The Role

• Contribute to the evaluation and selection of global best-in-class suppliers.

• Engage with suppliers to execute process qualification plans and reports to assure components and materials.

• Represent the organization as the primary supplier liaison on component quality issues.

• Lead global supplier quality system audits, ensuring timely and appropriate action are taken.

• Assess supplier processes for optimum output, process stability and controls, identifying and implementing strategies for continual quality improvement and control.

• Develop and certify suppliers to achieve Dock to Stock status for supplied components.

• Review and disposition supplier change requests, coordinate activities with suppliers and with internal cross-functional support teams to develop and implement appropriate strategies to qualify and support the change.

• Third level degree in Engineering or Science isessential for this role

• At least 2 years’ experience working in an engineering function preferably within Medical Device or a highly regulated environment

• Previous supplier engineering experience is advantageous.

• Have knowledge of applicable GMP, FDA and ISO regulations and of other appropriate guidance documents / standards.

• A dynamic team player and can work effectively and proactively on cross-functional teams.

• Good communicator and fluent in English, both in writing and speaking.

Interested candidates should submit an updated CV.

Please click the link below to apply, call Emma on 0214297900 or alternatively send an up to date CV emma.okeeffe@peglobal.net