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Waterford Medical Jobs

Medical Jobs in waterford

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Assembly Operative Medical Device

Schivo Medical

Assembling medical device parts - Previous medical device assembly or small parts assembly - Performs small part assembly of final products and sub-assemblies of medical device products by following released procedures. Assembly Operative - Full-time - Assembly Supervisor

Responsible for the development of global regulatory strategies based on US FDA regulations, European Medical Device Directive, External Standards, and other international regulations - An exciting opportunity has arisen with our client based in the South East for a Regulatory and Compliance Manager - The Role

Shift Production Manager

Bausch & Lomb Ireland

5 company reviews

At least 5 years manufacturing experience, preferably at production management level, within a team-based manufacturing environment (Medical Device background desirable but not essential) Bausch & Lomb are seeking an experience Production Manager (Manufacturing)

An exciting opportunity has arisen with our client based in Waterford for a Regulatory Affairs Site Officer. This is an excellent opportunity to join a progressive organisation

8+ Years relevant work experience in a regulated medical device or pharmaceutical environment - Knowledge and expertise in the area of technical quality oversight for new product platforms at Sanofi Waterford. The position works closely with the Operations functions to design, install, evaluate and improve new product platforms (e.g. PFS, Auto Injector).

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I am delighted to be assisting my client, a world-renowned medical technology company to recruit a Quality Engineer to join their team in Wexford (location is easily commutable to Waterford, Kilkenny, Carrick-On-Suir) This can be from the medical device, food, pharma or automotive sector.

New role for a Chemical Process Engineer to join a large multi-national healthcare company based in the South East.

Perform Failure analysis on electronic medical devices to get to root cause to component level, using electronic schematics and documentation. Reviews or develops processing and/or manufacturing instructions. Work with cross functional groups to improve lean efficiency’s and test system efficiency’s and reduction in production fallout & equipment uptime.

Pharmaceutical or medical device industry experience preferred. This is a permanent job - This Process & Equipment Engineering role is required to design, develop, implement and support manufacturing systems related to the handling of liquid chemicals. Identify, design, develop and implement process and equipment innovations and improvements.

HS&E Engineer

West Pharmaceutical Products Ireland

14 company reviews

3 – 5 years EHS Experience working in a Manufacturing facility – Medical Device/ Pharma or similar - HS7E Engineer required for green field site. Purpose of Job

Regulatory Compliance Manager

Bausch & Lomb Ireland

5 company reviews

Responsible for the development of global regulatory strategies for contact lenses based on US FDA regulations, European Medical Device Directive, External Standards, and other international regulations - Bausch + Lomb are currently recruiting a Regulatory Compliance Manager.

Qualification in a Science Discipline and work experience in Pharmaceutical/Medical Device with two year’s experience in a QA environment, preferably in a validation role. 12 Month contract for a Quality Officer in a leading pharmaceutical company based in Waterford City.

Minimum of 2-3 years direct experience in a Validation Role in either Medical device or Pharmaceutical Industry. This role is a 10-12-month contract and provides an opportunity to work in one of the leading manufacturing companies in Cork.

Chemical Process Engineer

Bausch & Lomb Ireland

5 company reviews

Pharmaceutical or medical device industry experience preferred - Bausch + Lomb are seeking to recruit a Chemical Process Engineer as part of a Plant Expansion / Re-Engineering project

Our client is a highly respected and established medical devices company in the South East. Ensuring continuous compliance with various regulatory standards and inspections including; FDA, Medical Device Directive and any other applicable market regulation

Process Discipline Manager

DPS

Team management experience within project engineering, pharma / bio life sciences, medical devices, microelectronics or similar industry. Reporting to the Engineering Manager the Process Discipline Manager has technical, quality, managerial and administrative responsibility for the Process department.

New role for an Electronics Test Technician in a world class medical devices manufacturing company based in South Tipperary. Utilises electronic engineering debug techniques to identify root cause on electronic printed circuit boards and test systems, used for manufacture of implantable medical devices.

Regulatory Affairs Specialist

Lake Region Integer Corporations Holdings

8 company reviews

Experience 2-3 years experience in a similar regulatory role, quality assurance role in the pharmaceutical, healthcare or medical device sector essential, preferably in an FDA regulated environment Medical Device Directive - ISO13485 Medical Device Quality Management System

We require Care Assistants to become an integral part of a dynamic and progressive team. The successful candidates will provide support and follow relevant programmes for adults with an intellectual disability.

QA/RA SUPERVISOR

Lake Region Integer Corporations Holdings

8 company reviews

Medical Device Directive - ISO13485 Medical Device Quality Management System - Minimum 3-5 years experience in a Medical device quality systems role in an FDA regulated environment - The QA/RA Supervisor is responsible for the supervision of development, maintenance, and distribution of quality documents within the Quality Management System .

Senior Architectural Technican

DPS

Significant previous experience of working in a high spec environment i.e. pharmaceutical; semiconductor or medical device is a requirement. The successful will have a minimum of 5 years’ experience working in a high spec environment i.e. pharmaceutical; semi-conductor or medical device is a requirement for this job opportunity.

Project Engineer (Building Services/Mechanical)

DPS

Experience of working in a live environment (pharmaceutical/medical device) the successful Mechanical Project Engineer will have a proven understanding of HVAC, BMS, Utilities and facilities with previous experience of HVAC commissioning an advantage.

Qualification in Engineering/Science Discipline and work experience in Pharmaceutical/Medical Device with two years’ experience in a QA environment. Always on the look out for Quality Officers. Have a look at this job spec and if you want to find out more, please give me a buzz.

  • See description
  • Updated 08/11/2017
  • Waterford

The doctor job is based in a healthcare facility in Ireland and offers an top rates of pay along with initial accommodation and transport assistance, and will continue to the following medical rotation.

As the Quality Engineer you will work for our client, a Medical Device company. Minimum of 3 years previous relevant industrial experience of working in an ISO9001, ISO13485, cGMP or other suitable quality position preferably the Medical Device sector. Step Forward.

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