Sr Automation Engineer Technical Team Lead - Ft Contract jobs at West Pharma in Ireland, Dublin

Note: This is a 12-month fixed term contract.

In this role, you will be responsible for developing new technology and supporting existing technology to improve production, quality, profitability and safety. This individual will be responsible for the planning, scheduling, execution of projects and communicating project status to targeted timelines. This individual will also manage/assist in facility expansion/modifications.

• Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety.
• Develop, execute and document project assignments in compliance with committed timelines and project goals, and per established governance policies and procedures.
• Ensure technical and customer requirements for assigned projects are achieved.
• Develop and maintain required validation and project management documents.
• Conduct or participate in routine project reviews with Project Teams and Management
• Perform design work, layouts, sketches, concepts, etc. as needed for projects and/or plant layouts.
• Develop and/or review engineering change requests for modifications to processes, equipment and facilities.
• Troubleshoot and repair of all automation.
• Evaluate and maintain proper machine safeties to ensure employees are protected when operating any piece of automation.
• Ensure automation lines are meeting their targeted output and OEE by analyzing production data.
• Maintain quality finished product through proper maintenance and operation of all automation.
• Provide timely notification to shift leaders and program managers of maintenance and down time issues.
• Interfaces daily with engineering manager and shift support staff.
• Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
• Performs other duties as assigned by management.
• Exhibits regular, reliable, punctual and predictable attendance.
• Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management.

• Associate's Degree In a relevant Engineering subject required or
• Bachelor's Degree In a relevant Engineering subject preferred

• Minimum 3 years Experience in medical device industry or other regulated industry required
• Minimum 3 years Experience in supporting technical project management preferred

• Background in medical devices/pharmaceutical would be a plus.
• Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards

• Must be able to work a 40-hour work week, plus overtime and/or irregular hours as required to complete assignments. May stand or sit for extended periods of time. Must transport oneself to and from other areas of the facility and travel to other divisions when necessary. Must have good visual acuity. If specifically necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues.
• Medical Device manufacturing requires strict adherence to standards. Working environment is a manufacturing facility, which houses plastic injection molding machines. Must tolerate fumes and particulate generated from various plastics. Work areas are equipped with adequate lighting, cooling/heating and equipment that are in a good working condition. Must work constructively in an environment that may always be stressful due to competing resources while maintaining company confidentiality.

Note: This is a 12-month fixed term contract.

In this role, you will be responsible for developing new technology and supporting existing technology to improve production, quality, profitability and safety. This individual will be responsible for the planning, scheduling, execution of projects and communicating project status to targeted timelines. This individual will also manage/assist in facility expansion/modifications.

• Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety.
• Develop, execute and document project assignments in compliance with committed timelines and project goals, and per established governance policies and procedures.
• Ensure technical and customer requirements for assigned projects are achieved.
• Develop and maintain required validation and project management documents.
• Conduct or participate in routine project reviews with Project Teams and Management
• Perform design work, layouts, sketches, concepts, etc. as needed for projects and/or plant layouts.
• Develop and/or review engineering change requests for modifications to processes, equipment and facilities.
• Troubleshoot and repair of all automation.
• Evaluate and maintain proper machine safeties to ensure employees are protected when operating any piece of automation.
• Ensure automation lines are meeting their targeted output and OEE by analyzing production data.
• Maintain quality finished product through proper maintenance and operation of all automation.
• Provide timely notification to shift leaders and program managers of maintenance and down time issues.
• Interfaces daily with engineering manager and shift support staff.
• Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
• Performs other duties as assigned by management.
• Exhibits regular, reliable, punctual and predictable attendance.
• Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management.

• Associate's Degree In a relevant Engineering subject required or
• Bachelor's Degree In a relevant Engineering subject preferred

• Minimum 3 years Experience in medical device industry or other regulated industry required
• Minimum 3 years Experience in supporting technical project management preferred

• Background in medical devices/pharmaceutical would be a plus.
• Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards

• Must be able to work a 40-hour work week, plus overtime and/or irregular hours as required to complete assignments. May stand or sit for extended periods of time. Must transport oneself to and from other areas of the facility and travel to other divisions when necessary. Must have good visual acuity. If specifically necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues.
• Medical Device manufacturing requires strict adherence to standards. Working environment is a manufacturing facility, which houses plastic injection molding machines. Must tolerate fumes and particulate generated from various plastics. Work areas are equipped with adequate lighting, cooling/heating and equipment that are in a good working condition. Must work constructively in an environment that may always be stressful due to competing resources while maintaining company confidentiality.

