Head Of Regulatory and Quality Affairs

Business Be yourself, everyone else is already taken. For over 20 years, PERSUADERS RH has built its expertise in recruiting complex profiles and has developed a true legitimacy in supporting executives and COMEX members, coaching, transition management and HR consulting. We claim our difference by working beyond skills on the aptitude and personality of the profiles we support. We are intimately convinced that human qualities are the pillars of your success. The company, an award-winning startup with R&D in Toulouse and San Francisco, is a pioneer in the development of non-invasive breath analysis solutions for the screening, monitoring and detection of different biomarkers in exhaled breath. The company is developing its first product, a miniaturized breath analyzer for monitoring glucose concentration in pre-diabetics and type 2 diabetics. The device detects the type and concentration of volatile organic compounds in breath. The solution is pain-free, gentle, affordable, and produces significantly less waste than existing finger stick blood glucose or continuous glucose monitors. To support its growth, the company is seeking its future Head of Regulatory Affairs and Quality (M / F) . Later Main Responsibilities: Lead and oversee all regulatory and quality activities for the company’s products and services Ensure the company’s compliance with national and international regulations applicable to medical devices Develop and implement a robust quality management system compliant with ISO standards, other medical device ISO standards and good manufacturing practices Implement and supervise an effective risk management process Manage regulatory submission processes, obtaining authorizations, and product certification with relevant authorities Supervise internal and external audits related to quality and regulatory compliance Train and raise awareness among staff about regulatory requirements and quality practices Represent the company to regulatory bodies and professional associations LOCATION The position requires spending a significant amount of time in Toulouse, where the laboratory is located. Working from home is partially possible. TRAVEL The position entails regular travel within the country and overseas to meet with authorities, vendors, and other stakeholders. COMPENSATION For a qualified individual who meets these specifications, the Company is prepared to offer a competitive compensation package. This key position at the company requires solid expertise in medical device regulation and quality, as well as the ability to effectively manage regulatory processes and ensure company compliance. Profile Required Qualifications and Experience: Advanced degree in engineering, life sciences, or a related field Minimum of 5 years of experience in a regulatory and quality role for medical devices Excellent knowledge of regulations applicable to in vitro-diagnostics and medical devices (FDA, CE, etc.) Proficiency in ISO , ISO , IEC , HITRUST (including SOC2, NIST, ISO standards), and good manufacturing practices Proven experience in implementing and managing quality management systems In depth familiarity with the risk management process according to ISO Strong project management and problem-solving skills Hands on mentality Excellent written and verbal communication skills in French and English Other Valued Skills: Knowledge of the in vitro diagnostics field and analysis device technologies Experience in managing regulatory and quality teams Ability to work in a dynamic environment and meeting tight timelines Strong organizational skills and attention to detail Analytical and synthesis skills Entrepreneurship Experience in Diabetes a plus but not mandatory APPLY HERE #J-18808-Ljbffr