Senior Quality Engineer

Direct message the job poster from PE Global

Senior Recruitment Consultant at PE Global

PE Global is currently recruiting for a Senior Design Assurance Engineer on behalf of a leading medical device company based in Galway. This is an initial 12-month contract role.

Responsibilities:

• Support sustaining commercial projects from a Design Assurance perspective. You will be directly involved in making sure our products are maintained through the full product lifecycle and that these products comply with global standards.
• Support the introduction/implementation of product/process/materials changes to the manufacturing operation. You will assess the patient risk appropriately for these design changes. You will provide QA technical direction/input to qualification and validation activities in conjunction with R&D and Mfg. Engineering.
• Responsible for generation of Design Verification protocols & will participate in the compilation of design verification and shelf-life data for regulatory submissions to support design change approval.
• Interface with Regulatory Affairs to ensure information is clearly presented to minimize Regulatory Agency questions.
• Contribute to establishing strong working cross functional relationships across the organization and with partners within a complex technical environment.
• As part of ongoing professional development, you will maintain expert, up to date knowledge of developments in regulatory compliance requirements for product design, development, and commercialization activities. You will generate and approve change requests. Lead investigation analysis and timely completion of same.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
• May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.

Education & Experience:

• Requires a Bachelor's degree and minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience.
• Strong problem-solving skills with the ability to identify root causes and implement corrective actions.
• Strong technical writing ability.
• Provide input to design and manufacturing deliverables including material specifications, drawings, inspection procedures, and manufacturing procedures
• Understand risk management concepts used throughout the quality system to successfully meet FDA, ANSI/AAMI/ISO 14971:2019, and ANSI/AAMI/ISO 13485:2016 requirements.

Interested candidates should submit an updated CV.

Please click the link below to apply, call Paul Wheatley on 083 094 0199 or alternatively send an up-to-date CV to paul.wheatley@peglobal.net

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

Seniority level

• Seniority levelAssociate

Employment type

• Employment typeContract

Job function

• Job functionScience, Engineering, and Quality Assurance
• IndustriesMedical Equipment Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research

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