Maintenance Engineer, Sterile Drug Product Maintenance
Bristol Myers Squibb
50% onsite
Level 8 engineering qualification or equivalent
3 years experience in regulated manufacturing
Experience with maximo or equivalent cmms system
The role involves supporting the facility during project phases, including equipment installation, commissioning, and transition to operational phases for sterile drug product commercialization
Job Summary
The role involves supporting the facility during project phases, including equipment installation, commissioning, and transition to operational phases for sterile drug product commercialization.
Engineers are responsible for developing Standard Operating Procedures, creating preventive maintenance routines, and ensuring compliance with GMP, safety, and environmental requirements.
Bristol Myers Squibb offers a competitive benefits package and emphasizes a culture of balance, flexibility, and life-changing work that transforms patient lives.
Matching Summary
The role involves supporting the facility during project phases, including equipment installation, commissioning, and transition to operational phases for sterile drug product commercialization.
Skills & Requirements
Must-have
Level 8 Engineering qualification or equivalent
3 years experience in regulated manufacturing
Experience with Maximo or equivalent CMMS system
Knowledge of GMP and safety regulations
Root cause analysis and failure investigation
Nice-to-have
Experience with site start-up and handover
Background in Sterile Fill Finish operations
Proficiency in data visualization tools like Spotfire
Ability to work independently and remotely
Strong communication and cross-functional collaboration