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דרושים Analista De Projetos Pleno ב-West Pharma ב-Ireland, Dublin

מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Analista De Projetos Pleno ב-Ireland, Dublin והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו West Pharma. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
חברה (1)
אופי המשרה
קטגוריות תפקיד
שם תפקיד (1)
Ireland
Dublin
נמצאו 2 משרות
21.11.2025
WP

West Pharma Analista Sr de RH Adm Pessoal e Benefícios Ireland, Dublin

Limitless High-tech career opportunities - Expoint
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...
תיאור:

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.

Essential Duties and Responsibilities
  • 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.
Education
  • Associate's Degree In a relevant Engineering subject required or
  • Bachelor's Degree In a relevant Engineering subject preferred
Work Experience
  • Minimum 3 years Experience in medical device industry or other regulated industry required
  • Minimum 3 years Experience in supporting technical project management preferred
Preferred Knowledge, Skills and Abilities
  • Background in medical devices/pharmaceutical would be a plus.
  • Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards
Physical Requirements
Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.
Additional Requirements
  • 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.
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06.07.2025
WP

West Pharma Analista de Projetos Pleno Ireland, Dublin

Limitless High-tech career opportunities - Expoint
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...
תיאור:
Job Summary

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.

Essential Duties and Responsibilities
  • 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.
Education
  • Toolmaking qualification
Work Experience
  • 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.
Preferred Knowledge, Skills and Abilities
  • 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 Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Physical and Mental Requirements

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.
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משרות נוספות שיכולות לעניין אותך

Limitless High-tech career opportunities - Expoint
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...
תיאור:

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.

Essential Duties and Responsibilities
  • 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.
Education
  • Associate's Degree In a relevant Engineering subject required or
  • Bachelor's Degree In a relevant Engineering subject preferred
Work Experience
  • Minimum 3 years Experience in medical device industry or other regulated industry required
  • Minimum 3 years Experience in supporting technical project management preferred
Preferred Knowledge, Skills and Abilities
  • Background in medical devices/pharmaceutical would be a plus.
  • Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards
Physical Requirements
Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.
Additional Requirements
  • 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.
Show more
בואו למצוא את עבודת החלומות שלכם בהייטק עם אקספוינט. באמצעות הפלטפורמה שלנו תוכל לחפש בקלות הזדמנויות Analista De Projetos Pleno בחברת West Pharma ב-Ireland, Dublin. בין אם אתם מחפשים אתגר חדש ובין אם אתם רוצים לעבוד עם ארגון ספציפי בתפקיד מסוים, Expoint מקלה על מציאת התאמת העבודה המושלמת עבורכם. התחברו לחברות מובילות באזור שלכם עוד היום וקדמו את קריירת ההייטק שלכם! הירשמו היום ועשו את הצעד הבא במסע הקריירה שלכם בעזרת אקספוינט.