2026. 01. 18. | Teljes munkaidõ | Gödöllő | 556 GlaxoSmithKline Biologicals Kft.Us achieve our goals Degree in engineering, life sciences, pharmacy or similar technical discipline. Minimum 3 years’ experience in validation or quality roles within a regulated manufacturing environment. Practical knowledge of the validation lifecycle for equipment, utilities, cleaning
Nézze később2026. 01. 18. | Teljes munkaidõ | Gödöllő | 556 GlaxoSmithKline Biologicals Kft.Preparation including MoA, MoP, Core File etc. Preparation of technical documents (Site Master File and Core File) related to the Manufacturing License (ML) of the Site Arrange legalization of GMP and ML certificates for the regulatory submissions Collecting all necessary information from relevant departments
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