Hybrid Senior Manager, QC Analytics – Cell Therapy

Bristol-Myers Squibb Co; Harvard (MA); Hybrid; USD 125,000 - 151,000; Full time

Job summary

Bristol Myers Squibb is seeking a Senior Manager, QC Analytical for the Cell Therapy Facility in Devens, MA. This hybrid role requires 50% onsite presence with flex hours, leading the QC Analytical team and driving KPIs and continuous improvement initiatives across the QC network.

You will oversee testing of clinical and commercial cell therapy products, manage personnel, ensure cGMP compliance, and communicate with cross-functional partners and senior management.

Qualifications

• Bachelor's degree or equivalent required, preferably in science; advanced degree preferred.
• 10+ years of relevant laboratory work experience, preferably in a regulated environment.
• 4+ years of management and people leader experience.
• Demonstrated success working in a high-performing, results-driven environment.

Responsibilities

• Lead the QC Analytical lab ensuring timely, efficient testing and data review for in-process, release, and stability testing.
• Develop, track, trend, and report KPIs for QC Analytical performance (e.g., turnaround time, right-first-time, backlog).
• Drive continuous improvement initiatives using operational excellence tools.
• Own one or more QC programs or functional areas and lead the team to develop and maintain the program.
• Hire, mentor, and develop team members to support business operations and career development.
• Communicate performance, risks, and resource needs to senior management.

Skills

Leadership

QC analytics

Regulatory compliance

Lean Six Sigma

Data analysis

Excel/Office tools

Cross-functional collaboration

Communication

Education

Bachelor's degree or equivalent

Advanced degree preferred

Tools

LIMS

ELN

DeltaV

SAP

Job description

Bristol Myers Squibb is seeking a Senior Manager, QC Analytical for the Cell Therapy Facility in Devens, MA. This hybrid role requires 50% onsite presence with flex hours, leading the QC Analytical team and driving KPIs and continuous improvement initiatives across the QC network.

You will oversee testing of clinical and commercial cell therapy products, manage personnel, ensure cGMP compliance, and communicate with cross-functional partners and senior management.