Sr. Manager of Global Reliability Engineering

About the role

The Senior Manager of Global Reliability Engineering supports the roll out of global standards and drives reliability process improvements. This role assists sites in reliability assessments, develops reliability tools, standards, and training materials, performs mechanical and electrical skills assessments, and implements predictive maintenance technologies.

Responsibilities

• Create and implement global reliability processes, standards, and best practices.
• Support sites in reliability assessments, development of key metrics, and identification of reliability projects.
• Develop reliability tools, standards, and training materials for a broad range of reliability and maintenance topics.
• Perform mechanical and electrical skills assessments to baseline current maintenance and operations staff capabilities.
• Aid sites in developing training plans to improve skills in maintenance, equipment setup, and troubleshooting.
• Support the rollout of predictive maintenance technologies such as vibration, infrared, oil analysis, ultrasonic analysis, and other non-destructive technologies.
• Implement use of AI to improve site/asset reliability.
• Support/own critical asset replacement program.
• Assist with periodic program and system/equipment audits focused on maintenance effectiveness, planning, and scheduling.
• Perform related duties as assigned.

Requirements

• Bachelor's degree in Chemical, Mechanical, or Electrical Engineering or related discipline or 10+ years of reliability engineering support.
• Advanced Degree in technical/business area a plus.
• 7+ years of experience in pharmaceutical manufacturing facility/company.
• 10+ years of hands-on reliability engineering experience in a multi-site environment.
• Formal Training in Reliability Centered Maintenance methodologies (RCM, RCM II, FMEA, Weibull Analysis etc.).
• Leverage Lean Six Sigma Experience.
• Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
• Experience with pharmaceutical/bio tech processing equipment is a plus.
• Communicating clearly and concisely, both orally and in writing.
• Remaining current in all aspects of cGMPs and SOPs, methods, and protocols.
• Fluent in English written and verbal conversational and technical.
• 25% domestic travel, minimal international travel.

Qualifications

• Personal initiative.
• Dynamic pace.
• Meaningful work.

Benefits

• Several Employee Resource Groups focusing on D&I.
• Tuition Reimbursement – Let us help you finish your degree or earn a new one!
• Generous 401K match.
• 152 hours accrued PTO + 8 paid holidays.

Pay

Compensation is commensurate with experience.

Schedule

Typical working hours are Monday-Friday 8 AM-5 PM. When not traveling, the position requires being onsite at a US Catalent site.