Senior Quality Systems Engineer
Full time- Fixed Term (5 month Contract)
Galway- Hybrid
As a Senior Quality Systems Engineer at Veryan you will have the opportunity to work alongside experienced professionals in a dynamic collaborative environment where you will play a key role in supporting meaningful and high-impact projects.
What You Will Do:
To ensure Veryans Quality Management Systems (QMS) are compliant with the relevant directives and regulations you will be responsible for the following activities:
- To maintain the CAPA and Complaint Systems.
- To manage Quality Systems data collection and analysis.
- Prepare and present Monthly Quality Reports.
- Complete GAP assessments on Quality Management System regulations
- Support Software Validation activities
- Support the Management Review Process.
- Support the maintenance and continuous improvement of the QMS processes.
- Support other Quality system activities e.g. Audit Management SOP Updates Document System Management.
What Do You Require:
- Educated at minimum to a Diploma Level in Engineering Science or Quality Assurance discipline.
- A minimum of five years relevant experience in the medical device or pharmaceutical industry.
- Familiarity of ISO13485 ISO14971 Medical Device Regulation 2017/745 and FDA QMSRs.
- Good communication and organisational skills and the ability to present reports neatly and accurately.
- Training/Qualification in Quality Systems Risk Management Complaint CAPA management Auditing and Medical Device regulations is highly desirable.
Benefits of Working with Veryan:
- Competitive salary and bonus.
- Pension scheme with generous employer contributions.
- Private medical insurance for you spouse / partner and dependents.
- Paid sick leave & Group life cover.
- Hybrid working and flexible start and finish times.
- Active Sports and Social Committee with a schedule of events taking place during the year.
- Opportunities for further education training and development.
Our Company Values:
- Collaborative- We respect one another and work as a team toward a common goal.
- Innovative- We are passionate and think big with our innovations.
- Empowering- We support and recognise the achievements of one another.
- Patient-Centric- We are committed to excellence.
- Acting with Integrity- We are transparent and do what is right.
Please find information on the processing of your personal data in theApplicant Privacy Notice
Required Experience:
Senior IC
Senior Quality Systems EngineerFull time- Fixed Term (5 month Contract)Galway- HybridAs a Senior Quality Systems Engineer at Veryan you will have the opportunity to work alongside experienced professionals in a dynamic collaborative environment where you will play a key role in supporting meaningful...
Senior Quality Systems Engineer
Full time- Fixed Term (5 month Contract)
Galway- Hybrid
As a Senior Quality Systems Engineer at Veryan you will have the opportunity to work alongside experienced professionals in a dynamic collaborative environment where you will play a key role in supporting meaningful and high-impact projects.
What You Will Do:
To ensure Veryans Quality Management Systems (QMS) are compliant with the relevant directives and regulations you will be responsible for the following activities:
- To maintain the CAPA and Complaint Systems.
- To manage Quality Systems data collection and analysis.
- Prepare and present Monthly Quality Reports.
- Complete GAP assessments on Quality Management System regulations
- Support Software Validation activities
- Support the Management Review Process.
- Support the maintenance and continuous improvement of the QMS processes.
- Support other Quality system activities e.g. Audit Management SOP Updates Document System Management.
What Do You Require:
- Educated at minimum to a Diploma Level in Engineering Science or Quality Assurance discipline.
- A minimum of five years relevant experience in the medical device or pharmaceutical industry.
- Familiarity of ISO13485 ISO14971 Medical Device Regulation 2017/745 and FDA QMSRs.
- Good communication and organisational skills and the ability to present reports neatly and accurately.
- Training/Qualification in Quality Systems Risk Management Complaint CAPA management Auditing and Medical Device regulations is highly desirable.
Benefits of Working with Veryan:
- Competitive salary and bonus.
- Pension scheme with generous employer contributions.
- Private medical insurance for you spouse / partner and dependents.
- Paid sick leave & Group life cover.
- Hybrid working and flexible start and finish times.
- Active Sports and Social Committee with a schedule of events taking place during the year.
- Opportunities for further education training and development.
Our Company Values:
- Collaborative- We respect one another and work as a team toward a common goal.
- Innovative- We are passionate and think big with our innovations.
- Empowering- We support and recognise the achievements of one another.
- Patient-Centric- We are committed to excellence.
- Acting with Integrity- We are transparent and do what is right.
Please find information on the processing of your personal data in theApplicant Privacy Notice
Required Experience:
Senior IC
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