About Your New Employer:
Medical device engineering company offering a range of development and manufacturing services from initial design assessment, through to the provision of sterile finished product for the European and US medical device market. This employer provides dynamic and inclusive environment for Employees.
About Your New Job as a Quality Engineer
- Work closely with Engineering team and the client to establish and maintain compliant product specifications.
- Quality review of process validation plan, protocols, and reports.
- Co-ordinate and contribute to the generation and maintenance of compliant product risk management files.
- Issue, review, and release of lot records to manufacturing.
- Co-ordinate and review of testing and release of sterilise product.
- Quality review of SOP’s, Work instruction’s, template’s, Material specifications etc. to ensure compliance to applicable regulatory standards and cGMP procedures.
- Review and approve product change controls.
- Liaise with suppliers and clients on quality related issues.
- Perform an active role in the maintenance, further development and continuous improvement of the QMS.
- Support QMS as quality coordinator in investigation, root cause analysis, disposition, and corrective action of non-conformances & customer complaints.
- Perform CAPA reports.
- Support clients in product submission to applicable regulatory authorities.
- Conduct internal audits and compilation of associated documentation.
- Support and assist in the preparation for customer and surveillance audits.
- Other such duties as may be assigned from time to time by their manager.
What Skills You Need to succeed as a Quality Engineer:
- Degree in a Science or Engineering discipline.
- 3-5 Years’ experience working in a medical device environment.
- Strong knowledge of ISO 13485, FDA regulations 21CFR 820.
- Strong knowledge of MDR & FDA product submission requirement.
- Internal/external auditing experience would be an advantage.
- Validation experience including Sterilization, process and packaging validations would be beneficial.
- Knowledge of Medical Device manufacturing environment including cGMP would be an advantage.
- Strong understanding of the general principles of ISO 14971.
- Strong decision-making ability, coupled with the ability to work on own initiative with minimum supervision and ability to multitask and prioritise is required.
- Excellent written and verbal communication skills, with the ability to communicate appropriately with different Engineering teams, Project Management, suppliers and customers.
- Excellent attention to detail with strong numerical and problem-solving ability, while maintaining awareness of longer-term objectives.
What’s on Offer for Candidates for a Quality Engineer:
- Salary of 40k – 52,5k DOE
- Benefits package: health insurance, pension, educational assistance, flexible working policy
- Fantastic career development opportunities
What’s Next
- Apply now by clicking the “Apply Now" button or call me, Karolina on +353 091749267.
- Or if the job isn’t quite right but you are looking for something similar, please get in touch. We also have multiple Temp, FTC and Contract jobs available.
