Senior Director of Global Quality – Port St. Lucie, FL | Medical Components

 

Senior Director of Global Quality – Port St. Lucie, FL | Medical Components

Are you an experienced leader in quality management with a passion for improving medical products? We are looking for a Senior Director of Global Quality to oversee the quality systems, product excellence, and compliance for a leading medical components company in Port St. Lucie, FL. This is an exciting opportunity to drive global quality strategies, enhance operational performance, and ensure the highest standards in medical device manufacturing.

Lead the Quality Excellence of a Global Medical Components Company

Join a world-renowned medical components company in Port St. Lucie, FL, as the Senior Director of Global Quality. In this strategic leadership role, you will be responsible for shaping and executing quality strategies across global operations, ensuring product compliance with industry standards, and leading continuous improvement initiatives. The ideal candidate will have extensive experience in medical device quality management, a deep understanding of regulatory requirements, and the ability to foster a culture of quality across international teams. If you are passionate about improving healthcare through high-quality products, this is your chance to take the lead in shaping the future of medical component manufacturing.

Key Responsibilities of the Senior Director of Global Quality – Medical Components

Strategic Leadership & Quality Vision:
Develop and execute a global quality strategy that aligns with the company’s objectives, ensuring that all products meet the highest standards of quality and compliance. Lead the development of quality systems and processes that drive continuous improvement and innovation across the organization.

Operational Excellence & Compliance:
Oversee the company’s global quality management systems (QMS) and ensure that all manufacturing processes comply with regulatory standards and industry certifications. Ensure that production lines are optimized for efficiency, quality, and cost-effectiveness, while maintaining strict adherence to industry regulations and best practices.

Global Quality System Oversight:
Lead global teams in implementing and maintaining a comprehensive quality system across all locations. Ensure that quality assurance processes are standardized, effectively documented, and meet the expectations of both regulatory bodies and internal stakeholders.

Regulatory Compliance & Risk Mitigation:
Ensure that the company complies with all relevant regulations, including FDA, ISO, and other global standards. Proactively manage risk through audits, inspections, and compliance reviews to prevent quality issues and ensure timely resolution of non-compliance. Lead the development of corrective and preventive actions (CAPA) processes.

Team Leadership & Development:
Lead, mentor, and develop the global quality team. Foster a culture of quality excellence and continuous improvement, empowering teams to identify and solve quality challenges. Ensure that the team is equipped with the necessary tools, training, and support to meet the company’s high standards.

Stakeholder Communication & Reporting:
Establish clear communication channels with key internal and external stakeholders, including senior leadership, regulatory bodies, and suppliers. Provide regular updates on the status of quality initiatives, regulatory compliance, and performance metrics, using data-driven insights to inform decision-making and drive business results.

Customer & Supplier Quality Collaboration:
Collaborate with suppliers, customers, and internal departments to ensure that all products meet customer requirements and industry standards. Drive initiatives to improve supplier quality performance and strengthen partnerships with suppliers to ensure consistency in product quality.

Continuous Improvement & Innovation:
Drive a culture of continuous improvement by identifying areas for process optimization, reducing waste, and enhancing overall product quality. Lead quality improvement projects that support the company’s innovation goals, ensuring that new products meet quality expectations from concept through production.

Financial Management & Budgeting:
Manage the quality budget, ensuring that financial resources are effectively allocated to quality initiatives, tools, and systems that align with the company’s strategic goals. Optimize cost management without compromising quality or regulatory compliance.

Health, Safety, & Environmental Stewardship:
Ensure that the company’s quality practices are in line with health, safety, and environmental standards, promoting a safe working environment for all employees. Implement policies and procedures to minimize environmental impact while ensuring product quality and safety.

What the Client is Looking for in You

As the Senior Director of Global Quality – Medical Components, the client is seeking a highly skilled and experienced leader who can drive global quality management, foster a culture of excellence, and ensure compliance across all manufacturing processes. You should be a visionary in quality management with a proven ability to lead teams, optimize processes, and improve product quality in a regulated industry. The ideal candidate will be an exceptional communicator who can navigate the complexities of global operations while maintaining the highest standards of quality and compliance.

