Process Engineer
AbbVie
Process Engineer
Job Description
AbbVie are seeking a Process Engineer to join our engineering team in Westport, Co. Mayo. This is an exciting time to join our team as we bring new products and technologies to the site. The position is a 12 month fixed term contract and reports to the Associate Director, B1 Maintenance. The Process Engineer is responsible for providing technical assistance for equipment/machinery and all aspects of performance around the production and packaging of AbbVie products to meet customer requirements, FDA, HPRA, EPA and safety standards.Roles and ResponsibilitiesAssist with management, engineering, process improvement, equipment reliability, and control system activities.Identify, plan, schedule, manage and communicate on production related projects to all affected stakeholders.Ensuring systems, equipment, and products operate at optimal levels and meet Business Unit (BU) needs by preventing failures and maximizing uptimeAnalyse equipment failure data, conduct root cause analysis, develop and implement new procedures and processes to prevent reoccurrenceImplement lean technologies such as standard work, visualisation boards.Support the BU by developing robust process and systems to ensure delivery of effective quality.Ensure that line processes, equipment and materials are maintained to deliver consistent, reliable and predictable process performance and product quality.Develop & implement systems & structure to minimise technical downtime on the line.Resolve technical issues in an effective & timely manner with the technical team to support operations.Drive continuous improvement and process efficiency programs, i.e., OEE, OPEX, RCA, RCM and productivity output for the BU.Manage external vendors and services for equipment and technology in the BU along with Manufacturing.Manage technical documentation, reports, files, logs and records for the BU.Assist with the trending, monitoring, performance of equipment and the reduction of unplanned downtime.Help manage, track and monitor the relevant KPIs for the Technical Team.Assist with the trending, monitoring and reduction of repeat deviations associated with the equipment and technology in the BU. Generate and approve associated change controls and relevant protocols.Help support the BU during regulatory and compliance audits.
Locations
- Westport, MO
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
50,000 - 80,000 USD / yearly
Source: AI estimated from job description
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Process engineering and improvementintermediate
- Root cause analysis (RCA)intermediate
- Equipment reliability and maintenanceintermediate
- Lean technologies implementationintermediate
- Project management and stakeholder communicationintermediate
- Regulatory compliance (FDA, HPRA, EPA)intermediate
- Data analysis and KPI monitoringintermediate
- Vendor managementintermediate
- Technical documentation and change controlintermediate
Required Qualifications
- Degree in Engineering or related field (implied by role requirements) (experience)
- Experience in process engineering, equipment maintenance, and regulatory compliance in pharmaceutical manufacturing (experience)
Responsibilities
- Assist with management, engineering, process improvement, equipment reliability, and control system activities
- Identify, plan, schedule, manage and communicate on production related projects to all affected stakeholders
- Ensuring systems, equipment, and products operate at optimal levels and meet Business Unit (BU) needs by preventing failures and maximizing uptime
- Analyse equipment failure data, conduct root cause analysis, develop and implement new procedures and processes to prevent reoccurrence
- Implement lean technologies such as standard work, visualisation boards
- Support the BU by developing robust process and systems to ensure delivery of effective quality
- Ensure that line processes, equipment and materials are maintained to deliver consistent, reliable and predictable process performance and product quality
- Develop & implement systems & structure to minimise technical downtime on the line
- Resolve technical issues in an effective & timely manner with the technical team to support operations
- Drive continuous improvement and process efficiency programs, i.e., OEE, OPEX, RCA, RCM and productivity output for the BU
- Manage external vendors and services for equipment and technology in the BU along with Manufacturing
- Manage technical documentation, reports, files, logs and records for the BU
- Assist with the trending, monitoring, performance of equipment and the reduction of unplanned downtime
- Help manage, track and monitor the relevant KPIs for the Technical Team
- Assist with the trending, monitoring and reduction of repeat deviations associated with the equipment and technology in the BU. Generate and approve associated change controls and relevant protocols
- Help support the BU during regulatory and compliance audits
Benefits
- general: 12-month fixed term contract with opportunity to work on new products and technologies
- general: Position within a leading pharmaceutical company (AbbVie) in Westport, Co. Mayo
Tags & Categories
Process Engineer
