strengthen scientific rationale.
- Data Interpretation and Decision Influence: Translate analytical outputs into clear, defensible conclusions that drive product understanding, impurity control strategies and regulatory documentation.
- Cross-Functional Collaboration and External Oversight: Work closely with project teams and partner functions to deliver on timelines; transfer methods or oversee external laboratories to ensure consistent execution and data integrity.
- Quality, Compliance and Safety: Operate to Safety, Health and Environment expectations and applicable GMP, GLP and data-integrity standards; contribute to inspection-ready documentation and ways of working.
- Capability Building and Continuous Improvement: Share knowledge, mentor colleagues and advance scientific capability, including opportunities to apply automation and digital tools for efficiency and insight.
Essential Skills/Experience:
- A relevant scientific degree, or equivalent experience, with significant practical experience in mass spectrometry and pharmaceutical analysis.
- Demonstrated ability to develop, troubleshoot, review and apply mass spectrometry methods for the quantification of trace-level components in complex matrices.
- Practical experience operating and interpreting data from a range of mass spectrometry platforms, supported by strong separation-science and sample-preparation skills.
- Ability to interpret complex analytical data, draw scientifically defensible conclusions and communicate and influence effectively across disciplines, sites, cultures and external partners.
Desirable Skills/Experience:
- Experience with automated or high-throughput sample-preparation approaches and digital tools for analytical data processing or workflow improvement.
- Understanding of pharmaceutical product development, impurity control strategies and the development lifecycle from early development through launch and lifecycle management.
- Experience supporting method transfer, external analytical partners, technical investigations or regulatory submissions, and a proactive approach to developing colleagues.
- A sound understanding of quality and regulatory expectations relevant to pharmaceutical analysis, including GMP, data integrity and applicable ICH guidance.
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.
Why AstraZeneca:
Here you will build your expertise on a rich, science-led pipeline while working shoulder-to-shoulder with diverse experts who value evidence, accountability and modern approaches to Quality. We bring unexpected teams together to solve complex analytical problems, using advanced technologies and digital thinking to raise reliability and speed. Your data will carry the voice of the patient, informing control strategies that keep medicines safe and available worldwide. We value kindness alongside ambition, and we support bold, well-reasoned decisions that add real value across the product lifecycle.
What is next?
If you are ready to turn complex mass spectrometry challenges into decisions that safeguard patients and shape medicines, step forward and make your impact at AstraZeneca. We look forward to receiving your application not later than 5th November 2026.
Senior Scientist in Trace Analysis Mass Spectrometry in Warrington employer: AstraZeneca
AstraZeneca is an exceptional employer, offering a dynamic work environment in Cambridge where innovation meets collaboration. Employees benefit from a culture that values entrepreneurial thinking and scientific excellence, alongside opportunities for professional growth through mentorship and cross-functional projects. With a commitment to diversity and inclusion, AstraZeneca fosters a supportive atmosphere that empowers individuals to make meaningful contributions to life-changing medicines.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Scientist in Trace Analysis Mass Spectrometry in Warrington
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We think you need these skills to ace Senior Scientist in Trace Analysis Mass Spectrometry in Warrington
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at AstraZeneca!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show AstraZeneca that you're not just a fit for the job but also a safety-conscious candidate!
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How to prepare for a job interview at AstraZeneca
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at AstraZeneca that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with AstraZeneca’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.