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Quality Systems Enginer
Dublin
Dublin
R&D Senior Program Manager
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Manufacturing Engineer
Wexford
Wexford
Process Engineer
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Cork
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Dublin
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Tipperary
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Westmeath
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Republic of Ireland
Republic of Ireland
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Galway
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Dublin
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Carlow
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Carlow
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Carlow
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Dublin
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Associate Global Trade Ops
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Clare
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Republic of Ireland
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Dublin
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Clare
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Senior Validation Engineer
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Limerick
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Westmeath
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Dublin
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Tipperary
Senior Technical Writer
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Head of R&D
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Lead Maintenance Reliability Engineer
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Westmeath
Senior R&D Engineer
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Quality Manager - NPI
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Dublin
Senior Operations Engineer
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Senior Quality Engineer
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Carlow
Senior R&D Engineer
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Dublin
Senior Regulatory Affairs Specialist
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Senior Recruitment Consultant
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Republic of Ireland
Senior Engineering Manager
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R&D Program Manager
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Senior R&D Engineer
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Senior Quality Engineer
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Clinical Affairs Manager
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Carlow
Senior QC Associate
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Dublin
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Carlow
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Project Manager
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Clare
Apply for this job
Details
Quality Engineer
Reference: | CCL (AHPD-441806) | Location: |
Wexford |
Qualification: | Degree | Experience: | 1-2 Years |
Job Type: | Permanent | Salary: | Not Disclosed |
May be suitable for:
EHS Engineer, Quality Engineer
Role:Quality Engineer – Hybrid Role
Location:Enniscorthy, Wexford
Company:
My client are one of the largest global medical technology companies in the world and are advancing the world of health by improving medical discovery, diagnostics and the delivery of care. They have over 75,000 employees and a presence in virtually every country around the world!
Role:
This role is a 18 month fixed term position. It offers hybrid working (3 days in the office and 2 from home) with a competitive salary and package. Reporting to the Senior Quality Engineer, this individual will be a key member of the Supplier Quality team.
Ability to work with the following is an advantage:
- Lead/participate in continuous improvement/CAPA team activities
- Perform risk management activities in a cross-functional environment
- Ensure regulatory compliance in area of responsibility to cGMP’s, with the ability to train others
- Ensure that documentation and work practices comply with ISO and regulatory requirements
- Develop, maintain, and improve the quality management system
- Assess quality management system effectiveness through internal audit and performance review
- Excellent interpersonal skills with the ability to work in a team environment and work under own initiative to targets and deadlines
- Third level technical / Science qualification plus Min 2 years in the medical device or pharmaceutical industry, preferably within supplier management
- Knowledge of quality management systems ISO 13485, GMP
To apply or and for more info call me on 0870608656 or email[email protected]
Project Manager Quality Assurance Clinical Research Dublin PhD Supply Chain Sales and Marketing Chemistry Quality Engineering Scientist IT Limerick Connected Health Quality Control Scientific Product Development Engineer Medical Affairs Biopharmaceutical Manufacturing Executive Validation Engineer Pharma Sales Academic Laboratory Scientist Engineering Microbiology Cork City Cork Medical Device Biotechnology Diagnostics Mayo Packaging Engineer Supply Chain Life Science Allied Healthcare Pharmaceutical Academic Sales and Marketing
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
Valid XHTML - CSS