P2624 - Global Regulatory Affairs Specialist/Manager — Debiopharm
- Location
- Lausanne
- Contract
- other
- Posted
- 18 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.
- Key Responsibilities:
- Strategy & Submissions: Support senior team members in developing and executing global regulatory strategies.
- Being part of a company where innovation, collaboration, and impact aren’t just values — they’re how we work every day
- Partner with teams across disciplines, at the forefront of oncology and anti-infective development
Main responsibilities
- Key Responsibilities:
- Strategy & Submissions: Support senior team members in developing and executing global regulatory strategies.
What the company offers
- Being part of a company where innovation, collaboration, and impact aren’t just values — they’re how we work every day
- Partner with teams across disciplines, at the forefront of oncology and anti-infective development
- An inclusive and respectful workplace — proud to be Equal-Pay certified
- Grow in a culture that values people, purpose, and performance A chance to grow, share, and shape the future of healthcare
Application process
- Assist in managing external vendors (e.g., CROs) and preparing/tracking multi-jurisdictional filings (INDs/CTAs, Briefing Documents, Orphan Drug Applications, PIP/PSP, Fast Track, Breakthrough Designation, PRIME, etc.).
- Cross-Functional Collaboration: Act as the Regulatory Affairs representative on cross-functional sub-teams, including Clinical Study Teams.
- Partner with functional experts to coordinate seamless input into regulatory documentation.
- Document Review: Actively participate in the review of key regulatory-relevant documents, such as Clinical Study Protocols, Clinical Study Reports, DSURs, and related filings.
- Landscape Assessment: Maintain up-to-date knowledge of the global competitive and regulatory landscape, evaluating the potential impact of changes on assigned projects.
- Process Excellence: Contribute to establishing and revising Standard Operating Procedures (SOPs) to enhance process efficiency and ensure ongoing regulatory compliance.
Additional details
- Permanent role, Full-time | Location: Lausanne, Switzerland
- Grow in a culture that values people, purpose, and performance A chance to grow, share, and shape the future of healthcare
Notes and original content
- Your Mission:
- Grow in a culture that values people, purpose, and performance
- A chance to grow, share, and shape the future of healthcare
Questions about this listing
What salary does Debiopharm offer for this role?
Debiopharm lists CHF 116'500 - 162'500 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.
