Cache of job #14014714

Job Title

Supplier Quality Engineer -

Employer

Sanderson Recruitment Ireland

Location

Offaly

Description

Supplier Quality Engineer. This key role is to support quality engineering activities with regards to supplier quality management & compliance related projects, ensuring technical correctness, & compliance with requirements of global regulations. It is an essential function in the overall strategy for improved assurance of continuity & improvement of established QMS & to support the company growth. RESPONSIBILITIES. Maintain oversight of current suppliers & assess potential new suppliers & service providers for technical, quality, & quality system capabilities. Implement continuous & innovative improvements with demonstrated & measurable results. Drive supplier audit program through managing & conducting supplier audits per schedule. Ensure proper root cause is determined & implemented by supplier for findings. Evaluate nonconforming supplied material & prepared Supplier Correction Action Requests (SCAR) to effective resolution of root cause problems contributing to unsatisfactory supplier quality performance. Ensure supplier files are compliant with regulations & internal procedures. Partner with Site purchasing & integrate Division Supplier Quality team to leverage cross site competencies & drive improvements. Liaise with Operations, Supply Chain Management, Warehouse, Engineering & NPD to ensure uninterrupted supply of materials. Support NPIs by providing guidance on compliant adherence to company requirements as defined in material specifications, CTQ's, process control plans, quality agreements. Ensure that requirements laid down in quality manual & std operating procedures are adhered too, & provide advice & guidance to other depts. for quality related impacts. QUALIFICATIONS/EXPERIENCE. Degree in Quality, Engineering or a Science discipline. 3-5 years' experience at quality engineering level within a regulated industry, preferably Medical Device Industry. Demonstrable knowledge of FDA 21CFR820 &/or ISO 13485 regulations. Audit experience in conduction supplier & or internal audits. Certified Lead auditor qualification for ISO 13485 is an advantage. Knowledge in statistical methods & use of ISO 14971:2007. Good project planning & organizational abilities. Strong interpersonal & communications skills, including oral & written reports. Pro-active with proven ability to work under own initiative, & strong team player. Solid technical ability. Willingness to travel as part of duties. This job originally appeared on RecruitIreland.com.

Date Added

13 days ago

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