Senior QA Engineering Lead - Equipment & Lab Validation

Bristol-Myers Squibb Co; Madison (NJ); On-site; USD 122,000 - 148,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid holidays

Medical, dental, vision benefits

Job summary

Bristol Myers Squibb Co in Madison, NJ is seeking a Senior Manager, QA Engineering (Equipment/Lab Methods/Utilities/Facilities) to oversee site validation and QC lab method validation in line with cGMP. You will lead calibration programs, qualification documentation, and data integrity initiatives while collaborating with cross-functional teams.

The role may be individual contributor or people manager, reporting to the Associate Director, QA Operations - Quality Engineering.

Qualifications

• Bachelor's degree in science or related field.
• Experience in pharmaceutical QA engineering is required.
• Strong documentation and approvals skills.

Responsibilities

• Oversee QA Engineering qualification activities for equipment, utilities and facilities.
• Ensure calibration/maintenance programs and validation plans are compliant.
• Lead data integrity initiatives and regulatory compliance.
• Manage the QA Engineering team and align with cross-functional partners.

Skills

GMP knowledge

Quality risk management

IQ/OQ/PQ protocols

Data integrity

Microsoft Office

Maximo

Education

Bachelor of Science

Tools

Maximo

BMSDocs

Infinity/Valgenesis

Job description

Bristol Myers Squibb Co in Madison, NJ is seeking a Senior Manager, QA Engineering (Equipment/Lab Methods/Utilities/Facilities) to oversee site validation and QC lab method validation in line with cGMP. You will lead calibration programs, qualification documentation, and data integrity initiatives while collaborating with cross-functional teams.

The role may be individual contributor or people manager, reporting to the Associate Director, QA Operations - Quality Engineering.