veeva systems

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...

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,...

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,...

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...

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,...

Zur Unterstützung der Weiterentwicklung unserer Quality-Organisation suchen wir für den Bereich QA Compliance & Systems eine engagierte und erfahrene Persönlichkeit als Manager QA – Quality Management Systems (QMS) (a), 100 %. In dieser Funktion übernehmen Sie Verantwortung für die Weiterentwicklung und Harmonisierung unserer...

Wählen Sie aus, wie oft (in Tagen) Sie eine Benachrichtigung erhalten möchten:Bachem ist ein führendes, innovationsgetriebenes Unternehmen, das sich auf die Entwicklung und Herstellung von Peptiden und Oligonukleotiden spezialisiert hat. Mit einem umfassenden Dienstleistungsangebot bietet Bachem pharmazeutischen und biotechnologischen Unternehmen weltweit...

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...

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...

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...

Travere Therapeutics in Switzerland is hiring a Senior Specialist, Regulatory Affairs (EU/RoW) to support the preparation, submission and maintenance of regulatory applications, including CTA submissions and post-authorization activities.You will work with regulatory leads, coordinate with external contractors, maintain document management systems such as...

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 -...

BeiGene, Ltd. is seeking an Associate Director, Good Clinical Practice (GCP) Audits and Inspections to lead GCP audits, support regulatory inspection readiness, and provide quality oversight across clinical development programs.The role partners with cross-functional teams to ensure compliance with ICH GCP and global regulations. You will oversee vendor...

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....

Experis is seeking a Quality Assurance Associate for the Solothurn site to strengthen the Quality Management System and support core quality activities. You will collaborate with site and global functions to ensure compliance and timely action, including audits, governance, and CAPAs, while maintaining documentation in systems like TrackWise, Veeva, and...

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...

Travere Therapeutics in Switzerland is hiring a Senior Specialist, Regulatory Affairs (EU/RoW) to support the preparation, submission and maintenance of regulatory applications, including CTA submissions and post-authorization activities.You will work with regulatory leads, coordinate with external contractors, maintain document management systems such as...

Veeva Systems is seeking an Account Partner for its Quality Cloud to drive growth across the Life Sciences SMB markets in the DACH region from Basel, Switzerland. You will generate opportunities, win new business, and build strategic customer relationships while helping organisations modernise operations through cloud technology.A strong understanding of the...

pEraneos is looking for a Digital Transformation Leader in Zürich, Switzerland. This role involves driving digital transformations in Clinical and Pharmacovigilance through innovative solutions and effective project management. /ppYou will lead project teams, guide clients in digital tool adoption, and provide strategic insights on digital initiatives....