Senior Scientist, GMP Stability & Analytical Lead

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

Job summary

Bristol Myers Squibb in Moreton, UK is seeking an experienced Senior Scientist, Analytical Lead to drive GMP stability operations across development to clinical-stage products. You will own planning, documentation and inspection readiness while leading a team of scientists.

You will coordinate analytical activities, author validation protocols, support technology transfers, and partner with QA and project stakeholders to deliver timely, compliant results.

Qualifications

• Degree in analytical chemistry or related field (BSc or higher).
• Experience leading GMP stability operations across API or dosage forms.
• Strong knowledge of cGMP and data integrity for inspection readiness.
• Experience with HPLC, KF, and dissolution.
• Proven ability to manage multiple projects and stakeholders.

Responsibilities

• Lead GMP Stability Operations from development to clinical-stage products, planning, executing and documenting activities to cGMP standards.
• Coordinate analytical delivery, including validation protocols/reports and tech transfers; liaise with QA and project stakeholders.
• Coach and guide scientific staff to operate with high standards and effective collaboration.
• Own compliance and audit readiness to ensure inspection preparedness.
• Identify and implement improvements to stability operations and analytical delivery processes.

Skills

GMP stability operations

Analytical project delivery

Leadership / coaching

Quality Assurance & audits

Data integrity / cGMP knowledge

Education

BSc or higher in analytical chemistry or related field

Tools

HPLC

KF

Dissolution

Job description

Bristol Myers Squibb in Moreton, UK is seeking an experienced Senior Scientist, Analytical Lead to drive GMP stability operations across development to clinical-stage products. You will own planning, documentation and inspection readiness while leading a team of scientists.

You will coordinate analytical activities, author validation protocols, support technology transfers, and partner with QA and project stakeholders to deliver timely, compliant results.