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Regulatory Affairs Specialist at Roche - ApplyBlast

Regulatory Affairs Specialist

Roche

1 day ago

4.1 on Glassdoor

Sant Cugat del Vallès, Catalonia, Spain

Onsite

Full Time

Junior

0 applicants

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About this role

The Regulatory Affairs Specialist at Roche partners with cross-functional teams and external stakeholders to bring life-changing diagnostic solutions to market. The role involves preparing high-impact submission dossiers for Health Authority approvals and championing agile principles within the Oncology In-vitro Diagnostics (IVD) team. This position focuses on regulatory strategy, compliance, and driving efficiency through innovation and digital tools.

Responsibilities

Lead preparation of registration dossiers for Health Authority approvals
Formulate regulatory submission plans to secure global market access
Champion agile principles to drive regulatory milestones in IVD team

Skills

About Roche

roche.com

Headquarters

Basel, Basel-Stadt, Switzerland

Company Size

10001+ employees

Founded

1896

View Profile

As a pioneer in healthcare, we have been committed to improving lives since the company was founded in 1896 in Basel, Switzerland. Today, Roche creates innovative medicines and diagnostic tests that help millions of patients globally.