Manager Technical Product Management (m/w)
- Unternehmen
- Actelion Pharmaceuticals Ltd
- Ort
- Allschwil
- Datum
- 08.08.2026
- Referenznummer
- 332423
Opportunity Overview
An exciting opportunity awaits an experienced professional who is ready to enhance the Pharmacovigilance (PV) technology landscape, focusing on case processing systems and operational excellence. In this pivotal role, collaboration with Safety, Regulatory, and IT teams is essential to drive innovation, scalability, and compliance across global PV platforms.
Key Responsibilities
- Own and execute the product roadmap for PV case processing and safety platforms, aligning technology solutions with business needs.
- Lead Agile delivery by managing backlog priorities and overseeing the full product lifecycle, including design, validation, and releases.
- Ensure efficient, compliant ICSR case processing capabilities, from intake to regulatory submission.
- Act as the product/IT lead for ArisGlobal LSMV, managing ReporterX and XDI for intelligent data intake and integration.
- Facilitate seamless integration with RxLogix (RxL) to enhance signal detection, reporting, and analytics.
- Drive the adoption of automation and AI to minimize manual input, improve data quality, and enhance throughput.
- Maintain compliance with global PV regulations and uphold audit/inspection readiness.
- Monitor system performance, SLAs, and data quality KPIs, leading efforts for issue resolution and continuous improvement.
- Serve as the primary liaison between IT and Pharmacovigilance teams, ensuring aligned priorities and effective delivery plans.
- Collaborate with vendors on product strategy, upgrades, and innovative solutions.
- Optimize costs, vendor performance, and system utilization.
- Lead and nurture a high-performing team, fostering a culture of accountability and continuous improvement.
Required Qualifications
- Bachelor’s degree in Information Technology, Life Sciences, or a related field.
- 5–8+ years of experience in product management or IT application ownership within Pharmacovigilance.
- Hands-on expertise with ArisGlobal LifeSphere MultiVigilance (LSMV), ReporterX, XDI, and RxLogix (RxL).
- Comprehensive understanding of the ICSR case processing lifecycle and PV compliance requirements.
- Experience in GxP-regulated environments.
- Familiarity with Agile methodologies and modern technologies such as AI and automation.
- Exceptional communication, leadership, and stakeholder management skills.
Preferred Qualifications
- Experience leading global PV platform transformations or migrations.
- Familiarity with regulatory inspections and audit support processes.
- Knowledge of emerging technologies in AI-driven case processing and signal detection.