24/05/2024 | Fulltime | | Netherlands | CV-Library | €64,743 - €73,375 / Year Authorities, notified body, EU expert panel, and FDA, you will oversee the preparation and follow-up of FDA pre submissions, CE-mark dossiers, and other regulatory submissions, taking ownership of these critical processes. Senior Regulatory Affairs Specialist Responsibilities Spearhead the development
Save for later21/05/2024 | Fulltime | | Netherlands | CV-Library | €75,000 - €90,000 / Year Planning and scheduling and/or themed entertainment planning/coordination experience, which includes a combination of Experience in Critical Path Method scheduling experience utilizing scheduling software. Experience in construction, production, and/or design experience. Good understanding of practical
Save for later01/05/2024 | Fulltime | | Netherlands | CV-LibraryThey have an excellent track record of health and safety performance, and this role is critical to ensure this is not only maintained but continually improved and developed. This role has responsibility for a major Data Centre project in Amsterdam. Candidates must have the right to work in the Netherlands
Save for later28/03/2024 | Fulltime | | Netherlands | CV-Library | €42,800 - €46,900 / Year A full, clean driving license with the willingness to undertake extensive country-wide travel and overnight stays where required. - A Degree in a business management field or the equivalent would be a bonus but is not critical. Benefits - 25 days statutory holidays per annum - bank holidays - Enhanced
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