Director - Talent Services at Drew Consulting
Our client is a leading supplier of bathroom accessories for people with reduced mobility. With over 20 years’ experience in the industry and a global footprint, they take pride in comfort, safety and innovative product design. The Company's ongoing research and development means that they remain an industry leader in a number of sectors, including healthcare. They continually strive for excellence and are proud of the fact that they operate in line with a number of ISO’s and EU Directives.
This position is based in Dublin City Centre and offers the right candidate the opportunity to develop skills and grow within a dynamic international company.
This position is ideal for:
* Someone looking to start or grow their career in a regulated industry, especially medical devices.
* Has genuine interest in quality systems (ISO 13485), regulatory frameworks (MDR), and environmental standards (ISO 14001).
* Wants to gain experience in compliance, audits, and continuous improvement.
Full training will be provided, and you will work closely with various team members across departments.
Key Responsibilities:
Quality Management (Medical Devices):
* Assist in maintaining and improving the Quality Management System (QMS) in accordance with ISO 13485 and EU Medical Device Regulation (MDR 2017/745) requirements.
* Support document control, internal audits, CAPAs, and quality-related investigations.
* Participate in supplier qualification and monitoring processes.
* Contribute to product and process risk assessments.
* Assist in preparing technical documentation and supporting regulatory submissions.
Environmental & Sustainability:
* Support the implementation and maintenance of the ISO 14001 Environmental Management System.
* Participate in environmental compliance activities, including data collection and reporting.
* Assist in sustainability initiatives, including resource efficiency, waste reduction, and circular economy efforts.
* Help monitor and communicate environmental performance indicators.
Cross-functional Support:
* Work collaboratively with production, regulatory, and R&D teams.
* Assist with training and awareness activities related to quality and sustainability.
Key Requirements:
* Third level qualification in a relevant field (an advantage)
* Highly organised and capable of managing multiple projects simultaneously
* Conscientious, highly focused and detail orientated
* Excellent organizational and time-management skills
* Willingness to learn and support different teams with a positive and proactive attitude
* Strong verbal and written communication skills
* Ability to work independently and collaboratively as part of a team
* English required; Italian is an advantage
* Knowledge of or internship experience with ISO 13485, MDR, and/or ISO 14001 is a strong plus.
Seniority level
* Entry level
Employment type
* Full-time
Job function
* Administrative, Quality Assurance, and Management
Industries
* Medical Equipment Manufacturing, Manufacturing, and Hospitals and Health Care
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