BD Medical is a leading global medical technology company. Established in 1897, BD has grown into a multinational Fortune 500 enterprise. With a philosophy of social awareness and continuous improvement, BD has become a world leader in the design, manufacture and sale of quality medical supplies, plus devices and diagnostic systems for use by health care professionals, medical research institutions, industry and the general public.
Supported by over 30,000 people world-wide, in more than 80 facilities in 40 countries, our business is driving towards one single vision – to help all people live healthy lives.
BD Medical have been established in Ireland for over 40 years, with manufacturing plants in Drogheda and Dun Laoghaire, supplying diabetes healthcare products to a worldwide market.
Also based in the Dun Laoghaire office are members of Regional and Global Sales, Contract Manufacturing and Company Procurement Teams alongside Benex Ltd., which is a member of the BD group. Benex Ltd. operates as a European Trading Centre for group activities, providing accounting & financial services for BD’s European central warehousing operations.
Quality Systems Engineer is responsible for implementation and maintenance of the Company’s Quality Management Systems to ensure alignment with current local, unit and federal regulations. This role also involves active participation in both internal and external audits.
The Supplier Development Manager personally leads commercial and quality systems assessments for key suppliers, with particular focus on identification and quantification of opportunities for joint improvement activities.
We are seeking qualified candidate to support all aspects of the quality system for the Limerick facility.
We are seeking candidates for fixed-term maternity cover contract.
The Training/CI Assistant will liaise with the Training Co-ordinator to develop, deliver and monitor training to meet both quality and manufacturing needs. He/she will work with the CI lead in the development and implementation of the site CI plan.
• Reporting to the Quality Engineering Manager, duties will include active participation in non-conformance investigations and lot disposition decisions, application of SPC to current production processes and liaison with key customers.
Provides technical leadership, daily oversight, and subject matter expertise needed to manage the microbiology laboratory function and team
The role provides practical, hands on product in servicing to the sales team and their customers at a tactical level covering the MPS business portfolio with focus on Posiflush , Injection safety range, Venflon Pro safety and Nexiva.
Duties will include management and execution of process validation studies, active participation in non-conformance investigation, process improvement projects, project management, application of SPC to current production processes and liaison with key customers.