veeva

Position Overview Slipstream Europe is seeking an experience Project Manager, CRM to lead client engagements involving Veeva CRM and related CRM platform implementations. This role requires a seasoned project leader who can independently manage end-to-end delivery of CRM implementations and enhancements for life sciences clients, balancing scope, timeline,...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer...

ppVeeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. /p pAt the heart of Veeva are our values: Do the Right Thing,...

Octapharma is seeking a Group Senior Analyst Quality Applications in Lachen, CH, to serve as a subject matter expert for global Quality applications such as Veeva QualityDocs, Veeva QMS, and LIMS. You will own configuration, validation readiness, and release coordination in a GxP environment.The ideal candidate has 5–7 years of hands-on Quality apps...

pVeeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. /p pAt the heart of Veeva are our values: Do the Right Thing,...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer...

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...

Octapharma AG, headquartered in Lachen, Switzerland, seeks a Group Senior Analyst Quality Applications to drive global quality systems (Veeva QualityDocs, Veeva QMS, LIMS) and ensure compliant, user-centered solutions. You will own configuration, validation readiness, and change management within a GxP environment.The role requires 5–7 years’ hands-on...

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,...

Veeva Systems is seeking a European Strategy role within Veeva Batch Release to shape how the market understands batch-disposition and release processes. You will work with customers, partners, and Veeva teams to turn regulatory manufacturing knowledge into practical software, services, and field strategies.This senior, customer-facing role requires deep...

Gi Group (United Kingdom) cherche un(e) Compliance Specialist pour renforcer les équipes qualité sur site à Nyon, Suisse, ASAP. Vous assurerez la conformité GMP et gérerez les déviations, CAPA et investigations.Vous documenterez les déviations dans Veeva, suivrez les CAPA jusqu’à clôture et participerez à l’amélioration continue des processus...

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 -...

pVeeva Systems is seeking a European Strategy role within Veeva Batch Release to shape how the market understands batch-disposition and release processes. You will work with customers, partners, and Veeva teams to turn regulatory manufacturing knowledge into practical software, services, and field strategies. /ppThis senior, customer-facing role requires...

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...

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...

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...

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...