Senior Director, Regulatory Affairs - Product Development

CryoLife, Inc.; Kennesaw (GA); Hybrid; USD 180,000 - 250,000; Full time

Benefits offered by this job

Equal Opportunity Employer

Job summary

Artivion, Inc. in the Atlanta area seeks an experienced Senior Director Regulatory Affairs, Product Development to set enterprise-level global regulatory strategy for its new-product portfolio and lead regulatory efforts from feasibility through approval, launch and lifecycle management.

You will manage senior regulatory staff, interact with FDA and global authorities, align regulatory plans with clinical evidence, labeling and marketing strategies, and collaborate across R&D, QA, Operations,

Qualifications

• Bachelor's degree in science, engineering, life sciences or related field required.
• Minimum 12 years of regulatory affairs experience with leadership in medical devices OR 10 years with engineering/advanced degree.
• Experience with Class II/III devices and global submissions (FDA/CE).

Responsibilities

• Set global regulatory strategies for emerging technology and product development.
• Lead portfolio-level regulatory planning for high-risk devices and approvals.
• Represent regulatory affairs to executive leadership and cross-functional teams.
• Oversee timely submissions to global regulatory agencies (FDA, EU MDR, etc.).

Skills

Regulatory strategy

Leadership

Regulatory submissions

Cross-functional

Executive communication

Education

Bachelor's degree in science or engineering

Job description

Locations

• Remote
• Regulatory Affairs
• Full-Time

• Kennesaw
  1655 Roberts Blvd NW
  Kennesaw, GA 30144, USA

Description

Company Overview:

Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons’ most difficult challenges in treating patients with aortic diseases. Artivion’s four major groups of products include: aortic stent grafts, surgical sealants, On-X mechanical heart valves, and implantable cardiac and vascular human tissues. Artivion has over 1,600 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, www.artivion.com .

Position Overview:

The Senior Director Regulatory Affairs, Product Development will be responsible for setting enterprise-level global regulatory strategy for Artivion's new product development portfolio and leading the regulatory approach for complex, high-risk medical device programs from early feasibility through approval, launch and lifecycle expansion.

This role will lead senior Regulatory Affairs management and staff, serve as a senior regulatory decision-maker for assigned programs and represent Artivion with global regulatory authorities, notified bodies and other external stakeholders. The position is accountable for anticipating regulatory risk, resolving complex submission and agency issues, and ensuring clear, timely and compliant regulatory execution across regions.

Responsibilities:

• Establish, approve and oversee global regulatory strategies for emerging technology, product development, product registrations, lifecycle management and market access with domestic and international regulatory agencies.
• Lead portfolio-level regulatory planning for complex high-risk devices, including regulatory pathway, claims, labeling, evidence, timelines, resource plans and approval risk.
• Serve as the senior Regulatory Affairs representative to executive leadership, program governance and cross-functional product development teams; advise on regulatory risk, tradeoffs and go/no-go decisions.
• Influence and manage emerging and acquired technology opportunities and support integrations, as needed.
• Oversee and ensure timely, high-quality submissions to global regulatory agencies, including US FDA pre-submissions, IDE, PMA, 510(k), PMA supplements, EU MDR technical documentation, CE Marking, deficiency responses and international strategies for registration.
• Lead, prepare for and negotiate regulatory authority interactions, including FDA meetings, notified body reviews, competent authority engagement, advisory panel preparation, formal correspondence and complex deficiency resolution.Advise on clinical evidence strategies to support global approvals, including IDE/pivotal study design alignment, endpoints, follow-up expectations, post-approval commitments, real-world evidence and benefit-risk framing.
• Interpret current and evolving global medical device regulations, standards and guidance; assess enterprise impact and drive implementation plans that support compliant innovation and market access. Support global compliance programs.
• Partner with R&D, Clinical, Quality, Operations, Supply Chain, Marketing, Commercial and Legal to integrate regulatory requirements into design controls, manufacturing changes, labeling, promotional claims, launch readiness and pre- & post-market commitments.
• Direct regulatory assessments for new technologies, design changes, labeling and claims, product discontinuations, development partnerships and business development opportunities, as applicable.
• Contribute to commercial plans and advise on strategies to achieve regionl and corporate objectives.
• Build, manage, mentor and succession-plan a high-performing Regulatory Affairs organization; set goals, allocate resources, manage budgets and establish metrics and processes that align with business objectives.
• Provide senior regulatory leadership for audits, inspections, escalations, field actions and compliance issues; maintain the highest standards of ethics, regulatory compliance and patient safety.

Qualifications:

• Bachelor's degree required in science, engineering, life sciences or related discipline; advanced degree in a relevant focus area preferred.
• Minimum 12 years of experience in regulatory affairs or the medical device industry with bachelor's degree, including significant leadership experience, OR
• Minimum 10 years of experience in regulatory affairs or the medical device industry with engineering degree and master's degree, including significant leadership experience.
• Extensive experience defining and executing global regulatory strategies for Class II/III and high-risk medical devices across new product development and lifecycle management.
• Proven success leading or substantially influencing successful submissions and approvals, including IDE, PMA, HDE, PMA supplements, EU MDR technical documentation/CE Marking and international registrations such as ANVISA, PMDA, and Health Canada.
• Knowledge of and expertise in global medical device regulations, particularly US FDA, EU MDR, Canada, Latin America and Asia Pacific requirements.
• Experience leading direct interactions and negotiations with FDA, notified bodies and global regulatory authorities, including pre-submissions, deficiency responses, advisory panel preparation and inspection support.
• Demonstrated ability to align regulatory strategy with clinical evidence generation, pivotal studies, benefit-risk assessments, labeling, claims and commercialization plans.
• Experience with global quality system regulations and standards, including US FDA QMSR/21 CFR Part 820, ISO 13485, ISO 14971, design controls and related medical device standards.
• Strong executive communication, influencing, negotiation and stakeholder management skills in complex, matrixed environments.
• Advanced analytical thinking skills; ability to understand principles of engineering, physiology, device design, medical device use and software/digital components, as applicable.
• Proven program and portfolio management skills with ability to assess, prioritize and complete multiple complex projects, tasks and responsibilities.
• Advanced personnel development, succession planning, budget/resource management and organizational design skills.
• High ethical standards, sound judgment and ability to lead through ambiguity while maintaining compliance, quality and patient safety focus.

Equal Opportunity Employer
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