Research & Development Engineer
Limerick | Contract | www.cv-library.ie |
Hybrid (1-3 days on site)
Headcount Solutions is seeking an experienced R&D Engineer for a leading Medical Devices Facility. As part of the R&D Team you will be responsible for:
Biomaterial Development: Research, develop, and test novel biomaterial coatings for cardiovascular implants with a focus on functionality, biocompatibility, and durability.
Laboratory Work: Design experiments, analyse data, and optimize processes to meet performance and regulatory requirements.
Cross-functional Collaboration: Work closely with a diverse team of scientists, engineers, and regulatory experts to ensure project alignment with regulatory and quality standards
Documentation: Maintain comprehensive records, documentation, and reports to ensure regulatory compliance and intellectual property protection.
Project Management: Take ownership of assigned projects, managing timelines, budgets, and resources effectively.
Requirements:
• Bachelor's, Master's, or Ph.D. in Biomedical Engineering, Materials Science, Chemistry, or a related field.
• Min 2-3 years’ experience in the design & development of Class III medical devices, including familiarity with medical device regulations, and relevant standards (e.g., ISO 13485).
• Strong background in eg. Biomedical Engineering (Biosciences), with experience of biological analytical techniques
• Industrial experience in design & development of Class III medical devices.
• Familiarity with functional biomaterial coatings would also be an advantage.
For immediate consideration please forward your CV together with a covering note outlining your relevant experience for the position.
Due to the urgency of the position we are unable to process work visas for non-EU applicant
Headcount Solutions is seeking an experienced R&D Engineer for a leading Medical Devices Facility. As part of the R&D Team you will be responsible for:
Biomaterial Development: Research, develop, and test novel biomaterial coatings for cardiovascular implants with a focus on functionality, biocompatibility, and durability.
Laboratory Work: Design experiments, analyse data, and optimize processes to meet performance and regulatory requirements.
Cross-functional Collaboration: Work closely with a diverse team of scientists, engineers, and regulatory experts to ensure project alignment with regulatory and quality standards
Documentation: Maintain comprehensive records, documentation, and reports to ensure regulatory compliance and intellectual property protection.
Project Management: Take ownership of assigned projects, managing timelines, budgets, and resources effectively.
Requirements:
• Bachelor's, Master's, or Ph.D. in Biomedical Engineering, Materials Science, Chemistry, or a related field.
• Min 2-3 years’ experience in the design & development of Class III medical devices, including familiarity with medical device regulations, and relevant standards (e.g., ISO 13485).
• Strong background in eg. Biomedical Engineering (Biosciences), with experience of biological analytical techniques
• Industrial experience in design & development of Class III medical devices.
• Familiarity with functional biomaterial coatings would also be an advantage.
For immediate consideration please forward your CV together with a covering note outlining your relevant experience for the position.
Due to the urgency of the position we are unable to process work visas for non-EU applicant
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