close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to applications@lifescience.ie
Details

Senior Equipment Design Engineer


Reference:Dublin - Senior Equipment Engineer Location: Dublin
Dublin City Centre
Dublin Greater
Dublin North
Dublin South
Dublin West
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed

Company:
My client are a Pharma and Medical Device company developing combination products who have a global portfolio which includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas.
They are committed to helping create healthier communities worldwide through education, outreach and better access to treatment


Role:Senior Equipment Design Engineer
Location:Newenham Court, Northern Cross, Malahide rd, Dublin 17
Benefits:Competitive salary, bonus, pension and full family healthcare


Overview:
The Senior Device Equipment Engineer will be an SME in the management and delivery of equipment, inclusive of specification, procurement, delivery, qualification, and project management of the same.

You will lead equipment delivery projects with the suppliers, inclusive of budget management, and ownership for specification and qualification. Also work in collaboration with cross organisational teams; R&D, CMO, ensuring delivery to specification and local site requirements.

This is a Global role that is key to the success of GDD’s varied product portfolio delivery and will provide the successful candidate exposure to all aspects of combination device design, development, and production.



Day to day:

  • Project owner from conception to realisation. Develop engineering systems strategy for program delivery. Pilot to scale up, subassembly, final assembly, transport, and auxiliary systems, establishing and maintaining timelines against organisation requirements and identify external partners to meet internal needs.
  • Lead for engineering systems in cross departmental teams. Manage engineering system objectives in line with program delivery. Supporting the device program team through communication, plan management, technical review and execution, budgetary management, risk assessment, etc.
  • Point of contact and relationship owner for external partners. Responsible for alignment of cross organisation requirement to GDD specification and needs. First point of contact for escalations, and alignment of external deliveries to internal plans.
  • Accurately plan and manage budgetary needs to support program delivery, capital request development and approval, business justification and contract management. Supporting engineering systems with accurate reporting and supporting program management and finance metrics.
  • Management of budgets associated with external suppliers, ensuring proactive budget forecasting, invoicing management at qualification phases and where appropriate cost reduction programs.



Experience required:
  • Degree in Science/Engineering with 5+ years’ experience in pharmaceutical and/or medical device development or similar role.
  • Strong project management experience is highly preferred.
  • Enthusiastic, conscientious, highly driven and motivated person.
  • Good communication skills and commitment to teamwork are essential.
  • Writing technical reports and producing high quality documentation within a regulatory controlled GMP environment



Does this sound like your next career move? For more info forward your application or contact me on 087 0612325 ORthomas.gallagher@lifescience.ie




Life Science Production Engineer Upstream Process Regulatory Affairs Consultant Validation Specialist QA Engineer Research Assistant Academic North Leinster Senior Manufacturing Engineer Engineering Manager Senior Automation Engineer Senior Project Manager R and D Director Principal Engineer QA RA Engineer QA Supervisor Principal Research Scientist IT Professional Medical Device Technical Support Specialist Design Engineer Process Technician Galway City Louth Quality Systems Lead Electronic Engineer QA Specialist Regulatory Affairs Officer Manufacturing Coordinator Contract Automation Engineer Technical Specialist Meath Supply Chain Quality Specialist Project Engineer Cavan Senior Test Engineer Chemistry Research and Development Technician QA Executive QA Validation Specialist Programmer R & D Technician Research Engineer Validation Scientist Republic of Ireland Quality Assurance Technologist Manufacturing Engineer QE Manufacturing Engineer Manufacturing and Technology Manager Senior Quality Engineer Healthcare Limerick City Quality Control Manager Quality Systems Administator Regulatory Affairs Specialist NPD Technologist Research Fellow Maintenance Technician Product Specialist Connaught Senior Research and Development Engineer Longford Snr R and D Engineer Maintenance Engineer Kilkenny Regulatory Affairs Supplier Quality Engineer Microbiology Hardware Implementation Engineer Biomedical Scientist Research and Development Engineer Biotechnologist Design Assurance Bioprocess Engineer Quality Assurance Junior Product Specialist Validation Manager Process Development Engineer QA Director Roscommon Validation Engineer Athlone Research Scientist Dublin South Biopharmaceutical EHS Engineer Research and Development Scientific Process Engineer Leitrim Business Development Executive BD Manager Offaly Principal Scientist Clare Senior Research and Development Scientist Dublin City Centre IT Solutions Quality Manager Regulatory Affairs Executive Equipment Engineer Engineering Software Engineer Biotechnician Consultant (Medical) Kildare Research and Development Scientist Connected Health New Product Development Engineer Regulatory Affairs Director Product Development Engineer Regulatory Affairs Quality Engineer QA Manager Medical Affairs R and D Manager Mechanical Engineer R and D Biochemist Quality Systems Engineer Clinical Project Manager Supply Chain Applications Engineer Snr Validation Engineer Quality Control Supervisor Regulatory Affairs Manager Project Development Engineer Product Development Technologist Mayo Dublin West Electrical Engineer Galway Pharmaceutical Senior Operations Engineer Life Science C++ Software Engineer Limerick Project Manager Engineering Academic Donegal Manufacturing Executive Regulatory Affairs Clinical Research Dublin Senior Project Engineer Sligo Clinical Research Product Manager Software Developer Leinster Westmeath Technical Project Manager Project Lead Biotechnology Specialist Quality Systems Specialist Biotechnology Contract Lead Quality Engineer Dublin Greater Biomedical Engineer Midlands Senior Regulatory Affairs Officer Technical Support Laois Dublin North Operational Excellence Lead Graduate