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Principal Quality Engineer

Work Your Magic with us! 
 
Ready to explore, break barriers, and discover more? 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. 
•    Controls 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 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!  

Job Requisition ID:  290227
Location:  Carrigtwohill
Career Level:  D - Professional (4-9 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

Notice on Fraudulent Job Offers
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