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Product Development Verification and Validation Engineer, Roscommon
Client:
Cpl
Location:
Roscommon, Ireland
Job Category:
Other
EU work permit required:
Yes
Job Reference:
b5cc69fe32a6
Job Views:
77
Posted:
21.01.2025
Expiry Date:
07.03.2025
Job Description:
On behalf of our client, we are currently recruiting for a Product Development Verification and Validation Engineer for a global medical technology company based in Dublin. There is some hybrid work, approx 1 day a week from home, but this will depend on projects. Therefore, the person must be commutable to Dublin. This role reports to the Technical Director.
Role Overview
This global medical technology company is looking to expand its engineering department to support the development of flagship and next-generation medical device products that combine auditory stimulation, nerve stimulation, wireless communications, and physiological sensing technologies.
The successful candidate will gain exposure to a range of technologies at the forefront of biomedical research and every phase of the product development lifecycle from initial concept development through to commercialization.
The company provides its engineers with a stimulating working environment and opportunities to work on a variety of commercial and research projects as part of a small, motivated, cross-functional team.
Key Responsibilities
1. Test Protocol Development:
o Develop comprehensive test protocols for various testing domains including electronic circuit design verification (DVT), mechanical design verification testing, sound stimulation functional testing, electrical stimulation functional testing, packaging integrity testing, transport validation, ingress protection testing, electromagnetic compatibility testing, and wireless coexistence testing.
o Collaborate with design and development teams to ensure test protocols are aligned with design requirements, manufacturing requirements, and applicable regulatory requirements.
2. Test Execution:
o Participate in bench testing of medical device products based on the developed protocols, ensuring rigorous and thorough execution.
o Oversee third-party or internal team testing activities, ensuring adherence to protocols and the integrity of the test results.
o Analysis of test results, including the application of statistical methods where appropriate.
o Documentation of the test results, ensuring accurate record-keeping and comprehensive traceability.
3. Design & Development Support:
o Participate in the design change control process, ensuring that any changes made to the product design are verified, validated, and meet the requirements of applicable procedures and regulations.
o Collaborate with design and development teams, offering feedback and guidance based on testing outcomes to refine the design.
o Engage in risk analysis activities, identifying potential design and usage risks, and ensuring they are adequately assessed, controlled, and reported.
o Assist with document control, ensuring that all design, test, and validation documentation is properly maintained, updated, and compliant with applicable QMS procedures.
4. Manufacturing Equipment Development & Validation:
o Participate in the design, development, and validation of manufacturing equipment, particularly focusing on printed-circuit board test fixtures.
o Collaborate with manufacturing and quality assurance teams to ensure equipment meets both production and regulatory requirements.
o Validate manufacturing equipment and tools, ensuring they are fit for purpose and meet the defined specifications.
5. Continuous Improvement, Training and Collaboration:
o Stay updated with the latest industry standards, regulations, and best practices related to verification and validation.
o Provide training to junior team members or cross-functional teams on best practices in design validation and verification.
o Continuously seek opportunities to improve testing methodologies, tools, and processes.
o Work closely with other departments, including design, manufacturing, regulatory affairs, and quality assurance, ensuring alignment of goals and seamless communication.
o Present test findings to relevant stakeholders, ensuring clarity of results, inferences, and conclusions of the results and their associated implications for the product development process.
Qualifications / Skills / Attributes
* Degree in Engineering or related fields (Electrical, Electronic, or Mechanical Engineering preferred) with 5+ years' industry experience in an engineering role.
* An understanding of quality management system principles (e.g., ISO) and/or FDA design and development processes.
* At least one year of experience in electrical and/or mechanical verification (Design Verification Testing/DVT), including drafting test protocols, executing or overseeing testing, and authoring test reports.
* Experience and/or knowledge of risk management techniques, e.g., FMEA.
* Experience in Design for Test (DFT) and Design for Manufacture (DFM).
* PC literacy (MS Word, Excel, PowerPoint) and familiarity with project management tools such as MS Project or SmartSheet.
* A team player with excellent interpersonal, communication, and problem-solving skills.
* Ability to present ideas and concepts clearly and effectively to all levels of the company.
* Experience in design and testing for electromagnetic compatibility (EMC).
* Knowledge of international safety standards such as IEC.
* Experience in the application of statistical principles within an engineering discipline, including sample size calculations and statistical analyses, with experience in the use of statistical software such as R, STATA, or Matlab.
For full details contact Linda at 1 or email your CV to. Thornshaw Scientific is a division of the CPL Group
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