Senior Regulatory Affairs Specialist

As a Senior Regulatory Affairs Specialist, you will be Flinn's in-house regulatory domain expert, delivering high-quality regulatory intelligence services to MedTech customers across various regulatory challenges.

Requirements

• Broad regulatory expertise: Solid, hands-on experience interpreting and applying regulatory requirements across MedTech — focusing on MDSAP & EU regulations and standards.
• Customer orientation: You communicate technical regulatory content clearly and confidently to diverse audiences, from QA managers to C-level stakeholders.
• Digital affinity: You genuinely enjoy working with digital tools, and you actively seek out smarter, more efficient ways to do your work.
• Entrepreneurial self-organisation: You manage your own workload, deadlines, and customer commitments with a high degree of independence.
• Intellectual curiosity and adaptability: Regulatory landscapes evolve constantly. You stay ahead by reading widely, asking questions, and updating your understanding — remaining rigorous without becoming rigid.
• Attention to detail and diligence: Regulatory work leaves no room for sloppy interpretation. You are thorough, precise, and take quality seriously in every deliverable.
• Communication skills: Excellent written and spoken English is required; German is a strong plus given our core European customer base.

Benefits

• Flexible working hours, remote flexibility, and regular team time in Vienna
• Employee-friendly equity package, including fair vesting terms and profit-sharing opportunities
• Regular onboarding, advisory workshops, and periodic regulatory reviews
• Autonomy and clear ownership in a high-trust, low-ego environment
• Professional, high-standard environment that supports long-term personal and career development