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Westmeath
Wexford
Republic of Ireland
Outside EU
Westmeath
Dublin City Centre
Galway
Dublin
Dublin
Galway
Dublin
Galway
Dublin South
Cork
Westmeath
Dublin West
Dublin
Limerick
Galway
Dublin
Waterford
Galway
Dublin South
Limerick
Westmeath
Cork
Dublin
Galway
Dublin South
Republic of Ireland
Waterford
Limerick
Dublin
Westmeath
Dublin
Cork
Dublin North
Dublin
Dublin
Dublin
Kildare
Dublin
Dublin West
Dublin
Waterford
Dublin
Dublin
Dublin
Dublin
Dublin
Dublin North
Dublin
Limerick
Westmeath
Dublin
Dublin
Dublin North
Meath
Dublin
Dublin
Cork
Dublin
Cork
Tipperary
Dublin West
Galway
Kildare
Dublin West
Dublin
Cork
Sligo
Dublin
Offaly
Westmeath
Dublin North
Australia
Galway
Galway
Cork
Republic of Ireland
Sligo
Dublin West
Dublin
Dublin
Dublin
Dublin North
Munster
Galway
Dublin
Republic of Ireland
Dublin
Galway
Dublin
Limerick
Dublin
Dublin
Design Assurance Engineer - CN003
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| Reference: | ACKW-756140 | Location: |
Galway |
| Qualification: | Certificate | Experience: | 3-4 Years |
| Job Type: | Permanent | Salary: | Not Disclosed |
Our Client is a Medical Device company based in Galway. They are currently looking for a Design Assurance Engineer to join their team. This position provides QA Technical and compliance expertise as part of teams tasked with establishing customer needs, developing new products and/or modifying existing designs.
KEY RESPONSIBILITES
• Responsible for compliance of product development, risk management and post market activities with company Policies and Procedures and applicable International Regulations.
• Work as part of product development team in identifying and translating user requirements into design requirements, identifying critical design features and components.
• Complete verification, design validation and test method validation activities associated with product development ang implementing design/process changes.
• Work with R&D and manufacturing engineering in translating design requirements into manufacturing requirements, including the development of manufacturing test methods and implementing production monitoring and controls.
• Resolve project issues by working with team members, suppliers, and others as appropriate. Apply thorough, systematic problem -solving methodologies in identifying, prioritising, communicating, and resolving quality issues.
• Monitor compliance with company policies, procedures and applicable regulatory requirements, identifying and implementing process and system improvements.
• Leads and/or facilitates compliance and improvement activities associated with the company quality system (e.g. CAPA).
• Demonstrate an ability to apply, recommend and/or create quality tools and apply them effectively to a variety of business situations related to product development, and post market activities.
ESSENTIAL SKILLS/ EXPERIENCE:
Minimum Bachelor's Degree in Engineering, Science or related technical field, and a 3 years minimum QA, Quality System or regulatory experience in the medical industry a prerequisite. The successful candidate will need a strong technical aptitude with an excellent understanding of their subject matter. Be highly motivated and an enthusiastic self-starter with the ability to work under own initiative and as a team player.
KEY RELATIONSHIPS/ INTERFACES: Regulatory, R&D, Clinical, Marketing, Operations, Distribution, External Services Suppliers
BEHAVIOURS VALUES
Strong work ethic, combined with creativity, initiative and great technical capability. Excellent presentation and verbal communication skills are essential.
Clodagh Nerney | Tel: +353 (0) 1 507 9254
Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: info@lifescience.ie | Copyright © 2012 Life Science Recruitment Ltd
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