Note: This is a
12 month fixed term contract.

In this role, you will be responsible for developing new technology and supporting existing technology to improve production, quality, profitability and safety. This individual will be responsible for the planning, scheduling, execution of projects and communicating project status to targeted timelines. This individual will also manage/assist in facility expansion/modifications.

• Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety.
• Develop, execute and document project assignments in compliance with committed timelines and project goals, and per established governance policies and procedures.
• Ensure technical and customer requirements for assigned projects are achieved.
• Develop and maintain required validation and project management documents.
• Conduct or participate in routine project reviews with Project Teams and Management
• Perform design work, layouts, sketches, concepts, etc. as needed for projects and/or plant layouts.
• Develop and/or review engineering change requests for modifications to processes, equipment and facilities.
• Troubleshoot and repair of all automation.
• Evaluate and maintain proper machine safeties to ensure employees are protected when operating any piece of automation.
• Ensure automation lines are meeting their targeted output and OEE by analyzing production data.
• Maintain quality finished product through proper maintenance and operation of all automation.
• Provide timely notification to shift leaders and program managers of maintenance and down time issues.
• Interfaces daily with engineering manager and shift support staff.
• Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
• Performs other duties as assigned by management.
• Exhibits regular, reliable, punctual and predictable attendance.
• Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management.

• Associate's Degree In a relevant Engineering subject required or
• Bachelor's Degree In a relevant Engineering subject preferred

• Minimum 3 years Experience in medical device industry or other regulated industry required
• Minimum 3 years Experience in supporting technical project management preferred

• Background in medical devices/pharmaceutical would be a plus.
• Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards

• Must be able to work a 40-hour work week, plus overtime and/or irregular hours as required to complete assignments. May stand or sit for extended periods of time. Must transport oneself to and from other areas of the facility and travel to other divisions when necessary. Must have good visual acuity. If specifically necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues.
• Medical Device manufacturing requires strict adherence to standards. Working environment is a manufacturing facility, which houses plastic injection molding machines. Must tolerate fumes and particulate generated from various plastics. Work areas are equipped with adequate lighting, cooling/heating and equipment that are in a good working condition. Must work constructively in an environment that may always be stressful due to competing resources while maintaining company confidentiality.

Note: This is a Fixed-Term contract until June 2026

Reporting to the Toolroom Supervisor, the Toolmaker will be responsible for the maintenance and repair of all moulds in operation at West. This role involves working closely with Toolroom Leads and Production Group Leaders to understand daily priorities and ensure resolution to tooling issues in a timely manner.

• Responsible for the repair and maintenance of moulds including investigations and root cause analysis of major tooling issues.
• Responsible for the manufacture of jigs & fixtures, in the support of mould and equipment maintenance.
• Gathers critical tooling information for report composition.
• Identifies continuous tooling improvements for future/repeat moulds.
• Reports/escalates all issues to Toolroom Supervisor.
• Assists the Toolroom Supervisor in the development of tooling documentation and the compiling of maintenance procedures for each mould.
• Works with Production Group Leaders in troubleshooting mould issues.
• Solves, in conjunction with the Quality Department, customer related issues as required.
• Attends internal meetings to establish priorities.
• Liaises with external suppliers on the repair/replacement of tooling components and equipment.
• Assists the Toolroom Supervisor in the identification and development of talent within the team and delivering training as required to new employees and apprentices.
• Responsible for the capture of all tooling intervention information and data on CMMS
• Proposes improvements to processes and procedures to Toolroom Lead and Supervisor
• Works autonomously within established procedures and practices
• Supports and contributes in Lean Sigma projects
• Complies to all site Environmental, Health and Safety requirements, training and regulations.
• Complies to all local site company policies, procedures and corporate policies.
• Acts in accordance with West’s Guiding Principles and adheres to the Corporate Code of Conduct
• Perform additional duties at the request of the direct supervisor.

