Regulatory Affairs Manager — Roche
- Location
- Sant Cugat del Vallès
- Contract
- full-time
- Posted
- 21 days ago
Role overview
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
- At Roche you can show up as yourself, embraced for the unique qualities you bring.
- Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
- Key Responsibilities
- As an International Regulatory Affairs Professional at Roche, you will be responsible for:
Main responsibilities
- Key Responsibilities
- As an International Regulatory Affairs Professional at Roche, you will be responsible for:
- Leading and supporting regulatory strategies for global IVD/MD instruments and software submissions
- Ensuring compliance with international regulatory requirements and standards
- Collaborating with cross-functional teams, including R&D, Quality, and Clinical, to drive regulatory initiatives
- Providing regulatory guidance to support product development and lifecycle management
- Staying abreast of evolving regulatory trends and up‐ dates, and implementing best practices Requirements
- Bachelor’s Degree in Life Sciences, Regulatory Affairs, or a related field
- 5 to 7 years of experience in Regulatory Affairs ( Regulatory, R&D, Quality and/or Clinical), with some experience in healthcare regulatory affairs
- In-depth knowledge of global regulatory requirements, guidelines, and procedures especially for IVD instruments & software
Company and context
- Strong organizational and communication skills
- Ability to multitask and effectively manage multiple projects simultaneously
- Self-motivated and capable of working independently in a self-management environment
- Experience in IVD instrument and/or software development Why Roche
- Collaborative and innovative work environment
- Opportunity to make a meaningful impact on patients' lives globally
- Competitive compensation and benefits package
- Professional development and growth opportunities within a leading global healthcare organization
- If you are a dedicated professional who thrives in a fast-paced environment and is passionate about contributing to the
- International Regulatory Affairs landscape, we want to hear from you!
Additional details
- Join Roche, where every voice matters.
- At Roche, we believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future.
- passionate about transforming patients’ lives and we are brave in both decision and action. And we believe that good business
- Staying abreast of evolving regulatory trends and up‐ dates, and implementing best practices
- Experience in IVD instrument and/or software development
- relevant experience and qualifications. A healthier future drives us to innovate.
Notes and original content
- The Position
- passionate about transforming patients’ lives and we are brave in both decision and action.
- And we believe that good business
- Requirements
- relevant experience and qualifications.
- Who we are
- A healthier future drives us to innovate.
Questions about this listing
What salary does Roche offer for this role?
Roche lists CHF 85'500 - 129'500 gross per year for this position in Sant Cugat del Vallès. 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 Roche 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 Roche 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 Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel 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 Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Roche?
Use the "Apply now" button on this page — it links directly to Roche's original listing at roche.wd3.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
