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Thomas Gallagher
Life Science

+353870612325
[email protected]
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Details

Quality Engineer


Reference:TG - QE - Oranmore Location: Galway
Galway City
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: QE Manufacturing Engineer, Quality Assurance Technologist, Quality Engineer, Quality Specialist, Quality Systems Engineer, Quality Systems Lead, Quality Systems Specialist, Senior Quality Engineer

Job title: Quality Engineer
Location: Oranmore, Galway
Benefits: Excellent salary, Income Protection, Life Assurance, Contribution of €2,000 per annum in lieu of health insurance, Pension Scheme, Annual discretionary bonus up to 10%, Educational Assistance, Employee Referral Programme, Cycle to Work Scheme, Sports & Social Activities



Role:
As a Quality Engineer you will join the Operations team. And play a pivotal role in ensuring the quality and compliance of our manufacturing processes, contributing to the delivery of medical devices that change lives.



Company:
My client have developed a product on the market which is an effective option for both long-term and newly diagnosed chronic rhinitis patients.


Responsibilities:
- Develop, implement, and maintain quality assurance procedures and methods for control of materials and finished goods
- Work as a key member of the operations team and with suppliers to ensure quality standards are met and maintained.
- Develop and execute product quality control plans, documents and procedures.
- Provides input to risk analyses and Process Failure Mode Effect Analysis’ (pFMEAs) including with suppliers.
- Implement and enhance quality principles, gather and analyse quality data to support product/process improvement activities. .
- Oversee manufacturing related quality events in line with GMP and internal procedures, including process defects, CAPA, and complaint investigations. Disposition non-conforming material and work with manufacturer and suppliers to implement corrective and preventive actions.
- Provide quality guidance as an integral member of the operations team, influencing manufacturing activities.
- Provide quality input into process validation activities.



Requirements:
- BE/BS Degree. A Post-graduate qualification in Quality Assurance is preferable although not mandatory.
- At least three years Quality Engineering experience or related role within the medical device industry.
- Experienced working in a medical device manufacturing environment complying with Good Manufacturing Practices.


Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on 087 0612325 OR [email protected]