• Toolmaking qualification

• Minimum 3 year’s experience ideally with time served producing injection moulds.
• Excellent machining knowledge and skills.
• Previous experience in a mould maintenance environment supporting high volume manufacturing.

• Strong written and verbal communication skills
• Good understanding of the injection moulding process
• Experience in maintaining hot runner systems
• Knowledge of CMMS.
• Ability to weld.
• Knowledge of tooling hydraulics, pneumatics and electrics
• Proficient IT skills, specifically Microsoft Office (Word, Excel, Powerpoint and Outlook)
• Experience in 3D modelling and drawing software packages (eg. Solidworks).

Physical:

• Job-related activities that require physical activity:
• Must be able to stand/walk for periods of up to 4 hours between rest periods.
• Must be able to lift equipment and tools up to 25kg up to 10 times per day.
• Must be able to climb up and down stepladders/stairs up to 10 times per day.

Mental:

• Ability to reason logically and make sound decisions, to consider alternative and diverse perspectives and to communicate effectively both orally and in writing
• Ability to simultaneously address multiple complex problems.
• Ability to work as an integral part of a team.
• Ability to work under pressure.
• Ability to understand, remember and follow verbal and written instructions.
• Ability to complete assigned tasks without direct supervision.

• Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety.
• Develop, execute and document project assignments in compliance with committed timelines and project goals, and per established governance policies and procedures.
• Ensure technical and customer requirements for assigned projects are achieved.
• Develop and maintain required validation and project management documents.
• Conduct or participate in routine project reviews with Project Teams and Management
• Perform design work, layouts, sketches, concepts, etc. as needed for projects and/or plant layouts.
• Develop and/or review engineering change requests for modifications to processes, equipment and facilities.
• Troubleshoot and repair of all automation.
• Evaluate and maintain proper machine safeties to ensure employees are protected when operating any piece of automation.
• Ensure automation lines are meeting their targeted output and OEE by analyzing production data.
• Maintain quality finished product through proper maintenance and operation of all automation.
• Provide timely notification to shift leaders and program managers of maintenance and down time issues.
• Interfaces daily with engineering manager and shift support staff.
• Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
• Performs other duties as assigned by management.
• Exhibits regular, reliable, punctual and predictable attendance.
• Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management.

• Associate's Degree In a relevant Engineering subject required or
• Bachelor's Degree In a relevant Engineering subject preferred

• Minimum 3 years Experience in medical device industry or other regulated industry required
• Minimum 3 years Experience in supporting technical project management preferred

• Background in medical devices/pharmaceutical would be a plus.
• Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards

• Must be able to work a 40-hour work week, plus overtime and/or irregular hours as required to complete assignments. May stand or sit for extended periods of time. Must transport oneself to and from other areas of the facility and travel to other divisions when necessary. Must have good visual acuity. If specifically necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues.
• Medical Device manufacturing requires strict adherence to standards. Working environment is a manufacturing facility, which houses plastic injection molding machines. Must tolerate fumes and particulate generated from various plastics. Work areas are equipped with adequate lighting, cooling/heating and equipment that are in a good working condition. Must work constructively in an environment that may always be stressful due to competing resources while maintaining company confidentiality.

NOTE: THIS IS A FIXED-TERM CONTRACT UNTIL 2026

Supports manufacturing projects and contributes to the development and implementation of the business manufacturing strategy. Responsible for the implementation of manufacturing solutions to meet the requirements of customers’ product introductions. Reports directly to the Senior Automation Engineer.

