Job offers for Regulator jobs in Limerick District

15/04/2024 | Fulltime | Limerick | CV-Library | €35 - €48 / Hour And regulatory requirements. You'll be part of a cross-functional collaboration. Working closely with a diverse team of scientists, design engineers, process engineers and other functions to ensure project alignment with goals and milestones. You will also need to complete documentation, maintain comprehensive

15/04/2024 | Fulltime | Limerick | CV-Library | €39 - €52 / Hour Degree in science, engineering or similar Experience managing high value projects on time and to budget Regulatory knowledge, understanding and experience Desirable skills Excellent communication skills Excellent IT skills for project planning Stakeholder management experience The start date is for ASAP

12/04/2024 | Fulltime | Limerick | CV-Library | €39 - €52 / Hour Degree in science, engineering or similar Experience managing high value projects on time and to budget Regulatory knowledge, understanding and experience Desirable skills Excellent communication skills Excellent IT skills for project planning Stakeholder management experience The start date is for ASAP

10/04/2024 | Fulltime | Limerick | CV-Library | €35 - €48 / Hour And regulatory requirements. You'll be part of a cross-functional collaboration. Working closely with a diverse team of scientists, design engineers, process engineers and other functions to ensure project alignment with goals and milestones. You will also need to complete documentation, maintain comprehensive

09/04/2024 | Fulltime | Limerick | CV-LibraryDemonstrable ability to use project management tools. Desirable skills · Experience of working in a medical device, pharmaceutical or processing company. · Experience of interacting with regulatory & clinical scientists · Qualifications/experience in chemistry, polymer science or chemical engineering

27/02/2024 | Fulltime | Limerick | CV-LibraryRequirements · Bachelor's, Master's, or Ph.D. in Biomedical Engineering, Materials Science, Chemistry, or a related field. · Min 2-3 years’ experience in the design & development of Class III medical devices, including familiarity with medical device regulations, and relevant standards (e.g., ISO 13485

16/02/2024 | Fulltime | Limerick | CV-LibraryExperience in an SOP, ISO, or similar regulated environment strongly desired