As a MANAGER OF QUALITY & REGULATORY you will provide hands-on
leadership to the Product Design & Development (D&D) team, and will be
the key person in the areas of Quality Engineering. Provide strategic
project direction and ensure that standards / requirements are
up-to-date and identify compliance gaps and take action to address
them. Work closely with the Operations, Engineering & R&D leadership
teams to drive and grow the business to meet the strategic objectives
of the organization. You will mentor engineers, manage teams and
define appropriate goals and giving direction. While being the subject
matter expert you will mentor and support teams during design cycle
activities, work on Manufacturing, R&D and compliance related
activities and will provide solutions which are highly efficient and
Other responsibilities are:
Interacting with customers, understand what customer wants, getting
clear requirements and setting direction while using your broad
Completing the integration of IFS for Nordson Medical Galway site;
Building a QA Team and manage resource requirements;
Engaging with the design site of the business to enhance project
Implementing Continues Improvement.
EDUCATION AND EXPERIENCE REQUIREMENTS
Degree in Engineering.
Experience in medical device is essential, minimum ten (**Apply on the
Minimum 5 years of Quality leadership, with direct reports is
Experience in Design Control and Product Development essential.
SKILLS AND ABILITIES
Excellent communication skills with ability to interface at all
Ability to recruit and retain high calibre staff, developer of people
through professional and personal mentoring;
Required proficiency in the management of Quality; team player focus;
Excellent computer skills.
**Apply on the website** – **Apply on the website**%, team meetings,
FOR AGENCIES: ACQUISITION REGARDING THIS OR ANY OTHER VACANCY IS NOT
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