Manager Technical Product Management (m/w)

Actelion Pharmaceuticals Ltd; Allschwil; Vor Ort; CHF 150.000 - 190.000; Vollzeit

Zusammenfassung

Actelion Pharmaceuticals Ltd seeks an experienced Manager of Technical Product Management to advance our Pharmacovigilance technology landscape. You will own PV case processing and safety platforms, driving innovation and regulatory compliance across global systems.

You will partner with Safety, Regulatory, and IT teams to scale platforms, lead end-to-end delivery, and improve data intake, analytics, and automation using LSMV, ReporterX, XDI, and RxLogix.

Qualifikationen

• Bachelor’s degree in IT, life sciences, or a related field.
• 5–8+ years of experience in product management or IT application ownership in Pharmacovigilance.
• Hands-on with LSMV, ReporterX/XDI, RxLogix for data intake and integration.
• Experience in GxP-regulated environments and PV compliance requirements.
• Strong communication and leadership skills and stakeholder management.

Aufgaben

• Own and execute the PV case processing product roadmap and safety platforms.
• Lead Agile delivery by prioritizing backlog and end-to-end lifecycle.
• Oversee ICSR case processing from intake to regulatory submission.
• Act as product/IT lead for ArisGlobal LSMV and manage ReporterX/XDI.
• Enable integration with RxLogix to support signal detection and analytics.
• Promote automation and AI to improve data quality and throughput.
• Ensure PV regulatory compliance and audit readiness.
• Monitor system performance, SLAs, and data quality KPIs.
• Interface IT with Pharmacovigilance teams to align priorities.
• Collaborate with vendors on strategy, upgrades, and innovation.
• Optimize cost and system utilization, build a high-performing team.

Kenntnisse

Communication

Leadership

Stakeholder management

Agile methodologies

Ausbildung

Bachelor’s degree in IT/Life Sciences

Tools

ArisGlobal LifeSphere MultiVigilance (LSMV)

ReporterX

XDI

RxLogix (RxL) platform

Jobbeschreibung

Manager Technical Product Management (m/w)

Actelion Pharmaceuticals Ltd Vacant since : 07.08.2026 Number of jobs : 1 4123 Allschwil (BL) 100% By agreement Permanent

We are seeking an experienced Manager who can evolve our Pharmacovigilance (PV) technology landscape, with a strong focus on case processing systems and operational excellence.

This role will partner closely with Safety, Regulatory, and IT teams to drive innovation, scale, and compliance across global PV platforms. The ideal candidate brings deep expertise in ICSR case processing workflows and hands-on experience with ArisGlobal LifeSphere MultiVigilance (LSMV), ReporterX, XDI, and RxLogix (RxL).

Key Responsibilities

• Own and execute the product roadmap for Pharmacovigilance (PV) case processing and safety platforms, translating business needs into scalable, compliant technology solutions
• Lead Agile delivery by prioritizing backlog and driving end-to-end product lifecycle, including design, validation, and releases
• Oversee end-to-end ICSR case processing capabilities (intake through regulatory submission), ensuring efficiency, quality, and compliance
• Serve as product/IT lead for ArisGlobal LSMV, and manage ReporterX and XDI for intelligent data intake and integration (E2B, structured and unstructured sources)
• Enable seamless integration with RxLogix (RxL) to support signal detection, reporting, and analytics
• Drive adoption of automation and AI to reduce manual effort, improve data quality, and enhance throughput
• Ensure compliance with global PV regulations (FDA, EMA, ICH E2B, GVP) and maintain audit/inspection readiness
• Monitor system performance, SLAs, and data quality KPIs; lead issue resolution, risk mitigation, and continuous improvement initiatives
• Act as primary interface between IT and Pharmacovigilance business teams, aligning on priorities and delivery plans
• Partner with vendors (e.g., ArisGlobal, RxLogix) on product strategy, upgrades, and innovation
• Optimize cost, vendor performance, and system utilization
• Lead and develop a high-performing team, driving performance management, coaching, and a culture of accountability and continuous improvement

Required Qualifications

• Bachelor’s degree in Information Technology, Life Sciences, or related field
• 5-8+ years of experience in product management or IT application ownership in Pharmacovigilance

Hands‑on experience with

• ArisGlobal LifeSphere MultiVigilance (LSMV)
• ReporterX and XDI (data intake/integration frameworks)
• RxLogix (RxL) platform (signal detection/reporting/analytics)
• Strong understanding of ICSR case processing lifecycle and PV compliance requirements
• Experience working in GxP-regulated environments
• Exposure to Agile methodologies and modern technologies (AI/automation/data platforms)
• Excellent communication, leadership, and stakeholder management skills

Preferred Qualifications

• Experience leading global PV platform transformations or migrations
• Familiarity with regulatory inspections and audit support
• Knowledge of emerging technologies in AI-driven case processing and signal detection

• Work location 4123 Allschwil (BL)
• Workload 100%
• Employment start By agreement
• Employment duration Permanent
• Qualification skilled
• Work experience More than 3 years
• Education Bachelor’s degree from a university or equivalent
• English Orally : Basic knowledge Written : None
• By email [e-mail]