veeva Jobs in Basel

Work Selection AG sucht in Basel eine Regulatory Specialist (CMC) für ein 12-monatiges Projekt mit Roche-Partnern. Sie unterstützen regulatorische Aktivitäten im kommerziellen Bereich und Post-Marketing-Remediation, arbeiten mit Veeva RIM und liefern regulatorische Expertise über den Produktlebenszyklus hinweg.Sie verfügen über relevante...

Actalent in the Basel area seeks a Regulatory Specialist (CMC) with 4+ years of experience to support lifecycle management, regulatory maintenance, and post-approval submissions for commercial pharmaceutical products. The role emphasizes change controls, remediation, data management in Veeva and Veeva RIM and collaboration across functions.You will serve as...

Our client is a leading international pharmaceutical company with a strong portfolio of innovative and established products. To support ongoing lifecycle and remediation activities, we are seeking Regulatory Specialists (CMC) with experience supporting commercial products and post-approval regulatory processes.This role focuses on lifecycle management,...

Regulatory Specialist - Clinical or Early-Stage Development Regulatory Specialist - Clinical / Early-Stage Development (CMC Focus) : CMC / IMPs / Clinical TrialApplications (CTAs) / Change Control / Deviation Management /Change controls / CMC regulatory / VeevaDocument Management / Post-Marketing / Remediation/ English / Deutsch Regulatory Specialist -...

Bachem 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.Sie verfügen über ein naturwissenschaftliches Studium, beherrschen...

Roche sucht eine Logistics & Warehouse Compliance Specialist in Basel/Kaiseraugst, der GxP-Compliance sicherstellt und eng mit QA, Business Circles sowie Partnern zusammenarbeitet.Sie haben eine Ausbildung oder Bachelor/Master im Pharma- oder Logistikbereich, 3–5 Jahre GMP/GDP-Erfahrung und Erfahrung mit GxP-Abweichungen/Change-Management (Veeva). Start...

Work Selection AG in Basel sucht per sofort einen Logistics & Warehouse Compliance Specialist für einen temporären Einsatz von 1 Jahr mit Option auf Verlängerung. Sie arbeiten eigenverantwortlich im GMP/GDP-Umfeld und prüfen Transportdaten sowie Wareneingänge.Zu Ihren Aufgaben gehören das Change-Management in GxP-Prozessen, die Dokumentenbearbeitung in...

Work Selection AG sucht Regulatory Specialist (CMC) für Roche Basel in Basel für eine 12‑monatige befristete Anstellung. Sie arbeiten im PTR‑Team und unterstützen technische regulatorische Aktivitäten über den Produktlebenszyklus hinweg.Schwerpunkt liegt auf post‑approval Regulatory Maintenance, Change Controls, Regulatory Deviations,...

Gi Life Sciences Stein in Basel bietet eine Position als Logistiker mit GMP-Erfahrung. Sie prüfen Transporttemperaturen, überwachen Wareneingänge und unterstützen GxP-Fragestellungen im Logistic Solutions Umfeld.Sie arbeiten in einem crossfunktionalen Team, bringen Deutsch C1 und Englisch B2 mit, und übernehmen Verantwortung für Abweichungen in Veeva...

In the position of Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR), you will be accountable for handling all Health Authority interactions pertaining to CMC Information (for example in an IND, IMPD and NDA/BLA/MAA filings), as well as informational and/or pre-submission meetings with global Health Authorities, partners and industry experts....

Gi Life Sciences Basel sucht eine/n Logistics & Warehouse Compliance Spezialist:in zur Sicherstellung von GxP-Compliance im Bereich Logistic Solutions in Basel und Kaiseraugst. Sie arbeiten eng mit Qualitätsfunktionen, Business Circles und externen Partnern zusammen.Zu Ihren Aufgaben gehören das Auslesen von Transport-Temperaturdaten, Prüfung von...

BeOne is seeking an Associate Director, GCP Audits and Inspections within R&D Quality & GxP Auditing to lead and execute GCP audits, support regulatory inspection readiness, and provide quality oversight across clinical development programs.The role collaborates with cross-functional stakeholders and utilizes Veeva Vault to plan, document, and track audit...

Roche Basel seeks a Regulatory Specialist (CMC) focused on Clinical/Early-Stage Development to lead global technical regulatory submissions (IND/IMPD/CTAs) and manage change controls in Veeva environments. The role requires collaboration with PTR, affiliates, and external partners across the product lifecycle.The ideal candidate has a Bachelor in a relevant...

Actalent is seeking a Regulatory Specialist (CMC) to drive global regulatory submissions for clinical-stage products and to support IMPDs, CTAs and related CMC documentation. You will liaise with cross-functional teams across development, manufacturing and quality to ensure alignment with Health Authority expectations.The role requires 3–4+ years in CMC...

Gi Group is seeking a Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR) to lead global regulatory submissions and manage CMC information for IND, IMPD, and NDA/BLA/MAA filings. The role collaborates with affiliates, policy teams, and partners on early clinical stage programs and IMPD submissions.The ideal candidate has 3–4 years of CMC...

Our client is a global leader in the pharmaceutical industry, committed to advancing science and delivering innovative therapies to patients worldwide. To support ongoing clinical development activities, we are looking for a Regulatory Specialist (CMC) with experience in early-stage development and clinical regulatory submissions.In this role, you will...

Veeva Systems is seeking an Account Partner for Quality Cloud to drive growth across Life Sciences small and medium biotechs in Switzerland. You will generate opportunities, win new business, and build strategic customer relationships while helping organisations modernise operations with innovative cloud technology.The role requires 5+ years in...

Manpower Switzerland seeks an experienced Regulatory Specialist (CMC) to support lifecycle management, regulatory compliance, and post-approval activities for commercial pharmaceutical products. The role emphasizes managing change controls, deviations, and remediation within global systems.The ideal candidate will have a Life Sciences background and 3–4...

Work Selection AGAs a first-tier supplier to our renowned business partner F. Hoffmann-La Roche Ltd. in Basel, we are currently looking for a motivated and dedicated Regulatory Specialist ? Commercial / Post-Marketing & Remediation (CMC) for a temporary assignment of 12 months.A healthier future. It's what drives us to innovate. To continuously advance...

CTC Resourcing Solutions is seeking a hands-on Data Manager to support Clinical Data Management activities in Basel. The role requires immediate contribution to DMP preparation, data cleaning, QA/RA tasks, and data transfer specifications, on a 24-month contract based in the Basel area.Responsibilities include eCRF design using Medidata Rave, Veeva EDC, and...