Associate Director (Regulatory Affairs)
My client are a dynamic and innovative medical technology company focused on developing advanced healthcare solutions. As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory Affairs.
Title: Associate Director (Regulatory Affairs)
Location: 2-3 Day on-site
Type: Full-time
Key Responsibilities
* Lead and oversee regulatory affairs activities related to Medical Device Regulation (MDR) compliance.
* Guide the company through the MDR transition process for Medical Device Class IIa or above products.
* Manage a team of regulatory affairs professionals, providing mentorship and leadership.
* Ensure timely submissions and approvals for regulatory filings and compliance documentation.
* Collaborate cross-functionally with R&D, Quality Assurance, and Clinical teams to support product development and regulatory strategies.
* Stay updated on regulatory changes and requirements to ensure company compliance.
Qualifications and Experience
* Bachelor's degree in a related scientific or technical field; advanced degree preferred.
* Minimum 8 years of experience in regulatory affairs within the medical technology industry.
* Proven success in leading Medical Device Class IIa or above products through the MDR process.
* Strong knowledge of European regulatory requirements and standards (MDR, ISO 13485, etc.).
* Experience managing a regulatory affairs team is desirable.
* Excellent communication and interpersonal skills, with the ability to interact effectively with internal and external stakeholders.
* Strategic thinker with the ability to influence decision-making at the executive level.
Benefits
* Competitive salary and benefits package.
* Opportunity to work in a collaborative and innovative environment.
* Direct involvement in shaping the regulatory strategy of a growing medical technology company.
* Reporting directly to the co-owners of the business, providing significant status and influence within the organization.
If you are a proactive and driven regulatory affairs professional looking for an exciting opportunity to lead MDR compliance efforts and contribute to the growth of a cutting-edge medical technology company, we encourage you to apply.