At a Glance
- Tasks: Ensure medicines are safe and effective by analysing stability data and writing protocols.
- Company: Join Bristol Myers Squibb, a leader in innovative medicine with a purpose-driven culture.
- Benefits: Enjoy comprehensive benefits, growth opportunities, and a supportive, inclusive work environment.
- Other info: Collaborate globally and develop your scientific credibility in a dynamic, evolving landscape.
- Why this job: Make a real impact on patients' lives while shaping the future of medicine.
- Qualifications: Degree in Analytical Chemistry or related field; 3-5 years in pharma industry preferred.
The predicted salary is between 37800 - 46200 £ per year.
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
At Bristol Myers Squibb, we're looking for a Stability Scientist to join our Analytical Science & Operations (ASO) team at our Moreton, UK site. This isn't just a role where you'll process data and file reports. This is a role where your scientific expertise directly shapes the path a medicine takes from development to the hands of the people who need it most.
So, what will you actually be doing? Think of yourself as the guardian of product integrity. You'll be working at the intersection of science, regulation, and strategy - ensuring that our drug substances and drug products remain safe and effective throughout their shelf life.
Here’s what that looks like day-to-day:
- You'll be the stability expert that CMC teams turn to when they need guidance to keep projects moving. Your knowledge unlocks progress.
- You'll write and approve stability protocols and reports — documents that directly support regulatory submissions for both small and large molecule therapies.
- You'll engage with global regulatory agencies — authoring responses to their questions and, at times, representing BMS directly in meetings.
- You'll analyse trends in stability data, raise the right flags at the right time, and make sure unexpected results get the attention they deserve.
- You'll shape how we work, evaluating and implementing changes that keep us aligned with evolving regulatory expectations and industry best practices.
- You'll keep us audit-ready, contributing to a culture of quality and compliance that BMS is known for globally.
And here's something worth noting: there is no laboratory bench work in this role. This is a science-driven, knowledge-based position focused on data, documentation, and decision-making.
What's in it for you?
- Broaden your scientific impact - You’ll work across both small and large molecule portfolios, giving you rare, cross‑functional exposure that many scientists spend years trying to achieve.
- Go global - Your work feeds directly into regulatory submissions worldwide.
- Build your influence - You won’t be working in a silo. You’ll be advising senior CMC teams, representing BMS in regulatory discussions, and collaborating across functions.
- Grow with the industry - The regulatory and scientific landscape is evolving fast - AI tools, modelling software, new ICH guidelines.
- Work in a culture of quality - Being audit‑ready isn't a tick‑box exercise here. It's a mindset.
Is this you?
You don't need to check every box, but here's the profile we have in mind:
- A degree in Analytical Chemistry, Chemistry, Biochemistry, or a related discipline (B.S. minimum)
- 3–5 years of pharmaceutical industry experience, ideally in a GMP environment
- A solid working knowledge of ICH guidelines and regulatory stability expectations
- Strong written communication skills - you can turn complex data into clear, compelling scientific narratives
- Comfortable working independently, managing timelines, and knowing when to elevate
- Familiar with Microsoft Office, and ideally systems like Veeva or LIMS
- Any exposure to AI tools, statistical, or modelling software? That's a genuine bonus here.
Why BMS? Why Moreton?
BMS is a company that lives its mission: transforming patients' lives through science. At our Moreton site, you'll be part of a team that combines the intimacy of a specialist facility with the resources and ambition of a global biopharma leader. You'll be surrounded by talented colleagues who care deeply about what they do and who understand that getting the science right isn't just professional pride, it's the difference between a medicine reaching a patient or not.
If you're ready to bring your stability expertise to work that truly matters - we'd love to hear from you.
We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume.
Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer.
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Pharmaceutical Development Stability Scientist employer: Bristol Myers Squibb
At Bristol Myers Squibb, we offer a unique opportunity for Integrated Healthcare Managers to engage in meaningful work that truly transforms lives. Our supportive culture fosters professional growth and innovation, while our competitive benefits ensure a healthy work-life balance. Join us in the South UK, where you can thrive in a dynamic environment alongside passionate colleagues dedicated to making a real difference in the field of haematology-oncology.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmaceutical Development Stability Scientist
✨Unlock Networking Opportunities
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Bristol Myers Squibb.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Bristol Myers Squibb. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Bristol Myers Squibb is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Pharmaceutical Development Stability Scientist
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 Bristol Myers Squibb!
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 Bristol Myers Squibb that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Bristol Myers Squibb!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Bristol Myers Squibb, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Bristol Myers Squibb
✨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 Bristol Myers Squibb that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
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 Bristol Myers Squibb’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.
✨Be Ready for Regulatory Scenarios
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.