QA Engineering Manager – Equipment & Facilities

Bristol-Myers Squibb; United States; On-site; USD 120,000 - 180,000; Full time

Job summary

Bristol Myers Squibb is seeking a Manager, QA Engineering (Equipment/Lab Methods/Utilities/Facilities) to oversee site technology transfer activities in a fast-paced manufacturing facility producing CAR T and drugs.

The role covers review of validation/qualification docs, change controls, and investigations with CAPA. It may be individual contributor or people manager, guiding cross-functional teams and ensuring data integrity per global standards.

Qualifications

• Must have GMP, Quality, and in-depth risk management knowledge.
• Experience in design of user requirement specifications, IQ/OQ/PQ protocols, UAT and other qualification documentation.
• Fluent in standard Microsoft Office; experience with Maximo and quality systems software.

Responsibilities

• Provide QA Engineering support for Site Technology Transfer activities.
• Review validation/qualification documents for equipment, utilities and facilities.
• Review technology transfer documents and investigations with CAPA when needed.
• Ensure data governance and data integrity across site operations.
• Coach and develop direct reports if acting as people manager.

Skills

GMP knowledge

Risk management

IQ/OQ/PQ protocols

Maximo CMMS

Data integrity

Technical writing

Cross-functional collaboration

Quality systems

Tools

BMSDocs EDMS

Infinity/Valgenesis

Microsoft Office

Job description

Bristol Myers Squibb is seeking a Manager, QA Engineering (Equipment/Lab Methods/Utilities/Facilities) to oversee site technology transfer activities in a fast-paced manufacturing facility producing CAR T and drugs.

The role covers review of validation/qualification docs, change controls, and investigations with CAPA. It may be individual contributor or people manager, guiding cross-functional teams and ensuring data integrity per global standards.