20/05/2024 | Fulltime | Mayo | CV-LibraryImprovements projects. - Write technical documents such as SOP’s. Qualifications/Experience Required - Previous expereince working in a similar role within a pharmaceutical, biotechnology or medical device environment. - Understanding of GMP regulations. - Knowledge of manufacturing operations. - Relevant
Save for later08/05/2024 | Fulltime | Westport | CV-LibraryExperience of working in Biologics, Pharmaceuticals or Medical device industry. - Min of 2 to 5 years’ experience. - Project management experience with proven record - Assured self-starter with proven technical ability - Good communication and interpersonal skills required to operate in a multi-function
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