Principal Quality Engineer

3 weeks ago

Cork, Cork, Ireland Cpl Full time

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We know you've got big plans – so do we
Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics.
Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet.
That`s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
The Role
Reporting to the Membrane QA Manager, the Principal Quality Engineer will be responsible for overseeing the Quality Functions for the Membrane Area.
The Principal Quality Engineer will perform all activities in an efficient and competent manner, with due regard for Safety and Quality, while promoting a positive team environment and a focus on continuous improvement.
Duties:
Supervision, training, and development of assigned Q.A.
staff.
Support colleague engagement model to foster a positive team environment through open communication and feedback.
Lead quality support in Membrane initiatives, ensuring products meet ongoing quality, compliance, and customer requirements.
Oversee the Quality Management System in the Membrane plant to align with site QMS and to ensure effective use, compliance with relevant corporate procedures and quality standards, and continuous improvement.
Support the Membrane Operations team in troubleshooting, process and technology development, and compliance improvement programs.
Facilitate the Membrane Operations continuous improvement process, through implementation of appropriate quality reviews and improvement plans.
Ensure effective and efficient closure of deviations, CAPAs, change controls, audit observations, and customer complaints.
Promote awareness of quality and customer expectations throughout the Membrane Operation.
Ensure compliance with all applicable Environmental, Health and Safety legislation & adherence to procedures for areas of responsibility.
Collaborate with internal cross-functional teams to deliver on operational commitments from a Quality compliance and improvement perspective.
Control the budget allocated to the area.
Other duties as required.
Who You Are
BSc qualified in appropriate scientific discipline
Minimum 5 years relevant experience in a similar role (ideally Pharma/Biopharma)
Excellent communication, collaboration, and leadership skills
Results oriented
Good decision making and problem-solving skills
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