- Posted 23 January 2023
- Job type Permanent
- Contact NameDavid Rooney
What you need to know
Matrix Recruitment is working with our client who are an innovative and growing medical devices company in Co. Roscommon to hire a Quality Assurance Engineer.
The company provide tailored technical solutions and manufacturing services to an array of leading med-tech companies.
As a Quality Assurance Engineer will provide ongoing Quality support to maximise production quality performance and implement corrective/preventative action on all quality issues in production. You will address any issues identified in the manufacturing process and validation of new processes/products ensuring effective implementation of required QMS documentation. You will report to the Quality Engineering Manager.
This is a Permanent role with an excellent salary and benefits and an exciting opportunity for a Quality Assurance Engineer to join an excellent team in a fast-paced environment.
Your new job
Key duties & responsibilities:
Implement and adhere to the companies Quality Management systems.
Review, update and maintain existing quality management processes and procedures.
Maintain detailed and accurate quality records, data analysis and documentation.
Initiate and drive continuous improvement programs.
Lead Quality Engineering activities for the introduction of new production lines and existing product lines.
Coordinate process and product validations.
Provide quality input to cross functional teams to support existing product lines.
Investigate root cause of quality issues and following through with timely and effective corrective actions.
Oversee non-conforming material, customer complaints, CAPA investigations, analysis, and improvement.
Conduct internal audits and external audits as required.
Mentor and offer support to Junior members of staff on policies and procedures.
What are we looking for?
Level 8 or equivalent Degree in Quality Assurance or a relevant discipline.
3 + years’ experience in a Quality Engineering role, preferable in the medical device sector.
Strong team player who can work well in multifunctional teams and manage internal and external customers’ requirements.
Effective communicator and influencer across multi-functional teams
Proficient with Syspro, Minitab & Lotus Notes, is desirable.
Knowledge of ISO 13485, ISO 14971 and QSR 21 CFR Part 820 standards.
Strong proficiency in statistical analysis techniques to investigate and solve problems and improve quality.
Ability to plan, organise, and prioritise own daily work routine to meet established schedule.
Ability to drive projects to completion.
Please send cv in word format.
Call David for more information on this job on 087 4054758 / email@example.com
Please note that due to the expected high volume of applications we can only reply to applicants suitable for the position. In the interest of protecting your data and informing you of your rights we will notify you should we retain your information by issuing an acknowledgement email and a request for consent where not already expressly given.
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