Pharmaceutical Development Stability Scientist

Job description

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. Have you ever thought about the journey a medicine takes before it reaches a patient? Behind every approved therapy is a team of scientists who made sure it was safe, stable, and ready - that could be you. 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. That's real visibility on an international stage. - **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 — because catching an issue early can make all the difference. - **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. **W****hat's in it for you?** Let's be direct about the value this role adds to *your* career: - **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**. Seeing your name on documents that shape international approvals? That's a career highlight you'll carry for life. - **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. Your voice will matter. - **Grow with the industry** - The regulatory and scientific landscape is evolving fast - AI tools, modelling software, new ICH guidelines. In this role, you'll be right at the frontier of those changes, not playing catch-up. - **Work in a culture of quality** - Being audit-ready isn't a tick-box exercise here. It's a mindset. You'll develop rigorous professional habits that will define your scientific credibility for the rest of your career. **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 escalate - 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.** *Apply now and take the next step in a career where your science has real-world impact.* *#LI-Hybrid* We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. **How We Work** 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. Learn more at . **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. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [adastaffingsupport@bms.com](mailto:adastaffingsupport@bms.com). Visit [](https://careers.bms.com/eeo-accessibility) to access our complete Equal Employment Opportunity statement. Bristol Myers Squibb is Disability Confident – Employer A UK Government scheme **Candidate Rights** BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: **Data Protection** We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at [](http://careers.bms.com/fraud-protection). Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at [TAEnablement@bms.com](mailto:TAEnablement@bms.com) with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account. R1605484 : Pharmaceutical Development Stability Scientist