ki:elements pioneers speech-based biomarkers as tools for clinical research. We are looking for a Quality & Regulatory Lead to bridge the gap between our agile company and the rigorous demands of global clinical trials .

Regulatory excellence is central to our operations. Reporting directly to the CEO, you will own our compliance roadmap, shape our regulatory strategy, refine our QMS, and ensure our technology meets the highest standards for both FDA/EMA and our global pharma partners.

Tasks

• Lead the roadmap development and management for key certifications, specifically FDA 510(k) clearance and EU MDR.

• Ensure our technology aligns with clinical trial requirements , including 21 CFR Part 11 and GCP/GxP standards.

• Oversee our QMS (ISO 13485 / ISO 27001).

• Manage and mentor the existing RA/QA staff. You will set priorities, review technical documentation, and foster a culture of "Compliance by Design."

• Act as the primary point of contact for external audits and stringent technical assessments from pharmaceutical partners.

Requirements

• 5–10 years in RA/QA, specifically focused on Software as a Medical Device (SaMD).

• Deep familiarity with FDA 510(k), EU MDR, ISO 13485, ISO 14971, and 21 CFR Part 11. Experience with ISO 27001, IEC 62304 and GDPR is a significant plus.

Benefits

• ki:elements offers a four-day workweek (100% = 32 hours; Mo-Th)

• Remote or at our offices in Berlin & Saarbrücken.

• Be part of a pioneering company at the forefront of healthcare innovation.

• Work with a talented and passionate team dedicated to making a difference.

• 73.000€ - 92.000€ in full time (100%); part-time equivalent.

If our profiles match, we would be delighted to hear from you.