Proven Leadership in Global Quality Management

The client is looking for a seasoned leader with extensive experience in quality management within the medical device or medical components sector. You should have a successful track record of developing and implementing quality management systems that ensure product excellence and regulatory compliance. Experience in managing global teams, overseeing audits, and working with regulatory bodies like the FDA and ISO is essential. The ability to drive continuous improvement and lead complex quality initiatives on a global scale is highly valued.

Strategic Vision for Quality and Compliance

As the Senior Director of Global Quality, you must possess the strategic foresight to shape and execute a global quality strategy that aligns with the company’s objectives. The ideal candidate will be capable of identifying and addressing quality challenges, driving process optimization, and ensuring compliance across all operational functions. You should be able to anticipate regulatory trends and adapt quickly to the changing demands of the medical components industry.

Strong Regulatory and Risk Management Expertise

A deep understanding of regulatory requirements and risk management is key. The client seeks a leader who has experience working with regulatory bodies and understands the complexities of managing compliance across various markets. You should have a strong background in risk mitigation, auditing, and ensuring adherence to quality standards that meet or exceed industry regulations.

Proven Ability to Lead Cross-Functional Teams

The client values a leader who can inspire and manage a global quality team, driving collaboration across departments and regions. You should have experience leading cross-functional teams to implement quality initiatives, resolve issues, and continuously improve processes. Your leadership should foster a culture of accountability, innovation, and teamwork, ensuring that the global quality function is aligned with the company’s overall business objectives.

Customer-Focused Quality Leadership

The client is looking for a leader who places the customer at the center of quality management decisions. You should have a strong ability to translate consumer needs and product requirements into actionable quality strategies that ensure the delivery of high-quality medical components. Your focus on enhancing customer satisfaction through rigorous quality processes will be key to success in this role.

Strong Communication and Stakeholder Management

Effective communication with internal teams, external partners, and regulatory bodies is essential. The ideal candidate will be skilled in presenting quality performance data, driving discussions on product improvements, and ensuring transparency with stakeholders. Building strong relationships with key stakeholders will be essential to foster trust and support for quality initiatives.

Commitment to Operational Efficiency and Excellence

The client is looking for a leader who values operational excellence and is committed to improving processes and reducing waste while maintaining product quality. Your ability to manage the global supply chain, optimize manufacturing processes, and oversee quality control will be critical. The client values a leader who can ensure efficient, ethical, and compliant operations across all stages of production.

FAQs About the Role – Senior Director of Global Quality – Medical Components

1. What are the key responsibilities of the Senior Director of Global Quality in this role?
As the Senior Director of Global Quality, you will be responsible for leading the company’s global quality strategy, ensuring compliance with regulatory standards, and overseeing all quality management systems (QMS) across the organization. You will drive continuous improvement in quality processes, manage global teams, and ensure that products meet the highest industry standards. Additionally, you will be responsible for managing supplier quality, reducing risks, and maintaining strong relationships with key stakeholders, including regulatory bodies and external partners.

2. What qualifications and experience are required for this position?
The ideal candidate should have significant leadership experience in global quality management, preferably within the medical device or medical components sector. A strong background in regulatory compliance (e.g., FDA, ISO standards), quality assurance, and risk management is essential. The client is seeking a leader with experience in leading global teams, improving quality processes, and ensuring product excellence in a regulated environment. A relevant degree in engineering, quality management, or a related field is preferred, and certifications in quality management systems (e.g., Six Sigma, ISO certifications) are highly valued.

3. What leadership qualities are essential for this role?
The client is looking for a results-driven leader with a strong focus on operational excellence and a deep understanding of quality management in regulated industries. You should possess excellent decision-making skills, the ability to lead global teams, and a strong commitment to continuous improvement. Strong communication, relationship-building, and stakeholder management skills are essential, as is the ability to influence at all levels of the organization and ensure quality objectives are aligned with business goals.

4. What challenges can I expect in this role?
As the Senior Director of Global Quality, you will face challenges related to ensuring regulatory compliance across multiple regions, managing risks in the supply chain, and driving quality improvements in a complex, global production environment. The role requires effective management of diverse teams and resources to maintain high-quality standards while balancing cost efficiency. You will also need to address the evolving regulatory landscape and ensure the organization’s products continue to meet or exceed industry standards.

