P2613 - CSV Lead — Debiopharm
- Location
- Lausanne
- Contract
- other
- Posted
- 78 days ago
Role overview
Together, we innovate, we impact, we grow !
At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases.
As a privately-owned Swiss biopharmaceutical company, we’re driven by science, but above all, by the people behind every treatment — the patients and their families.
- Together, we innovate, we impact, we grow !
- At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases.
- Strategy & Oversight: Evaluate, design, and implement the CSV strategy for both current and new systems, ensuring it is accurately reflected in procedural documents.
- Vendor & Project Integration: Contribute to vendor selection and qualification, providing pro-active quality oversight for GxP critical systems and processes.
Main responsibilities
- Strategy & Oversight: Evaluate, design, and implement the CSV strategy for both current and new systems, ensuring it is accurately reflected in procedural documents.
- Vendor & Project Integration: Contribute to vendor selection and qualification, providing pro-active quality oversight for GxP critical systems and processes.
- Execution & Validation: Direct the CSV approach for project teams, supervising the creation and approval of deliverables, test defects, and risk mitigation activities.
- Lifecycle Management: Oversee the computerized system portfolio, managing change controls, periodic reviews, and maintenance activities after "Business Go-live".
- Internal Advisory: Act as an expert advisor on CSV regulations, supporting AI projects from a regulatory/validation standpoint and mentoring staff on CSLC activities.
- Leadership & Quality: Manage, mentor and develop the CSV team, ensuring high-quality delivery across all portfolio initiatives, identify areas for process improvement, change management and assist with audit planning / CAPA formulation.
Additional details
- You will bridge the gap between innovation and compliance, ensuring that our digital evolution is supported by a pragmatic, risk-based validation framework that protects data integrity and patient safety across our portfolio.
Notes and original content
- Responsibilities
Questions about this listing
What salary does Debiopharm offer for this role?
Debiopharm lists CHF 79'500 - 120'500 gross per year for this position in Lausanne. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Debiopharm offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Debiopharm during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Vaud?
EU/EFTA residents living in the border zone of the country adjoining Canton Vaud can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Vaud's cantonal migration office or with HR during the application.
How do I apply for this position at Debiopharm?
Use the "Apply now" button on this page — it links directly to Debiopharm's original listing at apply.workable.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
