Senior Process Engineer – Pharma Scale-Up & CDMO Partnerships

Bristol Myers Squibb EU Policy; Wirral; Hybrid; GBP 70,000 - 110,000; Full time

Benefits offered by this job

Remote work up to 50%

Travel up to 20%

Four work models

Job summary

Bristol Myers Squibb is seeking a highly experienced Process Engineer to join the Chemical Process Development (CPD) team in Moreton, UK. The role focuses on translating lab-scale chemistry into scalable manufacturing processes for clinical supplies and ADCs, with a strong emphasis on safety, quality, and collaboration with external CDMOs.

Your background includes a B.Eng./M.Eng. in Chemical Engineering and 10–15 years in industrial manufacturing, preferably in GMP environments.

Qualifications

• Bachelor’s or Master’s degree in Chemical Engineering.
• Extensive experience in industrial manufacturing, GMP environments.
• Ability to read lab protocols and translate them to manufacturing plans.

Responsibilities

• Review batch records for hazardous chemistry campaigns to ensure safety, quality, and process feasibility.
• Assess CDMO facilities to verify equipment and capabilities, and specify changes if needed.
• Troubleshoot manufacturing issues using engineering fundamentals and cross-functional collaboration.
• Present risk assessments and recommendations to leadership in clear, actionable terms.
• Build and maintain strong relationships with CDMO partners across the world to support collaboration.

Skills

Chemical engineering fundamentals

Read lab protocols

Cross-functional collaboration

Scale-up risk assessment

Education

B.Eng./M.Eng. in Chemical Engineering

Job description

Bristol Myers Squibb is seeking a highly experienced Process Engineer to join the Chemical Process Development (CPD) team in Moreton, UK. The role focuses on translating lab-scale chemistry into scalable manufacturing processes for clinical supplies and ADCs, with a strong emphasis on safety, quality, and collaboration with external CDMOs.

Your background includes a B.Eng./M.Eng. in Chemical Engineering and 10–15 years in industrial manufacturing, preferably in GMP environments.