At a Glance
- Tasks: Join a team transforming medicine through mRNA science and quality control.
- Company: Moderna, a leader in innovative healthcare solutions.
- Benefits: Top-notch healthcare, generous time off, and wellness support.
- Other info: Collaborative environment with opportunities for continuous learning and growth.
- Why this job: Make a real difference in patients' lives while advancing your career.
- Qualifications: BA/BSc in Chemistry preferred; 5-7 years in Quality Control.
The predicted salary is between 40000 - 50000 £ per year.
Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is establishing a leading research, development, and manufacturing facility at Harwell to support onshore mRNA vaccine production for respiratory diseases in the UK. This long‑term investment will create skilled jobs and strengthen collaboration with academic, NHS, and government partners. We welcome experts ready to help expand access to life‑saving vaccines.
This role sits at the intersection of Quality Control Chemistry and global stability programs, driving the analytical backbone that ensures product quality and compliance. It combines hands‑on laboratory execution with advanced data analysis, regulatory contribution, and digital system interaction. The position offers exposure to modern analytical platforms, LIMS ecosystems, and opportunities to work alongside emerging AI‑enabled tools in a highly innovative environment.
Here’s What You’ll Do
- Perform routine and advanced analytical chemistry and stability testing, including HPLC, UPLC, GC, UV, Dynamic Light Scattering (particle analysis), and Karl Fischer (KF).
- Execute HPLC (AEX) and NaOH plate reader–based assays to support manufacturing process statistical testing.
- Conduct testing across raw materials, components, in‑process materials, and drug substance samples.
- Maintain accurate and compliant cGMP documentation in alignment with Good Documentation Practices and Data Integrity requirements.
- Support end‑to‑end stability program activities, including sample set down, pulls, labeling, quantity verification, and inventory tracking using LIMS (LabVantage) and associated systems.
- Create, review, and revise stability protocols and reports in accordance with GMP, FDA, EU, and ICH guidelines.
- Build and maintain stability schedules, ensuring timely sample pulls and distribution to internal and external laboratories.
- Perform data trending and statistical analyses, maintaining up‑to‑date stability tables, charts, and databases.
- Execute stability study workflows within LIMS, including data entry, review, and approval.
- Support cross‑functional and external reporting of stability data, ensuring accuracy and completeness.
- Coordinate stability sample shipments to external laboratories and manage retrieval of external data and reports.
- Maintain internal stability binders and databases with up‑to‑date information from internal and external sources.
- Contribute to regulatory submissions through authoring and review of stability‑related sections.
- Carry out general laboratory operations including reagent preparation, sample management, equipment maintenance, and lab housekeeping.
- Maintain a safe and compliant laboratory environment aligned with GxP standards.
- Manage laboratory consumables, including ordering, stocking, and inventory control.
- Participate in quality systems activities including investigations, deviations, change controls, and CAPAs.
- Author and revise SOPs, protocols, and reports to support compliant operations.
- Support troubleshooting of analytical methods and laboratory equipment, while providing guidance and training to junior staff.
- Foster a collaborative, inclusive, and high‑performance team environment focused on innovation and continuous improvement.
- Execute all activities in accordance with SOPs, work instructions, regulatory requirements, and company policies.
- Complete all required training within defined timelines and maintain ongoing qualification readiness for audits and inspections.
The key Moderna Mindsets you’ll need to succeed in the role
- We obsess over learning. We don’t have to be the smartest; we have to learn the fastest.
- We digitize everywhere possible using the power of code to maximize our impact on patients.
Here’s What You’ll Need (Basic Qualifications)
- Education: BA/BSc in Chemistry (preferred) or other relevant scientific discipline.
- Experience: At least 5–7 years in Quality Control Laboratory of a Pharmaceutical Company.
- Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards).
As part of Moderna’s commitment to workplace safety, this role may require an enhanced pre‑employment check.
Pay & Benefits
- Best‑in‑class healthcare, plus voluntary benefit programs to support your unique needs.
- A holistic approach to well‑being with access to fitness, mindfulness, and mental health support.
- Family building benefits, including fertility, adoption, and surrogacy support.
- Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year‑end shutdown.
- Savings and investments to help you plan for the future.
- Location‑specific perks and extras.
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. Moderna is a smoke‑free, alcohol‑free, and drug‑free work environment. Moderna is committed to equal opportunity in employment and non‑discrimination for all employees and qualified applicants without regard to a person’s race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at leavesandaccommodations@modernatx.com.
(Fixed Term) Analyst, Quality Control, Chemistry & Stability in Oxford employer: Dormont Manufacturing Co
Moderna is an exceptional employer that fosters a culture of innovation and collaboration, particularly at our state-of-the-art facility in Harwell. Employees benefit from best-in-class healthcare, generous paid time off, and unique family-building support, all while contributing to life-saving mRNA vaccine production. With a strong emphasis on continuous learning and professional growth, this role offers the opportunity to work with cutting-edge technology in a supportive environment dedicated to making a real difference for patients.
StudySmarter Expert Advice🤫
We think this is how you could land (Fixed Term) Analyst, Quality Control, Chemistry & Stability in Oxford
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with current employees at Moderna. A friendly chat can sometimes lead to opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by diving deep into the role and the company. Understand their mission and how your skills in Quality Control Chemistry can make a difference. Tailor your answers to show you’re not just a fit, but the perfect fit!
✨Tip Number 3
Showcase your hands-on experience! Be ready to discuss specific projects or challenges you've tackled in the lab. Highlighting your analytical skills and familiarity with tools like HPLC and LIMS will definitely catch their attention.
✨Tip Number 4
Don’t forget to follow up after your interview! A quick thank-you email reiterating your enthusiasm for the role can leave a lasting impression. Plus, it shows you’re genuinely interested in joining the team at Moderna.
We think you need these skills to ace (Fixed Term) Analyst, Quality Control, Chemistry & Stability in Oxford
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Analyst in Quality Control. Highlight your experience with analytical chemistry and any relevant techniques like HPLC or UPLC. We want to see how your skills align with what we do at Moderna!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about mRNA science and how you can contribute to our mission. Keep it concise but impactful, and don’t forget to mention your understanding of GxP regulations.
Showcase Your Analytical Skills:In your application, be sure to showcase your analytical skills and any experience with data analysis or LIMS systems. We love candidates who can demonstrate their ability to drive product quality and compliance through data!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our innovative team!
How to prepare for a job interview at Dormont Manufacturing Co
✨Know Your Chemistry Inside Out
Make sure you brush up on your analytical chemistry skills, especially HPLC, UPLC, and GC. Be ready to discuss your hands-on experience with these techniques and how you've applied them in previous roles.
✨Familiarise Yourself with GxP Regulations
Since this role involves compliance with GxP standards, it’s crucial to understand GMP, GLP, and other relevant regulations. Prepare examples of how you've adhered to these standards in your past work.
✨Showcase Your Data Analysis Skills
This position requires advanced data analysis, so be prepared to discuss your experience with statistical analyses and data trending. Bring examples of how you've used data to drive decisions or improve processes.
✨Emphasise Team Collaboration
Moderna values a collaborative environment, so highlight your experience working in cross-functional teams. Share specific instances where you contributed to team success and how you fostered a positive team dynamic.