Lead, Separations & Analytical Sciences

Bristol Myers Squibb; Harvard (MA); On-site; USD 174,000 - 211,000; Full time

Benefits offered by this job

Health Coverage

Wellbeing Programs

401(k)

Job summary

Bristol Myers Squibb in Devens, MA is seeking an Associate Director of Separations within Analytical Method Sciences to lead analytical lifecycle activities for biologics, including method development, transfer, validation, and lifecycle management across GMP programs.

You will build a high-performing team, set scientific priorities, partner with QC, Regulatory, Manufacturing and MS&T, and drive strategy, risk governance, and regulatory submissions while upholding quality and compliance.

Qualifications

• PhD in Chemistry or related field with 10+ years of industry experience.
• Significant experience in analytical sciences supporting biologics development and commercialization.
• Experience authoring and supporting regulatory submissions and inspections.
• Proven leadership of scientific teams in regulated environments.

Responsibilities

• Lead analytical lifecycle activities for separations methods across GMP programs.
• Strategic leadership for method development, validation, transfer, and monitoring.
• Partner with QC, Regulatory, Manufacturing, and MS&T teams to align analytical strategies.
• Coach scientists, manage priorities, and drive continuous improvement.

Skills

Analytical leadership

Team leadership

Regulatory submissions

Lifecycle management

cGMP/Regulatory

Problem solving

Education

PhD in Chemistry or related field

Tools

SEC

CEX

CE-SDS

icIEF

Peptide mapping

Glycan analysis

Job description

Bristol Myers Squibb in Devens, MA is seeking an Associate Director of Separations within Analytical Method Sciences to lead analytical lifecycle activities for biologics, including method development, transfer, validation, and lifecycle management across GMP programs.

You will build a high-performing team, set scientific priorities, partner with QC, Regulatory, Manufacturing and MS&T, and drive strategy, risk governance, and regulatory submissions while upholding quality and compliance.