Senior Analytical Lead, GMP Stability & Compliance

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

Job summary

Bristol Myers Squibb at the Moreton site seeks an experienced Senior Scientist, Analytical Lead, to own GMP stability operations end-to-end, from sample management to regulatory readiness. You will oversee analytical project delivery and drive cross-functional collaboration with QA and development teams.

You'll coach scientific staff, foster robust processes, and ensure compliance in a regulated environment.

Qualifications

• A degree in analytical chemistry, chemistry, biochemistry or a related field (BSc or higher).
• Hands-on experience leading or coordinating GMP stability operations across API, drug product intermediates and/or oral solid dosage forms.
• Strong working knowledge of cGMP, data integrity and what inspection readiness actually looks like in practice.
• Experience with HPLC, KF, dissolution and analytical method validation.
• A track record of juggling multiple projects, deadlines and stakeholders without dropping the ball.
• The confidence to operate with minimal supervision and the judgment to know when to elevate.
• A natural ability to bring people with you, through coaching or influencing.

Responsibilities

• Lead GMP Stability Operations, owning stability sample operations from development through to clinical-stage products.
• Drive Analytical Project Delivery, coordinating activities across deliverables and authoring validation protocols and reports.
• Coach and guide scientific staff, building consistent ways of working and high performance.
• Own compliance and audit readiness, applying risk management to stay inspection-ready.

Skills

Leadership

Project coordination

Regulatory awareness

Education

Analytical chemistry degree or related field

Tools

HPLC

KF

Dissolution

Analytical method validation

Job description

Bristol Myers Squibb at the Moreton site seeks an experienced Senior Scientist, Analytical Lead, to own GMP stability operations end-to-end, from sample management to regulatory readiness. You will oversee analytical project delivery and drive cross-functional collaboration with QA and development teams.

You'll coach scientific staff, foster robust processes, and ensure compliance in a regulated environment.