Roche is seeking a Regulatory Program Specialist for a one-year fixed-term position, emphasizing a culture of personal expression, collaboration, and innovation. The role involves managing regulatory information, coordinating submissions, and supporting process improvements within a global context, targeting candidates with 1-2 years of relevant experience
Job Summary
The role involves managing regulatory information and executing submission processes to maintain the company's License to Operate through GxP compliance.
Candidates will collaborate across multiple departments including PT, PD, pRED, and gRED to align data monitoring and system workflows globally.
Roche offers a culture that encourages personal expression, open dialogue, and genuine connections where every voice matters in building a healthier future.
Matching Summary
Match Score: 80
Roche is seeking a Regulatory Program Specialist for a one-year fixed-term position, emphasizing a culture of personal expression, collaboration, and innovation. The role involves managing regulatory information, coordinating submissions, and supporting process improvements within a global context, targeting candidates with 1-2 years of relevant experience.
Skills & Requirements
Must-have
Manage regulatory data submissions
Coordinate document management eCTD
Ensure GxP compliance adherence
Partner with key stakeholders globally
Nice-to-have
Creative problem solving abilities
Mentor junior colleagues effectively
Proactively seek learning opportunities
Influence project outcomes internally
Key Requirements
1-2+ years of related experience
BA or BS degree in biology, chemistry, pharmacy, or English