VP of Post-Market Surveillance – Tampa, FL | Implantable Devices

 

VP of Post-Market Surveillance – Tampa, FL – Implantable Devices

Are you a regulatory and quality leader passionate about improving patient outcomes and ensuring product safety in the medical device industry? We are seeking a Vice President of Post-Market Surveillance to join a leading implantable medical device company based in Tampa, FL. This high-impact role offers the opportunity to lead surveillance strategy, manage risk, and drive continuous product improvement across a global portfolio. If you thrive at the intersection of innovation, compliance, and patient safety, this executive leadership role is for you.

Lead Global Post-Market Excellence in Tampa, FL

A cutting-edge implantable medical device manufacturer in Tampa, FL is looking for a Vice President of Post-Market Surveillance to spearhead its global compliance and quality initiatives. The ideal candidate will bring deep expertise in post-market surveillance, regulatory affairs, and risk management, with a strong background in Class III medical devices. This is a unique opportunity to lead cross-functional teams, collaborate with regulatory bodies, and shape the company’s commitment to quality and patient safety on a global scale.

Key Responsibilities of the Vice President of Post-Market Surveillance – Implantable Devices

Post-Market Strategy & Execution: Develop and lead a comprehensive post-market surveillance (PMS) strategy in compliance with FDA, EU MDR, and global regulatory requirements. Align PMS processes with product lifecycle management and corporate objectives to ensure long-term device safety and effectiveness.

Adverse Event & Complaint Management: Oversee the intake, investigation, documentation, and resolution of complaints and adverse events. Ensure timely and accurate reporting to regulatory authorities and continuous feedback into risk management and product improvement processes.

Risk Management & Mitigation: Lead cross-functional teams in conducting trend analysis, risk assessments, and root cause investigations. Implement corrective and preventive actions (CAPAs) to mitigate safety risks and improve patient outcomes.

Regulatory Reporting & Compliance: Ensure all post-market activities comply with international regulations and standards, including MDR, ISO 13485, and FDA 21 CFR Part 803. Manage submission of medical device reports (MDRs), vigilance reports, and periodic safety update reports (PSURs) as required.

Surveillance Analytics & Data Utilization: Leverage data analytics to identify emerging safety signals, trends, and quality issues. Develop dashboards, KPIs, and metrics to provide visibility into product performance and guide executive decision-making.

Collaboration with R&D and Quality: Partner with R&D, Quality, and Regulatory teams to feed post-market insights into new product development, design improvements, and clinical strategies. Drive a culture of continuous improvement grounded in real-world data.

Regulatory Authority Engagement: Serve as the primary liaison for post-market matters with the FDA, Notified Bodies, and other global regulatory authorities. Lead audit readiness efforts and respond to regulatory inspections and inquiries.

Team Leadership & Development: Build and lead a high-performing global post-market surveillance team. Foster a collaborative, compliant, and proactive culture focused on quality, transparency, and patient safety.

Customer Communication & Support Integration: Align customer service and technical support teams with PMS activities to ensure consistent messaging, timely communication, and closure of field issues or recalls when necessary.

Documentation & Systems Oversight: Ensure accurate documentation, record-keeping, and maintenance of post-market systems, including electronic complaint handling and PMS databases. Lead system upgrades and digital transformation initiatives where applicable.

What the Client is Looking for in You

As the Vice President of Post-Market Surveillance – Implantable Devices, the client is seeking an accomplished quality and regulatory leader with deep expertise in post-market processes within the medical device industry. You should be a detail-oriented, compliance-driven executive with a passion for patient safety, a track record of managing complex regulatory landscapes, and the ability to lead global teams in a highly regulated environment.

Extensive Experience in Post-Market Surveillance & Regulatory Affairs

The client is looking for a senior leader with a proven track record in managing global post-market surveillance programs, particularly within Class II/III implantable devices. You should have deep knowledge of FDA regulations, EU MDR, ISO standards, and international reporting requirements. Experience handling adverse events, field actions, and post-market data analysis is essential.

