documentation Jobs in Basel

Herzog & de Meuron Basel Ltd sucht eine:n Dokumentationsmanager:in zur Unterstützung ihrer Architekt:innen in der Dokumentation und Archivierung von Projekten. Sie werden für die langfristige Erhaltung von Dokumenten und digitalen Inhalten verantwortlich sein und begleiten sämtliche Projektphasen.Erforderlich sind ein starkes Interesse an Architektur,...

Herzog & de Meuron ist ein internationales Architekturbüro mit Sitz in Basel, Schweiz. Das Büro wurde 1978 gegründet und wird von den beiden Gründern, zusammen mit den Partnern und dem CEO geleitet. Heute engagiert sich ein internationales Team von über 500 Mitarbeitern an einer Vielzahl von Projekten in Europa, Amerika und Asien. Der Hauptsitz in Basel...

Medical Writer Documentation Specialist - 7103Our 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 Medical Writer Documentation Specialist to act as a subject matter expert for...

UBS Basel seeks a specialist to produce UCITS KIIDs and PRIIP KIDs for UBS funds and third-party client funds. You will oversee documentation from data gathering to final production, coordinating with Product Managers and Client Relationship Managers in Basel.The role requires a degree or equivalent experience in fund management or regulatory affairs, strong...

pOur client is seeking an experienced Senior Documentation Quality Specialist to act as a subject matter expert for the quality of clinical, nonclinical, and regulatory documentation. The role ensures that key deliverables are clear, accurate, consistent, compliant, and submission-ready, supporting development programmes, health authority interactions, and...

pCTC Resourcing Solutions AG in Basel area is seeking an experienced Medical Writer Documentation Specialist for a 2-year contract. You will ensure clinical, nonclinical, and regulatory documents are clear, accurate, compliant, and submission-ready to support global regulatory submissions. /ppThe role requires a Master’s degree, at least 10 years in...

pbMedical Writer Documentation Specialist – 7103 /b /ppOur 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 bMedical Writer /b bDocumentation Specialist /b to act as a subject...

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...

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....

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...

The Senior Documentation Quality Specialist acts as an enterprise Subject Matter Expert (SME), ensuring maximum rigor across clinical, nonclinical, and regulatory documentation. This position is accountable for the clarity, precision, structural consistency, and regulatory compliance of critical assets across global development programs, health authority...

CTC Resourcing Solutions seeks a Medical Writer Documentation Specialist for a 2-year Basel-area contract. You will act as a subject matter expert ensuring clinical, nonclinical, and regulatory documents are accurate, compliant, and submission-ready across NDA, MAA, CSR, DSUR, and IND dossiers.Required 7–10 years in clinical/nonclinical QA or regulatory...

Skilled – Recruitment Solutions GmbH is seeking a Senior Documentation Quality Specialist to ensure rigor across clinical, nonclinical, and regulatory documents within global development programs. The role emphasizes clarity, regulatory compliance, and governance of templates and standards.The ideal candidate has a Master’s degree in life sciences with...

Techfirm Engineering is seeking a QA Specialist / QMS associate (m/w/d) to reinforce our Industrial Services team in Switzerland. Based in Basel, you will focus on GMP documentation review, quality approvals, QMS activities, and audit support.Ideal candidates have initial GMP-regulated pharmaceutical experience and at least 1 year in Quality Assurance/QMS,...

Roche sucht eine engagierte Lernende im Bereich Information & Dokumentation in Basel. Die Ausbildung dauert 3 Jahre und bereitet dich professionell auf die Arbeitswelt vor. Du lernst Dokumentenverwaltung, Datenbanken, und den Umgang mit historischen Materialien in einer internationalen Umgebung.Nach der Ausbildung gibt es Weiterbildungswege an...

Medical Writer Documentation Specialist – 7103Our 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 Medical Writer Documentation Specialist to act as a subject matter expert for...

CTC Resourcing Solutions AG in Basel area is seeking an experienced Medical Writer Documentation Specialist for a 2-year contract. You will ensure clinical, nonclinical, and regulatory documents are clear, accurate, compliant, and submission-ready to support global regulatory submissions.The role requires a Master’s degree, at least 10 years in...

pFlexsis is seeking an experienced Senior Documentation Quality Specialist to ensure the highest quality of clinical, nonclinical, and regulatory documentation. You will act as a subject matter expert, guiding authors and cross-functional partners to deliver accurate, compliant, and submission-ready documents for health authority interactions and global...

CTC Resourcing Solutions AG in Basel area is seeking an experienced Medical Writer Documentation Specialist for a 2-year contract. You will ensure clinical, nonclinical, and regulatory documents are clear, accurate, compliant, and submission-ready to support global regulatory submissions.The role requires a Master’s degree, at least 10 years in...

Medical Writer Documentation Specialist – 7103Our 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 Medical Writer Documentation Specialist to act as a subject matter expert for...