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Regulatory Affairs Jobs in Galway

1 - 15 of 17
1 - 15 of 17
Search Results - Regulatory Affairs Jobs in Galway
Life Science Recruitment-Galway
Our client a growing medical device organisation currently seeks a Senior Regulatory Affairs Specialist to join their team. The Senior Regulatory Affairs Specialist will be responsible for all regulatory activities including product certification...
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appcast.io -
Reperio Human Capital Ltd-Galway
Quality, or a related discipline 3-7 years in QA or manufacturing quality within a regulated industry Strong knowledge of ISO 13485, FDA QSR, and process validation Experience supporting regulatory audits or working with Regulatory Affairs teams...
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Wallace Myers International-Galway
Job Title: Director of Quality Assurance & Regulatory Affairs Location: Galway, Ireland (or hybrid/remote as applicable) Department: Quality & Regulatory Reports To: Chief Operating Officer / CEO Role Overview We are seeking a highly experienced...
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Accpro-Galway
change approval. Interface with Regulatory Affairs to ensure information is clearly presented to minimize Regulatory Agency questions. Contribute to establishing strong working cross functional relationships across the organization and with partners...
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Wallace Myers International-Galway
Job Title: Director of Quality Assurance & Regulatory Affairs Location: Galway, Ireland (or hybrid/remote as applicable) Department: Quality & Regulatory Reports To: Chief Operating Officer / CEO Role Overview We are seeking a highly experienced...
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CareerWise Recruitment-Galway
in the compilation of design verification and shelf-life data for regulatory submissions to support design change approval. Interface with Regulatory Affairs to ensure information is clearly presented to minimize Regulatory Agency questions. Contribute...
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Life Science Recruitment-Galway
QMS) to ensure compliance with ISO 13485, FDA 21 CFR 820, MDR, and other applicable standards and regulations.  •  Partner closely with Operations, R&D, Regulatory Affairs, and Commercial teams to support product development, manufacturing, and market...
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Accpro-Galway
will participate in the compilation of design verification and shelf life data for regulatory submissions to support design change approval. Interface with Regulatory Affairs to ensure information is clearly presented to minimize Regulatory Agency questions...
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Boston Scientific Gruppe-Galway
management in an Operations or New Product Development environment  •  Strong experience in project managing larger-scale / complex projects involving multiple functions (e.g. Divisional R&D, Program Management, Regulatory Affairs, Design Assurance, Process...
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appcast.io -
CPL-Galway
and shelf-life data for regulatory submissions.  •  Interface with Regulatory Affairs to present data clearly and minimize questions from regulatory agencies.  •  Build strong working relationships across R&D, Regulatory Affairs, Quality, and Manufacturing teams...
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cpl.com -
Collins McNicholas Recruitment-Galway
and shelf life data for regulatory submissions.  •  Partner with Regulatory Affairs to ensure clear, accurate, and complete information is presented in submissions to minimize regulatory queries.  •  Establish and maintain strong cross-functional relationships...
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appcast.io -
Galway
will participate in the compilation of design verification and shelf-life data for regulatory submissions to support design change approval.  •  Interface with Regulatory Affairs to ensure information is clearly presented to minimize Regulatory Agency questions...
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careerwise.ie -
Sigmar Recruitment-Galway
with Regulatory Affairs to ensure clear presentation of information, minimizing Regulatory Agency queries. Establish strong cross-functional relationships within the organization and with external partners in a complex technical environment. Maintain up-to-date...
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Collins McNicholas Recruitment-Galway
for products / programs of moderate risk. Requirements:  •  Minimum of 7-10 years’ experience in a Quality role. 2 – 5+ years regulatory affairs experience or related experience in medical device industry and/or Pharmaceuticals is required.  •  Working knowledge...
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appcast.io -
Galway
will participate in the compilation of design verification and shelf-life data for regulatory submissions to support design change approval.  •  Interface with Regulatory Affairs to ensure information is clearly presented to minimize Regulatory Agency questions...
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careerwise.ie -
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