Quality Systems Engineer
Full time (39 hour)- Temporary maternity cover role – initial 6 month contract with possibility for extension
Galway (Hybrid)
We have an exciting opportunity for a Quality Systems Engineer to join Veryan Medical!
Summary
Veryan Medical is a fast-paced, rapidly growing medical device company offering a highly differentiated solution in SFA interventions. We share a commitment, a passion, and a vision for the contribution Veryan makes to innovation in interventional medicine.
Our team powers Veryan’s business. Whether sales representatives, design engineers, quality engineers, or clinical study managers, our people bring an unmatched expertise in each of their fields that both inspires and challenges.
Veryan’s culture of innovation helps each individual develop both professionally and personally, and our culture of respect means that we all work in a collaborative, empowering, and exciting environment. We are committed to excellence through our patient-centric approach, and we pride ourselves in our integrity of doing what is right and doing what we say.
Reporting to the Quality Systems Manager the role of Quality Systems Engineer is a crucial one in Veryan to ensure that our company systems and procedures are compliant as we scale and grow.
Job Requirements
Principal Responsibilities
- Support maintenance of the Veryan Quality Management System.
- Act as CAPA/Complaint/Temp coordinator as required.
- Participate in/support the following activities as required:
- Complaints
- CAPA
- Internal Audits
- External Audits
- Supplier Management
- Document Control
- Training
- Change Control
- Risk Management
- Regulatory Reporting support
- PMS support
- Review Quality System records for completeness and compliance.
- Support investigations and root cause analysis activities.
- Generate and analyse Quality System metrics.
- Support management review preparation.
- Participate in continuous improvement initiatives.
- Other activities as required.
Education & Training
- Educated at minimum to a Diploma Level in Engineering, Science or Quality Assurance discipline.
Experience
- A minimum of two years’ relevant experience in the medical device or pharmaceutical industry.
- Familiarity of ISO13485, ISO14971, Medical Device Regulation 2017/745 and 21 CFR Part 820 is desirable.
- Good communication and organisational skills, and the ability to present reports neatly and accurately is essential.
- Experience in management of Quality Systems activities, in particular Internal/ External Audit, Software Validation Complaints, Risk Management and CAPA is desirable.
Benefits of Working with Veryan:
- Competitive salary and bonus payable on completion of your contract
- Pension scheme with generous employer contributions up to 8%
- Private medical insurance for you, spouse / partner and dependents
- Paid sick leave
- Long term disability cover
- Group life cover
- Annual leave of 23 days plus bank holidays increasing with service (pro-rata depending on length of contract)
- Active Sports and Social Committee with a schedule of events taking place during the year
- Hybrid working – on average 50% of time or 2/3 days a week on site in our state-of-the-art facility in Parkmore
- Flexible start and finish times
- Opportunities for further education, training and development
Company Values
- Collaborative
- Innovative
- Empowering
- Patient-centric
- Acting with Integrity