Strategic Thinker with Risk-Based Approach

You must demonstrate a strategic mindset with the ability to design and implement risk-based post-market strategies that align with evolving regulatory expectations. The ideal candidate understands how to transform surveillance data into actionable insights, enabling safer and more effective product performance in real-world conditions.

Leadership in Cross-Functional and Global Environments

The client values candidates who have led high-performing, cross-functional teams across geographies. You should be capable of influencing stakeholders across Quality, R&D, Clinical, Regulatory, and Operations to ensure continuous improvement and seamless execution of surveillance initiatives.

Strong Analytical and Decision-Making Skills

A deep understanding of complaint data analysis, trend identification, and root cause investigation is key. The ideal candidate can make informed, data-driven decisions that enhance product safety and compliance while managing business impact and regulatory risk.

Effective Communicator with Regulatory Authorities

You should bring proven experience interfacing with the FDA, Notified Bodies, and other regulatory agencies. The ability to lead audit responses, manage inspections, and maintain clear, confident communication with external authorities is a must.

Commitment to Compliance, Quality, and Patient Safety

Above all, the client seeks a leader who is uncompromising in their commitment to quality and ethical practices. You must possess the drive to ensure compliance across all global post-market activities while championing a culture of patient safety and regulatory integrity.

Track Record of Digital System Implementation and Improvement

Experience implementing and optimizing complaint handling and PMS systems, including electronic solutions and data management tools, is highly desirable. Familiarity with software validation, audit trails, and GxP compliance will set you apart.

FAQs About the Role – Vice President of Post-Market Surveillance – Implantable Devices

1. What are the key responsibilities of the Vice President of Post-Market Surveillance in this role?

   As the Vice President of Post-Market Surveillance, you will be responsible for overseeing the company’s post-market surveillance strategy, ensuring the safety and effectiveness of implantable devices post-launch. This includes managing adverse event reporting, regulatory compliance, and risk mitigation efforts. You will lead cross-functional teams, work closely with R&D and Quality, and engage with regulatory authorities to ensure compliance with industry standards such as FDA regulations and EU MDR. You will also drive product improvements based on post-market data and trends, ensuring continuous product safety and quality.

2. What qualifications and experience are required for this position?

   The ideal candidate will have extensive experience in post-market surveillance or regulatory affairs within the medical device industry, specifically with implantable devices. You should possess a deep understanding of FDA and global regulatory requirements, including adverse event reporting and vigilance systems. A background in quality management, risk management, and data analytics is essential. A degree in a relevant field such as biomedical engineering, life sciences, or regulatory affairs is preferred. Previous leadership experience in post-market roles is highly valued.

3. What leadership qualities are essential for this role?

   The client is seeking a strong leader who is proactive, detail-oriented, and highly analytical. You must be able to lead cross-functional teams effectively, fostering collaboration across R&D, regulatory, quality, and manufacturing teams. Strong communication skills are key, as you will be responsible for reporting to regulatory bodies, engaging with senior leadership, and managing stakeholder expectations. You should also have a deep commitment to patient safety and regulatory compliance while promoting continuous improvement in post-market processes.

4. What challenges can I expect in this role?

   As the Vice President of Post-Market Surveillance, you will face challenges such as keeping up with evolving regulatory requirements, managing complex global compliance issues, and responding to emerging safety signals in the post-market environment. Additionally, you will need to balance the demand for operational efficiency with maintaining a patient-first mindset, all while mitigating risks associated with adverse events and product performance issues.

5. What is the expected impact of the Vice President of Post-Market Surveillance on the company’s success?

   The Vice President of Post-Market Surveillance will play a crucial role in maintaining product safety and ensuring compliance with global regulatory standards, which directly impacts the company’s reputation, legal standing, and overall market success. By driving data-driven insights and continuous product improvements, you will help minimize risk and enhance patient outcomes, all of which contribute to the company’s long-term growth and sustainability.