5. What is the expected impact of the Senior Director of Global Quality on the company’s success?
The Senior Director of Global Quality is expected to have a significant impact on the company’s success by ensuring the consistent delivery of high-quality medical components that meet customer expectations and regulatory requirements. Your leadership in quality management will drive continuous improvement, reduce operational risks, and enhance the company’s reputation for excellence. The role will directly contribute to maintaining regulatory compliance, ensuring product reliability, and fostering customer trust, which are crucial to the company’s growth and industry position.

6. What is the company’s culture and work environment like?
The company promotes a culture of excellence, innovation, and continuous improvement. They value leadership that fosters collaboration, accountability, and a strong focus on quality at every stage of the product lifecycle. You will be working in a dynamic and fast-paced environment where cross-functional collaboration is essential, and opportunities for personal and professional growth are abundant. The company is committed to providing a supportive work environment that encourages open communication and innovation, with a focus on delivering high-quality solutions in the medical components industry.

What Remuneration Can You Expect from This Job?

As the Senior Director of Global Quality – Medical Components based in Port St. Lucie, FL, you can expect a highly competitive and attractive compensation package, designed to reward top executive talent in the medical components industry. The remuneration for this role typically includes:

1. Base Salary
The base salary for a Senior Director of Global Quality in the medical components industry varies based on company size, market position, and the scope of responsibility. For a senior leadership role at a global scale, the annual base salary typically ranges from $180,000 to $300,000, with larger or more established companies offering higher salaries depending on experience and expertise.

2. Performance-Based Bonuses
In addition to a base salary, compensation packages often include annual performance-based bonuses, which are tied to key operational metrics such as quality improvements, regulatory compliance, cost savings, and efficiency gains. These bonuses can range from 20% to 50% of the base salary, depending on individual and company performance.

3. Equity & Stock Options
Many companies offer equity-based incentives such as stock options, restricted stock units (RSUs), or performance shares as part of the total compensation package. These incentives align the Senior Director’s interests with long-term business goals and shareholder value. Equity grants can form a significant portion of the overall compensation, particularly in companies with high growth potential.

4. Long-Term Incentive Plans (LTIPs) & Profit-Sharing
Some companies provide long-term incentive plans (LTIPs) or profit-sharing programs that reward the Senior Director for sustainable success over multiple years. These programs are designed to align the leadership’s interests with the company’s long-term performance and profitability.

5. Executive Benefits & Perks
As a Senior Director, you will be entitled to a comprehensive executive benefits package, which may include:

• Health, dental, and vision insurance
• 401(k) plans with company contributions
• Executive retirement plans
• Company-provided vehicles or travel allowances
• Wellness and fitness programs
• Expense accounts for business development and travel

6. Signing Bonuses & Relocation Assistance
For top candidates, the company may offer signing bonuses or relocation assistance. These one-time incentives may range from $25,000 to $100,000 depending on the candidate’s experience and the complexity of relocation requirements.

Total Compensation Potential

When factoring in base salary, bonuses, equity options, and additional benefits, the total compensation for the Senior Director of Global Quality can range from $250,000 to $500,000 annually, with potential for significant growth in larger or rapidly expanding organizations.

How to Apply

If you are a dynamic and strategic leader with extensive experience in the Consumer Packaged Goods (CPG) industry, we encourage you to apply for the Senior Director of Global Quality – Medical Components role in Port St. Lucie, FL. This is an exceptional opportunity to lead the global quality strategy, drive operational excellence, and implement quality systems to ensure compliance and product integrity across the medical components division.

To apply, please submit the following:

1. Resume: Highlight your leadership experience, technical expertise in quality management, and your track record in driving quality improvements and regulatory compliance within the medical components or similar industries.
2. Cover Letter: Detail your experience in global quality leadership, including your expertise in managing cross-functional teams, implementing quality systems, optimizing supply chain processes, and achieving continuous improvement. Be sure to emphasize your ability to navigate the complexities of the medical industry and your success in delivering measurable results.

This is a high-impact career opportunity where you will play a key role in shaping the company’s quality strategy, ensuring product excellence, and driving continuous improvement in a global market.

Apply today to take the next step in your executive career as the Senior Director of Global Quality!

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

Tags:
Senior Director | Medical Components Quality | Global Quality Leadership | Regulatory Compliance | Quality Systems | Supply Chain Optimization | Medical Device Leadership | Continuous Improvement | Executive Jobs