I'm currently hiring for a Quality Engineer role with a Medical Device company in Sligo. This is a perm role with strong salary and benefits. Full time on site. If you are interested, please apply below and I'll be in touch if your CV is a fit.
Responsibilities:
* Provide technical quality support to Project Manager, Design Engineers, Production manager and clients.
* 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 sterilised product.
* Quality review of SOPs, Work instructions, templates, 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.
* Updates job knowledge by participating in educational opportunities.
* Other such duties as may be assigned from time to time by their manager.
Qualifications:
* Minimum 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 requirements.
* 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.
* Demonstrate detailed working knowledge of the medical device industry.
* Excellent written and verbal communication skills, with the ability to communicate appropriately with different Engineering teams, Project Management, suppliers and customers.
* Self-motivated, flexible with a desire to learn new tasks.
* Excellent attention to detail with strong numerical and problem-solving ability, while maintaining awareness of longer-term objectives.
* Capacity to maintain the highest level of confidentiality internally and externally.
* High level of teamwork and engagement.
Seniority level
Associate
Employment type
Full-time
Job function
Quality Assurance
Industries
Medical Equipment Manufacturing
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