AbbVie
Process Engineer
Job Description
AbbVie are seeking a Process Engineer to join our engineering team in Westport, Co. Mayo. This is an exciting time to join our team as we bring new products and technologies to the site. The position is a 12 month fixed term contract and reports to the Associate Director, B1 Maintenance. The Process Engineer is responsible for providing technical assistance for equipment/machinery and all aspects of performance around the production and packaging of AbbVie products to meet customer requirements, FDA, HPRA, EPA and safety standards.Roles and ResponsibilitiesAssist with management, engineering, process improvement, equipment reliability, and control system activities.Identify, plan, schedule, manage and communicate on production related projects to all affected stakeholders.Ensuring systems, equipment, and products operate at optimal levels and meet Business Unit (BU) needs by preventing failures and maximizing uptimeAnalyse equipment failure data, conduct root cause analysis, develop and implement new procedures and processes to prevent reoccurrenceImplement lean technologies such as standard work, visualisation boards.Support the BU by developing robust process and systems to ensure delivery of effective quality.Ensure that line processes, equipment and materials are maintained to deliver consistent, reliable and predictable process performance and product quality.Develop & implement systems & structure to minimise technical downtime on the line.Resolve technical issues in an effective & timely manner with the technical team to support operations.Drive continuous improvement and process efficiency programs, i.e., OEE, OPEX, RCA, RCM and productivity output for the BU.Manage external vendors and services for equipment and technology in the BU along with Manufacturing.Manage technical documentation, reports, files, logs and records for the BU.Assist with the trending, monitoring, performance of equipment and the reduction of unplanned downtime.Help manage, track and monitor the relevant KPIs for the Technical Team.Assist with the trending, monitoring and reduction of repeat deviations associated with the equipment and technology in the BU. Generate and approve associated change controls and relevant protocols.Help support the BU during regulatory and compliance audits.
Locations
- Westport, MO
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
50,000 - 80,000 USD / yearly
Source: AI estimated from job description
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Process engineering and improvementintermediate
- Root cause analysis (RCA)intermediate
- Equipment reliability and maintenanceintermediate
- Lean technologies implementationintermediate
- Project management and stakeholder communicationintermediate
- Regulatory compliance (FDA, HPRA, EPA)intermediate
- Data analysis and KPI monitoringintermediate
- Vendor managementintermediate
- Technical documentation and change controlintermediate
Required Qualifications
- Degree in Engineering or related field (implied by role requirements) (experience)
- Experience in process engineering, equipment maintenance, and regulatory compliance in pharmaceutical manufacturing (experience)
Responsibilities
- Assist with management, engineering, process improvement, equipment reliability, and control system activities
- Identify, plan, schedule, manage and communicate on production related projects to all affected stakeholders
- Ensuring systems, equipment, and products operate at optimal levels and meet Business Unit (BU) needs by preventing failures and maximizing uptime
- Analyse equipment failure data, conduct root cause analysis, develop and implement new procedures and processes to prevent reoccurrence
- Implement lean technologies such as standard work, visualisation boards
- Support the BU by developing robust process and systems to ensure delivery of effective quality
- Ensure that line processes, equipment and materials are maintained to deliver consistent, reliable and predictable process performance and product quality
- Develop & implement systems & structure to minimise technical downtime on the line
- Resolve technical issues in an effective & timely manner with the technical team to support operations
- Drive continuous improvement and process efficiency programs, i.e., OEE, OPEX, RCA, RCM and productivity output for the BU
- Manage external vendors and services for equipment and technology in the BU along with Manufacturing
- Manage technical documentation, reports, files, logs and records for the BU
- Assist with the trending, monitoring, performance of equipment and the reduction of unplanned downtime
- Help manage, track and monitor the relevant KPIs for the Technical Team
- Assist with the trending, monitoring and reduction of repeat deviations associated with the equipment and technology in the BU. Generate and approve associated change controls and relevant protocols
- Help support the BU during regulatory and compliance audits
Benefits
- general: 12-month fixed term contract with opportunity to work on new products and technologies
- general: Position within a leading pharmaceutical company (AbbVie) in Westport, Co. Mayo
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