Associate Director

Requisition ID: 6311

Job Title: Associate Director, Regulatory Affairs - Remote

Job Country: United States (US)

Here at Avanos Medical, we passionately believe in three things:
•   Making a difference in our products, services and offers, never ceasing to fight for groundbreaking solutions in everything we do;
•   Making a difference in how we work and collaborate, constantly nurturing our nimble culture of innovation;
•   Having an impact on the healthcare challenges we all face, and the lives of people and communities around the world. At Avanos you will find an environment that strives to be independent and different, one that supports and inspires you to excel and to help change what medical devices can deliver, now and in the future.

Avanos is a medical device company focused on delivering clinically superior breakthrough solutions that will help patients get back to the things that matter. We are committed to creating the next generation of innovative healthcare solutions which will address our most important healthcare needs, such as reducing the use of opioids while helping patients move from surgery to recovery. Headquartered in Alpharetta, Georgia, we develop, manufacture and market recognized brands in more than 90 countries. Avanos Medical is traded on the New York Stock Exchange under the ticker symbol AVNS. For more information, visit .

Job Summary

The Associate Director, Regulatory Affairs, plays a critical leadership role in ensuring the organization's medical devices comply with global regulatory requirements, with a particular emphasis on the European Union Medical Device Regulation (EU MDR 2017/745). This position is responsible for developing and implementing regulatory strategies, managing regulatory submissions, and ensuring ongoing compliance to support product lifecycle management, market access, and business objectives. The Associate Director serves as a key liaison with regulatory agencies, notified bodies, and cross-functional teams, providing expertise and strategic guidance to navigate the evolving regulatory landscape.

As the Associate Director, Regulatory Affairs, you will lead the development and execution of regulatory strategies for the company's medical device portfolio, focusing on MDR compliance for CE marking and post-market surveillance. You will oversee regulatory submissions, technical documentation, and conformity assessment processes, ensuring alignment with regulatory requirements and business goals. This role involves collaboration with cross-functional teams, including Quality, R&D, Clinical, and Marketing, to drive timely product approvals and support regulatory aspects of product development and lifecycle management. Additionally, you will monitor regulatory changes, provide risk assessments, and implement strategies to maintain compliance and mitigate regulatory risks in global markets. The successful candidate will have deep expertise in MDR requirements and a strong ability to manage regulatory challenges while fostering a culture of compliance and continuous improvement.

Job Position Accountabilities / Expectations

Regulatory Strategy and Compliance
•   Develop and implement comprehensive regulatory strategies to support CE marking under the EU Medical Device Regulation (MDR 2017/745) for the company's medical device portfolio.
•   Ensure compliance with global regulatory requirements, including ISO 13485, FDA 21 CFR Part 820, and other applicable standards and regulations.
•   Lead the preparation, submission, and maintenance of regulatory documentation, including Technical Documentation and General Safety and Performance Requirements (GSPR)
•   Support/enable cross functional partners through participation and reviews of strategies associated with risk management, clinical evaluation, design verification and validation, post-market activities, etc. Regulatory Submissions and Approvals
•   Oversee regulatory submissions for CE marking and potentially other global markets, ensuring timely approval of new and existing products.
•   Coordinate with Notified Bodies and Competent Authorities, serving as the primary point of contact to address inquiries, audits, and inspections.
•   Review and approve regulatory aspects of marketing materials, labeling, and product claims to ensure compliance with applicable regulations. Cross-Functional Collaboration
•   Collaborate with R&D, Quality Assurance, Clinical Affairs, and Manufacturing teams to provide regulatory input during product development, design changes, and post-market activities.
•   Support clinical and preclinical activities by ensuring alignment with MDR clinical evidence requirements.
•   Participate in risk management activities, ensuring regulatory requirements are incorporated into the product lifecycle. Post-Market Compliance
•   Support and participate in regulatory audits performed by both internal and external authorities Regulatory Intelligence and Risk Management
•   Monitor, interpret, and communicate regulatory changes, trends, and guidance to ensure the organization remains proactive in compliance.
•   Provide regulatory risk assessments and mitigation strategies to support business objectives.
•   Implement best practices and continuous improvement initiatives to enhance regulatory processes and systems. Leadership and Training
•   Lead and mentor the regulatory affairs team, fostering a culture of collaboration, accountability, and excellence as aligned with the Avanos Values.
•   Provide regulatory training and guidance to internal stakeholders to ensure awareness and understanding of regulatory requirements.
•   Continue to increase knowledge in the areas of Regulatory Affairs, including, but not limited to, MDR 2017/745, ISO 13485, regulatory writing, regulatory strategy, regulatory risk and governing guidance and regulations.
The Associate Director will act as a key contributor to the global regulatory function, reporting as a trusted partner to the Senior Director of Global Regulatory Affairs.

Positions reporting to this job may include: Pr. Regulatory Affairs Specialist, Sr. Regulatory Affairs Specialist, and Regulatory Affairs Specialist

This position will work closely with the Sr. Director Regulatory Affairs in EU and team, as well as the EU Authorized Representative

External Interface :

International Regulatory Bodies (e.g., FDA, Health Canada, Notified Body, etc.), Distributors, and Suppliers,
•   Subject Matter Expertise: Demonstrate in-depth knowledge of MDR 2017/745, including clinical evaluation requirements, PMS, PMCF, risk management, and conformity assessments.
•   Timely Delivery: Ensure timely preparation and submission of regulatory documentation to meet project milestones and business timelines.
•   Effective Communication: Serve as a key regulatory liaison with internal and external stakeholders, communicating complex regulatory requirements in a clear and actionable manner.
•   Problem Solving: Proactively identify regulatory challenges and provide strategic solutions to minimize delays or risks to compliance.
•   Ethics and Compliance: Maintain the highest level of integrity and compliance, ensuring that all regulatory activities align with applicable laws, regulations, and company policies.
•   Adaptability: Remain agile in response to the evolving regulatory landscape, adjusting strategies and processes as needed to maintain compliance and achieve business objectives. This position is a leadership role requiring exceptional regulatory expertise, strong cross-functional collaboration, and a proactive approach to navigating the complexities of global medical device regulations, with a primary emphasis on MDR compliance.

Qualifications and Education:
•   Bachelor's degree in a relevant scientific, engineering, or medical discipline (e.g., Biology, Biomedical Engineering, Regulatory Science).
•   Advanced degree (e.g., Master's, Ph.D.) in a related field is preferred.
•   Regulatory Affairs Certification (RAC) or similar professional certification is a plus. Experience:
•   A minimum of 8 years of experience in regulatory affairs within the medical device industry, or 5 years with an advanced degree, and with at least 3-5 years in a leadership or management role .
•   Extensive experience with EU MDR 2017/745 , including technical documentation, clinical evaluation requirements, conformity assessments, and post-market surveillance processes.
•   Proven track record of successful regulatory submissions and approvals for CE marking and other global markets.
•   Experience working with Notified Bodies, Competent Authorities, and regulatory agencies.
•   Familiarity with global medical device regulations, including FDA 21 CFR Part 820, MDSAP, ISO 13485, and other applicable standards. Preferred Qualifications:
•   Knowledge of additional global regulatory frameworks (e.g., China NMPA, Japan PMDA, Canada, Australia) is highly desirable.
•   Experience with digital health technologies, software as a medical device (SaMD), or combination products is a plus.
•   This position requires a high level of regulatory expertise, leadership skills . click apply for full job details