Medical Devices Jobs

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Clinical Quality Assurance Manager New  

CPL Recruitment - Manchester

qualification (or equivalent experience) · Minimum 5 years’ experience in a GCP environment with demonstrable, working knowledge of GCP practices · Desirable: working knowledge of IVD or medical device Negotiable

from: cpljobs.com - 17 days ago

Senior Supervisor, Maintenance  

Stryker Ireland - Cork

in maintenance of production equipment, ideally within medical device, pharmaceutical, or high-tech manufacturing sectors. Strong understanding of CMMS systems, equipment reliability metrics, and maintenance 12000.0

from: irishjobs.ie - 12 days ago

Project Engineer  

Vantive Health Limited - Mayo

Experience in Construction/Facility systems/Utility systems/Pharmaceutical Processing Experience in commissioning Experience in Pharmaceutical/Medical device What we offer: 25 days Annual Leave with a possible 60000.0

from: irishjobs.ie - 12 days ago

Principal R&D Engineer - SH&A  

Medtronic Vascular Galway UC - Galway

for a dynamic team player that can work effectively and proactively on cross-functional teams. We are looking for an engineer with extensive medical device product development experience and a strong proven track 12000.0

from: irishjobs.ie - 14 days ago

Regulatory Affairs Specialist 2  

Cook Ireland Ltd - Limerick

Overview The Regulatory Affairs Specialist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices 12000.0

from: irishjobs.ie - 19 days ago

Validation Quality Engineer  

Cpl Resources - Cork - Cork (+1 location)

Role Purpose To lead and execute validation activities for medical devices, ensuring full compliance with applicable regulatory standards and quality system requirements. Key Responsibilities Manage 80000.0

from: jobs.ie (+2 sources) - 17 days ago

Lead R&D Engineer, New Product Development  

Hollister Incorporated - F26 F3X5 Ballina, MY, IE

Management experience preferred Length of Experience 8+ years of relevant industry experience preferably in medical devices Specialized skills / Technical knowledge Innovative/Creative Thinker – must

from: Hollister Incorporated - More than 30 days ago

Senior Regulatory Affairs Specialist  

Stryker Ireland - Cork

, Europe and international medical device regulations required. Previous experience with Class II/III medical devices preferred. Previous experience drafting 510(k)s and EU submissions preferred. Experience 12000.0

from: irishjobs.ie - 17 days ago

Medical Scientist  

Bon Secours Health System - Dublin

that ensures compliance with relevant regulations including the Blood Directive 2002/98/EC and the Medical Devices Directives 93/42/EC and 98/79/EC, where applicable. Complete assigned actions, including those 12000.0

from: irishjobs.ie - 16 days ago

Director of Global Quality Management Systems  

Perrigo - D02 TY74 Dublin, IE

Broad expert knowledge of pharmaceutical, medical device, nutritional, API, and cosmetic manufacturing processes. Excellent communication skills (verbal, written, and presentation). Excellent analytical

from: Perrigo - More than 30 days ago


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