Vacatures 21 tot 30 van 40
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Grafton Recruitment - Amsterdam
compliant microbial-based production of recombinant proteins, vaccines, and live microbials as drug substances and products. We are currently seeking a Manager Quality Assurance Operations to join our expanding team.Job Overview The- Volledige vacature bekijken
Trust & Safety Content Moderator and Investigator
Teleperformance - Maastricht
een veiligere online wereld. Sluit je aan bij ons team als Trust & Safety Content Moderator voor Bolt en help ons met het verbeteren van online ervaringen voor miljoenen gebruikers wereldwijd! Wat ga je doen? Als Content- Volledige vacature bekijken
Trust & Safety Content Moderator and Investigator
Teleperformance - Den Helder
een veiligere online wereld. Sluit je aan bij ons team als Trust & Safety Content Moderator voor Bolt en help ons met het verbeteren van online ervaringen voor miljoenen gebruikers wereldwijd! Wat ga je doen? Als Content- Volledige vacature bekijken
Synthon - Nijmegen
Research and Development & Drug Product Manufacturing Carrer de Castelló, 1, 08830 Sant Boi de Llobregat Barcelona, Spain Job details At Synthon you will have a great experience, in an excellent work environment, and- Preview - Opslaan
Warehouse Operator (temporary)
Synthon - Nijmegen
Research and Development & Drug Product Manufacturing Carrer de Castelló, 1, 08830 Sant Boi de Llobregat Barcelona, Spain Job details At Synthon you will have a great experience, in an excellent work environment, and- Preview - Opslaan
Moldmaker Peachtree City (GA), USA
Igs Gebojagema - Eindhoven
requirements Technical Education 8 – 10 years of relevant work experience Reading technical drawings General Safety Requirements MS Office Competencies we are looking for Collaboration Quality- Preview - Opslaan
Venlo bij IQVIA via Jobsonline - Venlo
week and is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety - Preview - Opslaan
Ede bij IQVIA via Jobsonline - Ede
week and is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety - Preview - Opslaan
Oxfordcorp
data coding and safety reviews as needed; Contribute towards process improvement, data standards and efficiency gaining initiatives within data management working with data management leadership as needed; Be60+ dagen geleden - Preview - Opslaan
Oxfordcorp
image handling; Be responsible for coordinating with Medical Affairs organization to facilitate data coding and safety reviews as needed; Contribute towards process improvement, data standards and efficiency gaining60+ dagen geleden - Preview - Opslaan
Oxfordcorp
Specialist supports drug label preparation and approval (as local label representative) for studies in collaboration with local Regulatory/Quality department, as required The Study Start-Up Specialist liaises and collaborates60+ dagen geleden - Preview - Opslaan
Empower your career - a female perspective
Hyphen Projects - Utrecht
are making waves in the Life Sciences! Speakers Liesbeth Hof | Sr Director Project Management Office | AM-Pharma Liesbeth Hof has a Master in Medical Biology with over 20 years of international experiences in the- Preview - Opslaan
(Junior) Clinical Trial Assistant EN or FR/EN or FR/EN)
Oxfordcorp
Do you actively want to contribute supporting drug development, in one of the biggest biotech companies, with an amazing pipeline? Then this job as Clinical Trial Assistant might be for you ! Job Description As a60+ dagen geleden - Preview - Opslaan