What you need to know

A leading Irish-owned medical devices company that offers innovative manufacturing solutions to their clients is currently seeking an experienced and committed Senior Quality Engineer to join their team.

As a Senior Quality Engineer, you will report directly to the Quality Manager on-site and ensure quality systems are maintained to the highest of standards and that product quality and documentation processes are adhered to.

The company prides itself on its customer-focused approach, outstanding manufacturing processes, and high-quality standards. The company’s cutting-edge facility has grown rapidly in recent years to meet the ever-evolving needs of its growing customer base and is looking for a Quality professional who wants to be part of a dynamic and progressive organisation.
This is a permanent role with an excellent salary and package.

Your new job

Key duties & responsibilities include:

• Select appropriate techniques for problem-solving and make consistent Engineering and Quality Assurance recommendations.

• Make decisions related to product quality including the disposition of non-conforming products.

• Participate in Customer Complaints investigation for your designated area.

• Review and approve operational, test, and validation data to establish technical specifications and performance standards for newly designed or modified products and processes.

• Oversee audits of all quality system categories to assess compliance to process excellence standards.

• Champion continuous improvement and innovation from a quality perspective.

• Work with EHS to identify significant environmental impacts and help to establish goals and targets around significant environmental impacts.

• Liaise with suppliers, and other engineering disciplines internally and externally.

• Provide technical guidance to Quality Engineers, Associate Quality Engineers, Technicians, and other junior members of staff.

• Leads and performs upgrades to Quality System

What are we looking for?

• Bachelor (Level 8) in Engineering, Sciences, or another relevant discipline.

• At least 5 years of experience in the Medical Device industry or a similar highly regulated manufacturing environment.

• Team player with a strong work ethic who enjoys working with others.

• Strong written and verbal communication skills.

• Experience in managing and motivating personnel is an advantage but not essential.

• Experience or ability to manage cross-functional team meetings.

• The ability to establish rapport with internal and external customers, peers, and employees in all departments.

• Significant knowledge of validation engineering and strong familiarity with all regulatory requirements.

• Excellent organizational skills with the ability to effectively

Apply for this job now by sending a Word version of your CV or get in touch with Oliver at oliver@matrixrecruitment.ie

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