Cell Therapy QA Shop Floor Specialist

Bristol Myers Squibb; Harvard (MA); On-site; USD 90,000 - 109,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible Time Off

Paid vacation

Job summary

Bristol Myers Squibb is seeking a Senior Specialist, QA Shop Floor in Devens, MA. The role supports 24x7 quality collaboration across manufacturing, QC and warehouse operations on a Monday–Friday day schedule.

You will monitor process performance, own quality system records, and partner with multiple teams to ensure compliance with policies and GMP standards. Strong data skills and doc control experience are essential.

Qualifications

• Able to interpret internal SOPs, policies and regulatory guidelines.
• Proficient with digital tools (MS Office, etc.) and learning new software.
• Strong written and verbal communication for technical data.
• Ability to work in fast-paced team and lead peers through changing priorities.
• Detail-oriented with focus on deadlines and prioritization.
• Ability to negotiate and influence for mutual solutions.

Responsibilities

• Provide quality oversight to manufacturing, QC, and warehouse operations.
• Review or approve GMP records including procedures, CAPAs, changes, deviations.
• Lead area walkthroughs, identify quality issues and drive remediation plans.
• Prepare and approve procedural documents and training content.
• Coordinate with cross-functional teams and present topics during audits.

Skills

Data interpretation

Documentation

Quality systems

Communication

Team leadership

Education

Bachelor's degree in STEM

Associates/HS diploma alternative

Tools

MS Office

Power Automate

Smartsheet

Tableau

SAP

MES

Job description

Bristol Myers Squibb is seeking a Senior Specialist, QA Shop Floor in Devens, MA. The role supports 24x7 quality collaboration across manufacturing, QC and warehouse operations on a Monday–Friday day schedule.

You will monitor process performance, own quality system records, and partner with multiple teams to ensure compliance with policies and GMP standards. Strong data skills and doc control experience are essential.