I'm looking for...
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
Research Assistant
Cork City
EDW Architect
Dublin
Microbiologist
Republic of Ireland
QA Engineer
Galway
Senior CRA
Dublin
Qualified Person
East Midlands
QC Supervisor
Dublin
QC Chemist
Dublin
QC Analyst
Cork
QA RA Engineer
Roscommon
QC Analyst
Waterford
Senior RF Analog Engineer
Republic of Ireland
Senior Pharmacoviligance Officer
Republic of Ireland
DIS Programmer
England
EU BD Manager
Offaly
QA Auditor
Dublin


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 and D Engineer


Reference:JCHQ00000340 Location: Westmeath
Qualification:DegreeExperience:7-9 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: R and D Manager

Senior R and D Engineer
Our client a multinational medical device company currently seeks a senior R&D Engineer to join their team. Successful candidate will be responsible for the design and development of new technologies and/or products. Will provide design expertise to R&D, manufacturing and product quality.


Role/Responsibilities



  • Responsible for the design and development of creative and innovative, mechanical, electrical or chemical solutions which lead to the development and introduction of new technologies, products and/or processes that support ongoing business objectives.

  • Using Solidworks, create innovative designs and prototypes. Generate design documentation such as requirements specification, schematics, DFMEA, verification test procedures and test reports under FDA/TUV and QSR design control practices.

  • Lead technical design reviews as required for new technologies or products. Participate in requirements, peer and design reviews as they pertain to new technologies or products.

  • Produce regular progress reports on assigned projects. Conduct measurements and analysis, design of experiments, create engineering designs, develop plans and keep laboratory notebooks on all projects.

  • Ensure all products are developed in a controlled manner and adhere to global regulatory requirements and plant procedures.

  • Ensure activities on assigned projects are within budget and schedule.

  • Assist in product/process introduction, production troubleshooting, complaint investigation or individual measurement and analysis projects.

  • Collect and analyze pertinent information and make recommendations with respect to project patent opportunities.

  • Monitoring of competitor product releases and evaluation of competitor products when applicable.

  • Keep up to date with current changes in technology and regulatory affairs.

  • Perform operations in accordance with established safe working procedures and general safety rules ensuring that attention is always given to special hazards associated in your area of work.

  • Ensure compliance with relevant company and corporate requirements and legislation governing health and safety as principally contained in Safety, Health and Welfare at Work Act 2005 and the Safety, Health and Welfare at Work (General application) regulations 1993.


Skills/Experience



  • Engineering degree or equivalent with a thorough working knowledge of engineering principles essential.

  • Designer of Medical device technologies or products for 7 or more years in the medical device industry is required.

  • The successful candidate has demonstrated design and implementation of technologies into qualified medical devices.

  • Experience in plastics fabrication processes, mintab and SolidWorks required.

  • Demonstrated utilization of Design for Six Sigma design for manufacture/assembly and design for test methodologies highly desirable.

  • Effective communicator, well organized self starter, willing to work in a cross functional environment. Ability to travel internationally when required.


If you would like further Information you can contact the recruiter directly:

James Cassidy | Tel: +353 (0) 1 5079250


PLEASE APPLY DIRECTLY BY CLICKING HERE


Under the Data Protection Acts 1988 and 2003, your details will be kept confidential and will not be passed to a third party without your express prior consent.


Science Recruitment | Science Jobs | Engineering Jobs | Scientific Jobs
Pharmaceutical Jobs | Medical Device Jobs | Clinical Research Jobs | Biotechnology Jobs
Regulatory Affairs Jobs | Quality Assurance Jobs | Pharma Sales Jobs | Supply Chain Jobs