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Project Engineer

応募後で応募 求人ID R0050615 掲載日 10/22/2021 Location:Dublin, Ireland

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Job Description


The Project Engineer reporting to the Project Engineering Manager is responsible for:

  • The implementation of engineering projects through full life cycle in compliance HPRA and FDA standards.
  • Managing 3rd party contractors in the execution of capital projects.
  • Ownership of budget and schedule for capital projects.
  • Liaise with 3rd party engineering companies to ensure delivery of capital projects.


  • Design, execute and manage engineering projects for the site, following Engineering Department standards.
  • Maintain strict budgetary control, while adhering to agreed schedules.
  • Contribute to the preparation of the site capital budget and support other Departments in securing capital funding for projects throughout the year.
  • Work collaboratively with other site teams in development and execution of projects.
  • Support technology transfer initiatives for incoming new products. This requires good communication and close cooperation with key Technology Transfer personnel from other departments.
  • Implement continuous improvement projects to improve availability and plant efficiency.
  • Initiate and complete validation documentation and testing as required.
  • Adhere to safe working practices as set out in the safety statement and other company safety rules.
  • Control and monitor safe working practices of contractors on site.
  • Actively encourage the culture of teamwork and integration within the Engineering Department and with all other Departments.


  • Participate fully in any cross functional training initiatives.
  • Drive and promote the corporate values of Takeda-ism within the workplace.
  • Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
  • Participate in safety and environmental initiatives.
  • Ensure timely completion of all SOP, reading, training and assessments.
  • Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.


The ideal candidate will have:

  • A 3rd level degree in Engineering, or equivalent, required.
  • Project Management accreditation would be an advantage.


  • At least 5 years’ experience in pharmaceutical project / Program management including experience in aseptic manufacturing environment.
  • Project management experience in biopharmaceutical operations involving cell cultures or Regenerative Medicines / ATMPs an advantage.
  • Excellent project management skills, Project Management Professional (PMP) or equivalent PM qualification is a plus.
  • Ability to plan workload and work to tight timelines.
  • Ability to communicate with site management, production, and quality personnel.
  • Good understanding of best practice safety procedures and standards applicable to construction and installation work.
  • Ability to produce technical documentation to a high standard.
  • Takes further responsibility/accountability for the management and execution of trouble shooting and projects in their specific area.
  • Excellent at knowledge sharing through mentoring and training to lift the average expertise level across the site in their area.


  • Safety focused.
  • A positive mindset and willingness to work with others.
  • The ability to work in a highly regulated industry and strive for continuous improvement.
  • Excellent interpersonal and communication skills.  
  • Ability to produce technical reports.
  • Strong Quality orientation.
  • Well organised and adaptable to change.
  • Ability to work on own initiative.
  • MS Project experience or equivalent.



Grange Castle, Ireland

Worker Type


Worker Sub-Type


Time Type

Full time