Quality Engineer in Medical Devices / Pharma
This 3-month contract is an opportunity to support the development of innovative medical technologies that improve health and quality of life. The position involves working with a global leader in providing medical solutions.
As a Quality Engineer, you will play a critical role in ensuring compliance and driving improvements in manufacturing processes. Your responsibilities will include leading the creation and updating of pFMEAs for catheter manufacturing processes, managing change control activities using electronic QMS, and supporting Test Method Validations (TMV) in collaboration with cross-functional teams.
* Lead the creation and updating of pFMEAs for catheter manufacturing processes.
* Manage change control activities using electronic QMS.
* Support Test Method Validations (TMV) in collaboration with cross-functional teams.
* Ensure all documentation complies with regulatory and quality system requirements.
* Work independently and contribute to impactful medical technologies.
Requirements:
* Minimum 5 years' experience in the Medical Devices or Pharmaceutical industry.
* Bachelor's degree in Engineering or related discipline.
* Proven track record with pFMEA development and eQMS platforms.
* Strong understanding of medical device regulatory standards.
* Excellent problem-solving, documentation, and communication skills.
Contract Details:
* Duration: 3 Months
* Start: Immediate
* Location: Annacotty, Limerick (On-site)
Benefits:
* Opportunity to work with a collaborative and supportive team.
* Chance to contribute to impactful medical technologies.
* Competitive hourly/daily rate.