6. What is the company’s culture and work environment like?

   The company fosters a culture of collaboration, transparency, and patient safety. You will work in a dynamic environment that prioritizes compliance, innovation, and continuous learning. The company values individuals who take a proactive approach to problem-solving and who are passionate about making a positive impact on patient health. There is an emphasis on teamwork, accountability, and empowering leaders to drive positive change across the organization.

What Remuneration Can You Expect from This Job?

As the Vice President of Post-Market Surveillance for Implantable Devices in Tampa, FL, you can expect a competitive compensation package that reflects the seniority of the role and the critical nature of the responsibilities. The remuneration for this role typically includes:

1. Base Salary

   The base salary for the Vice President of Post-Market Surveillance will vary depending on factors such as the company’s size, market position, and the candidate’s experience. In a mid-to-large-sized medical device company, the annual base salary can range from $200,000 to $350,000, with larger organizations or those in high-growth markets offering even higher salaries.

2. Performance-Based Bonuses

   In addition to the base salary, a performance-based bonus is typically offered, aligned with key organizational metrics such as product safety, regulatory compliance, and market performance. The bonus structure can range from 20% to 50% of the base salary, contingent upon individual performance and company objectives.

3. Equity & Stock Options

   Many companies in the medical device industry offer equity incentives, such as stock options or performance shares, to align executive compensation with the long-term success of the company. Depending on the company’s valuation, these equity grants can constitute a significant portion of the total compensation package and offer long-term financial rewards.

4. Profit-Sharing & Long-Term Incentive Plans (LTIPs)

   Some companies offer profit-sharing schemes or LTIPs to reward sustained performance. These plans are designed to incentivize executives to focus on long-term organizational growth and profitability. LTIPs can be a significant source of income over several years.

5. Executive Benefits & Perks

   As part of the total compensation package, the Vice President of Post-Market Surveillance is likely to receive comprehensive executive benefits, including:

   • Health, dental, and vision insurance

   • 401(k) or pension plans with company contributions

   • Executive retirement plans

   • Company-provided vehicles or travel allowances

   • Executive wellness programs

   • Expense accounts for business-related travel and events

6. Signing Bonuses & Relocation Assistance

   For highly qualified candidates, companies may offer signing bonuses or relocation assistance to make the transition easier. These one-time incentives typically range from $25,000 to $100,000, depending on the company and the candidate’s qualifications.

Total Compensation Potential

When factoring in the base salary, performance bonuses, stock options, and other incentives, total compensation for a Vice President of Post-Market Surveillance in the medical device sector can range from $300,000 to $600,000 annually, with potential for higher earnings in high-growth or publicly traded companies. The total package may also include long-term financial benefits through equity and profit-sharing incentives.

How to Apply

If you are a strategic and experienced leader with a proven track record in post-market surveillance, regulatory compliance, and product safety in the medical device industry, we invite you to apply for the VP of Post-Market Surveillance – Implantable Devices role in Tampa, FL. This is an exciting opportunity to lead a high-performing team, ensure the safety and effectiveness of implantable devices, and drive the company’s growth through strong regulatory oversight and risk management.

To apply, please submit your resume and a cover letter that highlights your experience in post-market surveillance, regulatory compliance, and risk management. In your cover letter, we encourage you to provide examples of your leadership in ensuring product safety, collaborating with cross-functional teams, and your ability to navigate regulatory challenges in the medical device industry.

This is a high-impact leadership role where you will have the opportunity to influence the safety and success of implantable devices globally. Apply today to take the next step in your executive career as the Vice President of Post-Market Surveillance in Tampa, FL!

For more information or to explore similar opportunities, visit our Medical Device Executive Recruiters Page.

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Vice President | Post-Market Surveillance | Implantable Devices | Medical Device Industry Leadership | Regulatory Compliance | Product Safety | Risk Management | Post-Market Risk Analysis | Executive Medical Device Jobs