Global Stability Scientist - Regulatory & CMC Expert

Bristol Myers Squibb; Wirral; On-site; GBP 65,000 - 90,000; Full time

Job summary

Bristol Myers Squibb in the UK is seeking a Pharmaceutical Development Stability Scientist to safeguard product integrity across small and large molecule programs. You will work at the intersection of science, regulation, and strategy to ensure drug substances remain safe and effective through shelf life.

No lab bench work here; you will prepare stability protocols and reports for regulatory submissions, engage with global agencies, analyze data trends, and drive improvements in line with

Qualifications

• Degree in Analytical Chemistry, Chemistry, Biochemistry, or related discipline (BS minimum).
• 3–5 years of pharmaceutical industry experience in GMP environment.
• Solid knowledge of ICH guidelines and regulatory stability expectations.
• Strong written communication skills; ability to turn complex data into clear scientific narratives.
• Familiar with Microsoft Office; ideally Veeva or LIMS; exposure to AI tools or modelling software is a bonus.

Responsibilities

• Be the stability expert for CMC teams to keep projects moving.
• Write and approve stability protocols and reports for regulatory submissions.
• Engage with global regulatory agencies and represent BMS in meetings.
• Analyse stability data trends, raise flags early, and ensure timely attention to results.
• Shape our processes by evaluating changes to stay aligned with evolving regulatory expectations.
• Maintain audit readiness and contribute to a culture of quality and compliance.

Skills

Written communication

Independent worker

Timeline management

Cross-functional collaboration

Education

Analytical Chemistry, Chemistry, Biochemistry, or related discipline (BS minimum)

Tools

Veeva

LIMS

Microsoft Office

Job description

Bristol Myers Squibb in the UK is seeking a Pharmaceutical Development Stability Scientist to safeguard product integrity across small and large molecule programs. You will work at the intersection of science, regulation, and strategy to ensure drug substances remain safe and effective through shelf life.

No lab bench work here; you will prepare stability protocols and reports for regulatory submissions, engage with global agencies, analyze data trends, and drive improvements in line with