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

Validation Engineer


Reference:TG - Validation Engineer Location: Athlone
Cavan
Connaught
Donegal
Leitrim
Longford
Midlands
Offaly
Roscommon
Sligo
Qualification:DegreeExperience:1-2 Years
Job Type:PermanentSalary: Not Disclosed

Role: Validation Engineer
Location: Carrick on Shannon, Leitrim
Benefits: Competitive salary, Bonus, pension, healthcare and hybrid working


Company:
Work with theLargest employer in Leitrim show specialise in making Catheters all inhouse. Work in a company have cleanrooms dedicated to customers, very specialised. Generally have about 100 promotions per year – Projects involved, individual plans, goal setting, leadership training.




Responsibilities

  • Ensuring that product introductions & change controls are effectively managed in accordance with the requirements of ISO 13485.
  • Participation in the new product introductions programmes to ensure that they are effectively introduced in accordance with the requirements of ISO 13845. Generation of Product Technical Files & associated studies
  • Completion of Validation Programme – Risk Analysis, VMP,IQ’s, OQ’s, PQ’s as required according to procedure QAP 030 and other related procedures
  • Adhere to Plant Safety requirements and Health & Safety requirements relating to your work, assuming responsibility for those aspects of the OH&S System over which you have control to ensure the health and safety of yourself and others.
  • Be aware of the potential environmental impacts associated with your work and the implications of non-conformance.
  • Contribute to enhanced energy performance by conservation of energy where possible (Lighting, Equipment, Air Conditioning etc).
  • Contribute to the continual improvement activities of the OH&S, Environmental and Energy Management systems through participation, providing feedback/ suggestions for improvement and by reporting accidents, dangerous occurrence, near miss/ illness, good catch and environmental incidents in a timely manner.



Qualifications
  • Required: Third level qualification in Engineering / Manufacturing / Quality with emphasis on Medical Device / Biomedical. Minimum Bachelor’s degree in a Science / Engineering / Quality related discipline.
  • 1+ years’ experience in a Quality role in Medical Device/Pharmaceutical Environment
  • An Associate position may exist where there is limited experience and will be assigned to an experienced Engineer.



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



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