• Support equipment process and product introduction projects
• Work on the implementation of the manufacturing strategy to meet customer and Tech Group Europe needs.
• Participate in project teams, identifying deliverables, time and cost, setting priorities and reporting to meet the needs of the business and the customer.
• Supports Tech Group Europe’s relationships with the customers and equipment suppliers in pursuit of new business, product development, manufacturing process development, continuous improvement and on-going business development.
• Work with equipment suppliers ensuring delivery meets specification, cost and time.
• Ensure that equipment meets the regulatory requirements of the business. Validation, health and safety etc.
• Support the installation of equipment with appropriate training and hand over to operations
• Work with all departments across the business to ensure that processes meet their requirements.
• Identify, specify and introduce manufacturing methods and opportunities into the company
• Assist with the training and development of personnel in Tech Group Europe on processes or systems introduced to the company.
• Ensure that the procedures and systems are in place to facilitate the introduction of processes and equipment.
• Carry out maintenance of equipment where needed
• Act in accordance with the company’s Guiding Principles and adherence to the corporate Code of Conduct.
• Compliance to all site Environmental, Health and Safety requirements, training and regulations.
• Compliance to all local site company policies, procedures and corporate policies.
• Perform additional duties at the request of the direct supervisor.

• Minimum Level 6 in engineering discipline

• Minimum 2 years Experience in medical device industry or other regulated industry required
• Minimum 2 years Experience in supporting technical project management preferred

• Must have knowledge in computer systems, word processing and spreadsheets, and ideally in integrated manufacturing systems, Allen Bradley & Siemens PLC’s,Motion and Machine Control Systems.
• Must have knowledge of Robotics, Cognex Vision Systems, Barcode Scanning & RFID Automatic Identification and Data Capture used in High Volume Manufacturing.
• Preferably have a knowledge of Industrial Networks (Ethernet IP,Control Net & Profibus) and has worked on an MES system. Must have a good understanding of Manufacturing Automation, and ideally in Machine design, Development and Validation Process.
• Preferably worked in either the Medical, Packaging or technological industries with a good understanding of the regulatory requirements.
• Must have good written and verbal communication skills as well as the ability to accurately document work performed.
• Must be able to work in a fast paced environment.
• Must be able to travel as required by the position.
• Must be able to organize and prioritize tasks; must be detail orientated and self-motivated.
• Must be able to work independently on own projects while working concurrently with all departments and levels of employees.
• Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards

• This is a 4 cycle 24/7 shift role.

Note: This is a Fixed Term contract until June 2026

In this role, you will effectively plan and guide Engineering team, ensuring quality product and operational efficiencies are met.

• Mentor and may lead engineering team to achieve site and department goals in a fast-paced environment.
• Collaborate with cross-functional teams to develop and implement sustainable manufacturing processes and systems.
• Technical and hands-on automated equipment troubleshooting, repair, and improvements.
• Perform and document engineering studies and evaluations.
• Analyze data to drive improvements, determine prioritization, and identify opportunities.
• Lead and provide mentorship in root cause and corrective action (RCCA).
• Assess and perform/schedule technical training, including electromechanical systems, pneumatics, servos, PLCs, schematic reading/interpretation, new technology, etc.
• Champion high-visibility projects. Develop project scope, timeline, savings, and cost estimations.
• Quote new automation lines, engineering services, etc. Develop design concepts for new automation.
• Write validation, user requirements, equipment specification, and other documents as needed.
• Establishes relationships with customer and automation suppliers in pursuit of win?win results and ongoing business.
• Provide engineering assistance to assure plant, machinery, and processes are at an optimum level.
• Routinely evaluate and review employee performance.
• Promote and support a Lean Manufacturing environment within the facility.
• Research new technologies and methodologies to use in the plant.
• Provide a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
• Perform other duties as assigned based on business needs.
• Conform with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
• Exhibit regular, reliable, punctual and predictable attendance.
• Other duties as assigned.

• Bachelor's Degree In Engineering or Science field required
• Master's Degree In Engineering or Science field preferred

• Minimum 5 years 5-8 years of experience required and
• 2+ years of managerial or supervisory experience in manufacturing environment required and
• Strong automation background and experience with CAD and SAP systems a plus. preferred

• Knowledge of manufacturing processes, workflows, production equipment and industrial techniques.
• Must have effective problem solving and interpersonal skills.

• Manufacturing\Six Sigma Green Belt Certification Six Sigma green belt Upon Hire preferred or
• Manufacturing\Lean Six Sigma Black Belt Six Sigma black belt Upon Hire preferred

• Must be able to perform job duties as required with limited physical demands.