Senior Validation Engineer - DeltaV & MES Expert

Bristol Myers Squibb; Harvard (MA); On-site; USD 92,000 - 112,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid holidays

Comprehensive benefits

Job summary

Bristol Myers Squibb is seeking a Senior Specialist, Validation Engineer - CSV in Devens, MA to qualify the DeltaV-based Process Control System and MES for GMP manufacturing. You will manage protocols, perform validation activities, and support cross-functional teams to ensure compliance and readiness for use.

The role emphasizes regulatory alignment, technical writing, and collaboration with stakeholders in a highly automated biologics facility.

Qualifications

• B.S. in engineering (chemical preferred) or equivalent.
• Knowledge of biopharmaceutical validation in GMP environment.

Responsibilities

• Validate GMP manufacturing systems (Process Automation & MES).
• Manage test protocol generation, execution, and reports for DeltaV and Syncade.
• Perform assessments and execute validation work from changes and projects.
• Provide validation support to multi-function teams and advise operations.

Skills

DeltaV

MES

Process automation

DCS/PLC

Regulatory/compliance (FDA/EU)

Project management

Technical writing

Education

B.S. in Engineering

Chemical engineering preferred

Tools

DeltaV

Syncade

Job description

Bristol Myers Squibb is seeking a Senior Specialist, Validation Engineer - CSV in Devens, MA to qualify the DeltaV-based Process Control System and MES for GMP manufacturing. You will manage protocols, perform validation activities, and support cross-functional teams to ensure compliance and readiness for use.

The role emphasizes regulatory alignment, technical writing, and collaboration with stakeholders in a highly automated biologics facility.