documentation Jobs in Basel

pRoche sucht einen GMP-Experten (m/w/d) im Kalibrier-Team am Standort Basel. Sie fungieren als zentrale Schnittstelle für klare, audit-sichere Dokumentation, erstellen SOPs, Arbeitsanweisungen und technische Dokumente und pflegen Stammdaten in CCMS und SAP. /ppSie unterstützen Deviations- und Change-Management, RCA und FMEA und arbeiten eng mit...

h3About this position /h3pAs the Senior Documentation Specialist, you ensure the effective management, quality, completeness, and inspection readiness of essential clinical trial documentation for assigned studies, programmes or documentation activities, including the sponsor TMF and oversight of CRO and laboratory TMFs. You acts as an experienced TMF...

F. Hoffmann-La Roche AG in Basel sucht einen GMP-Experten Kalibrier-Spezialisten (m/w/d) als zentrale Schnittstelle für klare, GMP-konforme Dokumentation. Du bringst komplexe Kalibrierprozesse auf den Punkt und sorgst dafür, dass Audit-nachweisbare Abläufe existieren. Du hast ein abgeschlossenes Studium in Pharmatechnik oder Ingenieurwesen bzw. eine...

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 Documentation Specialist /bto act as a subject matter...

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...

pBachem Holding AG in Basel sucht eine/n Scientific Writer Quality Control zur Erstellung und Pflege analytischer Dokumente im GMP-Umfeld. Sie arbeiten Schnittstellen zwischen Laboren, Projektmanagement, Regulatory und Qualitätssicherung und verbessern kontinuierlich Dokumentenprozesse. /ppSie verfügen über ein naturwissenschaftliches Studium, beherrschen...

pCTC 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. /ppRequired 7–10 years in clinical/nonclinical QA or...

Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement....

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...

ppWählen Sie aus, wie oft (in Tagen) Sie eine Benachrichtigung erhalten möchten: /p h3Senior Documentation Manager (a) (80 -100%) für Engineering Services /h3 pBachem ist ein führendes, innovationsgetriebenes Unternehmen, das sich auf die Entwicklung und Herstellung von Peptiden und Oligonukleotiden spezialisiert hat. Mit einem umfassenden...

Bachem, ein führendes Unternehmen in der Peptid-Chemie, sucht einen Senior Documentation Manager (80-100%). Werde Teil eines dynamischen Teams mit vielen Entwicklungsmöglichkeiten. Aufgaben Verwaltung und Archivierung technischer Dokumentationen in elektronischer und physischer Form Sicherstellung der Einhaltung von GMP- und HSE-Standards sowie...

pSkilled – 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. /ppThe ideal candidate has a Master’s degree in life sciences...

pThe 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...

pbWe are looking for a Technical Regulatory Writer to support the preparation of scientific and regulatory documentation related to pharmaceutical analytical development. /b /p pThe role involves translating analytical data and technical information into clear, accurate, and compliant documentation for pharmaceutical development and regulatory submissions....

h3TRD Composer Technical Service Specialist (m/f/d) /h3pFor our client in the pharmaceutical industry, we are looking for a technically skilled professional with bproven experience in TRD Composer, regulatory documentation and pharmaceutical data management /b. In this role, you will play a key part in the integration and further development of regulatory IT...

pFor our client in the pharmaceutical industry, we are looking for a technically skilled professional with bproven experience in TRD Composer, regulatory documentation and pharmaceutical data management /b. In this role, you will play a key part in the integration and further development of regulatory IT systems, while coordinating data governance activities...

Celonic Group, Basel, is seeking a Technician in Development & Process Optimization to support the development of recombinant protein processes in CHO cultures. You will perform experiments, prepare materials, and collect data under defined timelines, ensuring proper documentation and protocol adherence.Responsibilities include batch documentation, protocol...

pAequor Consulting GmbH is seeking a technically skilled professional with proven experience in TRD Composer, regulatory documentation, and pharmaceutical data management. This role focuses on integrating and advancing regulatory IT systems while coordinating data governance in a highly regulated environment. /ppThe ideal candidate will coordinate data...