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 R&D Manager


Reference:TG - R&D Manager - Galway Location: Athlone
Clare
Connaught
Galway
Galway City
Leitrim
Limerick
Limerick City
Qualification:DegreeExperience:10+ Years
Job Type:PermanentSalary: Not Disclosed

Job title:Senior R&D Manager
Location:Ballybrit, Galway
Benefits:Excellent salary, bonus, pension, healthcare and opportunity to grow your career with hugely exciting Medical Device organisation.

Company:
My client are a Medical Device company who have recently been acquired by a multinational, a global leader in neurovascular care. And a broad portfolio of devices used in the endovascular treatment of haemorrhagic and ischemic stroke.My client invests in their people, and take great pride in providing a positive work environment which respects diversity, supports wellbeing, and embraces innovation.


About the role:
As a Senior R&D Manager in the lifecycle Management department will provide leadership to a growing R&D LCM team, technologies, and overarching program management of R&D departmental deliverables. The portfolio of products under R&D LCM ownership is increasing significantly in 2024, so we are looking for a new leader shape the LCM function of the R&D department. This is a fantastic and rare opportunity if you desire to “put your stamp” on something that will have a legacy impact on the organisation.




Some responsibilities include:

  • Responsible for R&D Lifecycle Management (LCM) activities for the portfolio of products.
  • R&D LCM team leadership, with responsibly for team structure, team development, and performance management.
  • Manage interfaces between other functions, especially Supply Chain, Quality and Regulatory, to plan and support R&D activities required to support product lifecycle management.
  • Organizing and prioritizing activities, including escalations, in collaboration with key functions and aligning on deliverables and timing.
  • Utilizing the strengths of your team and providing direct leadership, be the source of technical expertise of a broad range of neurovascular ischemic and haemorrhagic stroke products.
  • Work closely and deliver on tasks/projects with cross functional teams including:
  • Quality and Design Assurance in risk identification and assessment of any design and process changes, R&D representative for re-certification and vendor audits.
  • Supply Chain and Manufacturing in developing and implementing cost improvement programs with external manufacturing partners.
  • Liaising with Regulatory team to develop approaches to gain approval of portfolio products in additional regions which may require bespoke R&D test programs.
  • Marketing teams to aid with product promotional activities at scientific conferences and deliver on competitive testing claims needs.
  • Support R&D department with customer (physician) visitors in terms of presenting on the development history of our product portfolio.
  • Leading customer complaint technical investigations and site representative for review meetings. R&D point-person to review complaint trending, alert and action levels.

    Requirements:

  • Honours degree in Engineering or Science (desired) with strong technical acumen,
  • Professional certification in Project Management (PMP) preferred.
  • Significant experience in an R&D or product sustaining role in the medical device industry.
  • Team leadership experience required.
  • Proficiency in statistical techniques.
  • Ability to work within design control systems and processes




What awaits you:


This is an opportunity to work with a ground-breaking biomedical operation, part of a company with an excellent record in employee continuous professional development and business improvement.


- An opportunity to be part of a global market leader.


- A dynamic and inspiring working environment.


- Opportunities to work on challenging projects and assignments.


- Possibilities for further personal and professional development/education.


- Excellent benefits




Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on 087 0612325 OR thomas.gallagher@lifescience.ie




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