documentation

Bien-Air Dental SA offre un stage de 6 mois dans le service Affaires Réglementaires à Bienne. Vous participerez activement à la mise à jour des notices d’utilisation de dispositifs médicaux, en conformité avec les normes et règlements applicables, et assurerez la traçabilité des versions.Vous travaillerez en étroite collaboration avec les...

pCreate and manage high-quality technical documentation for advanced unmanned helicopter systems, ensuring clarity, compliance, and effective knowledge transfer across engineering and operational environments. /p h3Your Role Responsibilities /h3 ul lipDevelop, maintain, and manage technical documentation including user manuals, maintenance guides,...

ppbSenior Regulatory Affairs Documentation Specialist – 7103 /b /p pOur client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for an experienced bSenior Regulatory Affairs Documentation Specialist /b...

pBachem in Vionnaz, Switzerland, is seeking a Technical Author to join our TechOps team on a full-time basis. You will create and maintain GMP manufacturing documentation, support technology transfer projects, and translate process knowledge into compliant, manufacturing-ready records. /ppYou will work closely with Process Scientists, laboratories,...

pXapply seeks a Stability Documentation Manager - RD, based in Switzerland, to own product shelf-life validation and the essential technical documentation for every SKU. You will lead stability testing, validate analytical methods, and collaborate with external labs in a fully remote, high-trust environment. /ppYou will partner with Quality, Operations, and...

Senior Regulatory Affairs Documentation Specialist – 7103 Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for an experienced Senior Regulatory Affairs Documentation Specialist to act as a...

pApple Inc. is seeking a Content Engineering Author for Developer Publications to create and refine developer documentation, sample code, and API references. You will work with editors, engineers, and designers to produce clear technical content that educates millions of developers about Apple platforms. /ppThe role emphasizes turning complex topics into...

ph3IMS Documentation Manager (w/m/d) /h3 pBegeistern Sie sich für Qualitätsmanagement, Prozessexzellenz und ein wirkungsvolles Dokumentationsmanagement? In dieser Schlüsselfunktion haben Sie die Möglichkeit, unser globales Integrated Management System (IMS) aktiv mitzugestalten und weiterzuentwickeln. Sie treiben die Harmonisierung unserer Prozesse...

Senior Regulatory Affairs Documentation Specialist – 7103 Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for an experienced Senior Regulatory Affairs Documentation Specialist to act as a...

pSchurter AG seeks a senior quality management professional to lead the global Integrated Management System and drive documentation governance across all sites. You will coordinate certification activities and ensure readiness while promoting process harmonization and operational excellence. /ppRequired is a technical degree with extensive serial production...

ppAre you passionate about quality management, process excellence and effective documentation? In this key role, you will have the opportunity to shape and further develop our global Integrated Management System (IMS), drive process harmonization and ensure effective document governance across all SCHURTER sites. /p h3Your Responsibilities /h3 ul liLead and...

pIBSA Institut Biochimique SA cerca un/una Clinical Research Officer con pluriennale esperienza, preferibilmente in CRO o industria farmaceutica, da inserire nel team Clinical Research. La risorsa supporterà il CRM nelle attività operative e amministrative degli studi clinici, contribuendo all'avvio, svolgimento e chiusura conformemente alle SOP interne e...

pBachem SA in Vionnaz, Switzerland, seeks a Technical Author to join the TechOps team at 1895 Vionnaz (VS). You will create and maintain GMP manufacturing documentation, support technology transfer and new product introductions, and digitalize manufacturing records. /ppApplicants should hold a Master’s degree or PhD in Chemistry or related field, with...

pPILATUS Flugzeugwerke AG in Switzerland is seeking a documentation specialist to create and maintain 2D and 3D Illustrated Parts Catalog (IPC/IPD) in line with project schedules. You will work with engineering data and CAD to ensure accurate IPC/IPD. /ppYou will compile technical documentation according to ASD S1000D, review and prepare content for...

Proclinical Staffing sucht einen Verpackungsbediener zur manuellen Etikettierung und Verpackung von Medikamenten in klinischen Studien. Sie arbeiten gemäß GMP-, Sicherheits- und Umweltvorschriften und sichern saubere, ordentliche Arbeitsbereiche.Zu Ihren Aufgaben gehören Dokumentation, Qualitätsprüfungen und Zusammenarbeit mit anderen Abteilungen....

Dynafer SA recherche un rédacteur technique à La Chaux-de-Fonds pour réaliser l’analyse documentaire, l’inventaire des documents et la définition des modèles rédactionnels. Vous assurerez l’écriture et la mise à jour des instructions de travail en respect des standards définis.Ce poste nécessite une maîtrise des outils MS Office, une...

Main responsibilities Execute data remediation strategies by identifying, analysing, and resolving data issues within the banking systems. Collaborate with IT teams to develop and implement data cleansing and data migration strategies. Collaborate with various teams to develop and implement data quality improvement initiatives. Conduct detailed data...

CTC Resourcing Solutions is seeking a QA Specialist to support GMP documentation review, QA activities for IMPs, and coordination with CMOs. The role focuses on ensuring documentation completeness, inspection readiness, and timely QA operations.The ideal candidate will have a Life Sciences/Pharmacy degree and 1–3 years of GMP experience, with strong...

CTC Resourcing Solutions is seeking a QA Specialist to support GMP documentation review, QA activities for IMPs, and coordination with CMOs. The role focuses on ensuring documentation completeness, inspection readiness, and timely QA operations.The ideal candidate will have a Life Sciences/Pharmacy degree and 1–3 years of GMP experience, with strong...

Octapharma is seeking a Clinical Trial Documentation Specialist to set up and maintain TMFs and ISFs, while supporting the clinical team with regulatory submissions and trial documentation across international trials. You will track essential documents, ensure audit readiness, and act as the central point of contact for trial documentation.The role requires...