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About the Role

The Senior Manager of Global Reliability Engineering will support the roll out of global standards and drive reliability process improvements. This role will support talent/skills development, CMMS, and critical spares management for broader implementation.

Responsibilities

• Creating and rolling out global reliability processes, standards and best practices as part of the global Reliability Team
• Assist sites in the completion of reliability assessments, development of key metrics, and identification of reliability projects with most significant payback and bottom line impact to critical work center uptime.
• Develop reliability tools, standards and training materials for a broad range of reliability and maintenance topics (RCFA, Critical Spares Maintenance, RCM studies for PM Optimization etc.)
• Perform mechanical and electrical skills assessments across the network to baseline current maintenance and operations staff capabilities and assist 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, where possible, to improve site/asset reliability.
• Support/own critical asset replacement program (currently under responsibility of capital governance)
• Assists with periodic program and system / equipment audits focused on maintenance effectiveness, planning and scheduling and criticality assessments to rank assets according to business impact either financial or safety.
• Performs related duties as assigned.

Requirements

• Bachelor's degree in Chemical, Mechanical or Electrical Engineering or related discipline or 10+ years of reliability engineering support required.
• 7+ years of experience in pharmaceutical manufacturing facility/company required.
• 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.)
• Lean Six Sigma Experience
• Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
• 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.

Skills

• Reliability Centered Maintenance (RCM, RCM II, FMEA, Weibull Analysis)
• Lean Six Sigma
• Current Good Manufacturing Practices (cGMP)
• Food and Drug Administration (FDA)
• Predictive maintenance technologies (vibration, infrared, oil analysis, ultrasonic analysis)
• AI implementation for reliability
• CMMS
• Critical spares management

Location

• US Catalent site
• St Pete
• Kansas City
• Winchester
• Madison

Work Type

• Onsite
• Domestic travel (25%)
• Minimal international travel

Experience Level

• Senior Manager
• 7+ years of experience in pharmaceutical manufacturing facility/company
• 10+ years of hands on reliability engineering experience in a multi-site environment

Education Level

• Bachelor's degree in Chemical, Mechanical or Electrical Engineering or related discipline
• Advanced Degree in technical / business area a plus

Benefits

• Several Employee Resource Groups focusing on D&I
• Tuition Reimbursement
• Generous 401K match
• 152 hours accrued PTO + 8 paid holidays

About the Company

• Catalent is a leading global CDMO, trusted by pharma, biotech and self-care companies to accelerate the development, manufacturing and delivery of products that improve lives.
• With advanced technologies, deep expertise and a worldwide network, we partner with innovators to transform bold ideas into life-changing therapies and self-care solutions.
• Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
• Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
• Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives.
• Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply.
• With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year.
• Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

Equal Opportunity

• Catalent is an Equal Opportunity Employer, including disability and veterans.
• If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com.