Hays AG
QA Documentation Specialist (m/f/d)
Publiziert am: 10.09.25 | Neuenburg | Vollzeit
Jetzt bewerben- Own and maintain documentation systems and archiving processes
- Provide user support and training on documentation tools (e.g., Veeva Vault)
- Create, update, and manage controlled documents
- Collaborate On site and global initiatives to improve quality systems
- Support audits, inspections, and quality metrics reporting.
- Degree in life sciences or related field
- Experience in the (bio)pharma industry
- Knowledge of GMP, GDDP, and regulatory standards
- Fluent in French and English
- Proficient in Microsoft Office and document management systems.
- Good infrastructure
- A very renowned company
Ihr Kontakt
Ansprechpartner
Nadia Moumni
Referenznummer
838947/1
Kontakt aufnehmen
E-Mail: nadia.moumni@hays.ch
Anstellungsart
Freiberuflich für ein Projekt
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Willy-Brandt-Platz 1-3
68161 Mannheim
