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Waterford Medical Jobs

Medical Jobs in waterford

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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.

REGULATORY AFFAIRS SPECIALIST

Lake Region Integer Corporations Holdings

9 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 - We are one of the world’s largest medical device outsource manufacturers.

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.

Medical device and/or pharmaceutical industry experience preferred - The Senior Manufacturing Engineer role is a role within the plant's Engineering group. It is a highly technical role required to support, debug and improve highly automated manufacturing systems.

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Excellent opportunity for a Facilities Engineer in a fast growing medical devices company based in Waterford city. Excellent role in a fast growing medical devices company based in Waterford city. Experience of working in a medical device/pharmaceutical environment advantageous

Highly respected and established medical devices company in South East. 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

Recognized as a technology leader, Sanmina provides end-to-end design, manufacturing and logistics solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, computing and storage, medical, defense and aerospace, industrial and semiconductor, multimedia, ...

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 - Regulatory Compliance Manager. Waterford - Quality oversight of Change Management - Regulatory support for regional RA to support the business

Lead, develop and enrich a large manufacturing operations team at our world-class Medical Device facility - Drive performance through setting example, motivating others and showing expertise - Oversee all production activities including, KPIs, Yields, Downtime, Quality Metrics and the utilization of machinery & human resources

3-6 years’ experience in a manufacturing environment (high volume automated assembly experience would be an advantage as would medical device manufacturing experience). For more information on our Recruitment and HR Services and to see a full list of our available jobs across Ireland, please visit our website

QA/RA SUPERVISOR

Lake Region Integer Corporations Holdings

9 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 .

Develop and implement new technologies, controls and vision systems to improve cost and quality of existing strategic medical device products - Experience with medical device or clean room environment a plus - Desirable: Experience with equipment build, process automation, machine vision systems development and medical products a plus.

Shift Lead Engineer

Bausch & Lomb Ireland

5 company reviews

Knowledge of medical device and/or pharmaceutical production preferred (cGMP / FDA regulated environment). The engineering/ maintenance roles are concerned with getting high output from our automation- intensive production lines. Engineers working on four-cycle shift will lead teams of technicians to this objective in our new state-of the-art factory.

Projects Automation Engineer

Bausch & Lomb Ireland

5 company reviews

Develop and implement new technologies, controls and vision systems to improve cost and quality of existing strategic medical device products. Desirable: Experience with equipment build, process automation, machine vision systems development and medical products a plus.

QUALITY SENIOR SUPERVISOR

Lake Region Integer Corporations Holdings

9 company reviews

5 years medical device experience essential - The Quality Senior Supervisor will primarily be responsible for maintaining and improving where necessary all quality systems and monitoring production process for compliance to implemented process controls.

3-6 years' experience in a manufacturing environment (high volume automated assembly experience would be an advantage as would medical device manufacturing experience). Job; Automation; Engineer; Medical; Waterford; Mechanical]]> My client is currently recruiting for an Automation Engineer to join their busy manufacturing company based in the south east.

  • See description
  • Updated 19/01/2018
  • Waterford

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 - You will receive competitive salary plus bonus, very generous holiday allowance, pension and VHI healthcare

Medical device and/or pharmaceutical industry experience preferred - Develop \ design and implement cost justified process and equipment improvements. Provide consultative support to the Manufacturing and Maintenance groups. Utilise Lean Six Sigma tools and data to drive continuous improvement. Develop and Implement Safety and Quality improvements.

Senior Manufacturing Engineer

Bausch & Lomb Ireland

5 company reviews

Experience Perferred in: High volume manufacturing, automation, injection moulding/tooling, medical device manufacturing. Medical device, pharmaceutical or High Volume industry experience preferred - The Senior Manufacturing Engineer role is a role within the B&L Ireland Plant Engineering group.

Experience working in a Medical device or Pharmaceutical production environment. This is a permanent position. Safety compliance. GMP Compliance. Develop, Design and Implement Automated Manufacturing systems and Control software applications. Lead cross functional team to deliver project milestones on time and within budget.

The role of General Nurse makes you part of a collaborative, fast-moving nursing team in the Medical/Surgical Ward. This opportunity is for a Registered General Nurse with experience in Hospitals.

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

3 plus years experience in a manufacturing environment (high volume automated assembly experience would be an advantage as would medical device - Process Engineer / Automation Engineer to support design, buy-off, installation and validation of automated production lines.

Develop and implement new technologies, controls and vision systems to improve cost and quality of existing strategic medical device products. Experience with medical device or clean room environment a plus. Desirable: Experience with equipment build, process automation, machine vision systems development and medical products a plus.

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