Vacatures 91 tot 100 van 109 (ontdubbeld 105)
ads
- Volledige vacature bekijken
- Volledige vacature bekijken
- Volledige vacature bekijken
BAM Bouw en Techniek - Amsterdam
afhankelijk van je project. Taken zijn onder andere: Review van aangeleverde ontwerpen (afhankelijk van project VO;DO;TO) DO-ontwerpen doorontwerpen naar technisch ontwerp en vervolgens naar UO (UitvoeringsOntwerp)-tekeningen. Zorgen- Volledige vacature bekijken
Lead Engineer Werktuigbouwkunde
BAM Bouw en Techniek - Amsterdam
zowel op land- als airside, afhankelijk van het project. Taken zijn onder andere Review van aangeleverde ontwerpen ( afhankelijk van project VO;DO;TO), DO- ontwerpen doorontwerpen naar Technisch Ontwerp en vervolgens omzetten- Volledige vacature bekijken
Lead Engineer Werktuigbouwkunde
BAM Bouw en Techniek - Schiphol
zowel op land- als airside, afhankelijk van het project. Taken zijn onder andere Review van aangeleverde ontwerpen ( afhankelijk van project VO;DO;TO), DO- ontwerpen doorontwerpen naar Technisch Ontwerp en vervolgens omzetten- Volledige vacature bekijken
Finnish speakers wanted to become a video content an...
Working Adventures - Amsterdam
Video Content Analyst Lisbon, Portugal Finnish Tämä avoin paikka on vanhentunut Etsi muita avoimia työpaikkoja Embark on a new adventure as a Video Content Analyst in Lisbon and work for one of the most wellDigital Marketing Potential Kawasaki Motors Benelux
Nieuwsmotor.nl - Hoofddorp
activities (within the digital marketing budget); Initiate, plan and produce new (unique) content for digital activities and support the dealer network in their digital activities; Maintain, manage and develop the Kawasaki- Preview
Freelance Principal Medical Writer Remote Life Sciences
Yacht via Talent - Amsterdam
process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content fromFreelance Principal Medical Writer Remote Life Sciences
Yacht via Talent - Amsterdam
process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content fromFreelance Principal Medical Writer remote Life Sciences
Yacht via Talent - Amsterdam
process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content fromFreelance Principal Medical Writer remote Life Sciences
Yacht via Talent - Amsterdam
critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts.Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content from sourceFreelance Principal Medical Writer remote Life Sciences
Yacht via Talent - Amsterdam
process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content fromFreelance Principal Medical Writer remote Life Sciences
Yacht via Talent - Amsterdam
process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content fromFreelance Principal Medical Writer remote Life Sciences
Yacht via Talent - Amsterdam
process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content fromFreelance Principal Medical Writer remote Life Sciences
Yacht via Talent - Amsterdam
process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content from