VP of Quality Engineering – St. Petersburg, FL | Sterile Packaging

Are you an experienced leader in quality engineering with a focus on sterile packaging? We are seeking a VP of Quality Engineering to oversee the quality assurance and control of sterile packaging processes in St. Petersburg, FL. This senior leadership role offers a unique opportunity to shape and implement best practices, drive continuous improvement, and ensure the highest standards of quality in the packaging industry. If you have a passion for operational excellence and a commitment to delivering safe, high-quality products, this is your opportunity to lead an innovative and essential aspect of the business.

Shape the Future of Sterile Packaging Quality

In St. Petersburg, FL, a leading company in sterile packaging is looking for a Vice President of Quality Engineering to spearhead its quality assurance initiatives. The successful candidate will bring deep expertise in quality engineering, regulatory compliance, and the sterile packaging process. This role requires a strategic thinker with a hands-on approach to managing quality systems, optimizing manufacturing processes, and ensuring product integrity in highly regulated environments. If you are ready to take on a transformative role in a growing sector, we invite you to make a difference in the quality engineering domain.

Key Responsibilities of the VP of Quality Engineering – Sterile Packaging

Strategic Quality Leadership: Develop and implement a comprehensive quality strategy for sterile packaging that aligns with the company’s long-term goals. Drive continuous improvement initiatives, ensuring the highest standards of quality are maintained throughout the product lifecycle, from design to distribution.

Quality Systems & Compliance: Oversee the development, implementation, and monitoring of quality management systems (QMS) that adhere to industry standards and regulatory requirements. Ensure compliance with FDA, ISO, and other relevant regulations for sterile packaging and maintain rigorous documentation practices.

Operational Excellence in Packaging: Lead efforts to optimize manufacturing processes in sterile packaging, focusing on efficiency, scalability, and cost-effectiveness. Collaborate with engineering and production teams to identify opportunities for process improvements, reduce waste, and enhance product quality.

Risk Management & Issue Resolution: Identify and mitigate risks associated with sterile packaging processes. Implement proactive strategies for root cause analysis and corrective actions to address quality issues and prevent recurrence, ensuring minimal impact on production and customer satisfaction.

Team Leadership & Development: Lead and mentor a team of quality engineers and professionals, fostering a culture of accountability, collaboration, and continuous learning. Provide guidance and professional development opportunities to ensure the team’s growth and alignment with organizational goals.

Supplier & Vendor Quality Management: Manage supplier relationships, ensuring that external partners meet quality standards for sterile packaging. Conduct supplier audits and assessments, negotiate quality agreements, and ensure consistent quality in materials and components used in packaging.

Data-Driven Quality Insights: Utilize data analytics and performance metrics to monitor and assess the effectiveness of quality processes. Develop reports and dashboards that provide key insights into quality performance, trends, and opportunities for improvement.

Customer & Stakeholder Engagement: Build strong relationships with internal stakeholders, including production, R&D, and regulatory teams, to ensure alignment on quality objectives. Address customer concerns related to product quality and work with external customers to ensure satisfaction and regulatory compliance.

Regulatory Compliance & Audits: Lead internal and external audits to ensure compliance with industry regulations and corporate standards. Stay up to date with changes in regulatory requirements and ensure the organization is well-prepared for inspections and audits.

Innovation in Quality Control: Drive innovation in quality control processes and technologies, integrating new tools, techniques, and practices to stay ahead of industry advancements. Evaluate and implement advanced technologies that enhance quality assurance and streamline sterile packaging operations.

What the Client is Looking for in You

As the VP of Quality Engineering – Sterile Packaging, the client is seeking a highly skilled and experienced leader in quality engineering who can drive excellence in sterile packaging processes. You should be a results-oriented individual who thrives in a dynamic environment and has a proven ability to implement quality assurance programs while ensuring strict compliance with industry regulations.

Proven Leadership in Quality Engineering

The client is looking for a seasoned leader with significant experience in quality engineering, particularly in sterile packaging. You should have a strong track record of leading quality assurance teams, implementing robust quality management systems, and driving continuous improvement initiatives in highly regulated environments. Your experience in managing complex packaging processes and mitigating risks will be highly valued.

Expert in Sterile Packaging and Regulatory Compliance

As the VP of Quality Engineering, you must have in-depth knowledge of the sterile packaging industry and regulatory standards such as FDA, ISO, and other relevant certifications. The ideal candidate will possess a deep understanding of the packaging process, quality control systems, and the regulatory requirements that govern sterile product packaging. The ability to ensure full compliance while maintaining operational efficiency is key to this role.

Strategic Thinker with a Focus on Quality Excellence

The client values a strategic leader who can develop and execute long-term quality plans that align with the company’s goals. You should demonstrate the ability to optimize quality processes, minimize waste, and drive innovations in packaging technologies. The ideal candidate will have a proactive approach to quality improvement, with a focus on data-driven decision-making and operational excellence.

Strong Analytical and Problem-Solving Skills

The client is seeking a leader who can analyze complex quality issues, identify root causes, and implement corrective actions effectively. You should possess strong problem-solving abilities and a data-driven mindset, using analytics and performance metrics to monitor and enhance quality processes.

Ability to Build and Lead High-Performance Teams

Leadership is a critical component of this role. The client is looking for someone who can inspire and lead a team of quality engineers, fostering a culture of accountability, collaboration, and continuous learning. You should be able to attract, develop, and retain top talent, ensuring alignment with company objectives while maintaining a focus on performance and development.

Customer-Centric and Stakeholder-Focused

A strong customer-first mindset is essential. The ideal candidate will be able to translate quality assurance insights into actionable improvements that enhance product quality and customer satisfaction. Additionally, you will need to manage key stakeholder relationships, including internal teams, suppliers, and regulatory bodies, ensuring transparency and collaboration.

Commitment to Innovation and Risk Management

The client values a leader who is committed to staying ahead of industry trends, introducing innovative packaging solutions, and proactively managing risks. You should be skilled in identifying potential risks in packaging processes and implementing preventive measures, ensuring both product quality and regulatory compliance are consistently met.

FAQs About the Role – VP of Quality Engineering – Sterile Packaging

What are the key responsibilities of the VP of Quality Engineering in this role?

As the VP of Quality Engineering, you will oversee the quality assurance processes for sterile packaging, ensuring compliance with industry regulations such as FDA and ISO standards. You will be responsible for developing and executing quality strategies, driving continuous improvement initiatives, managing a team of quality engineers, and optimizing packaging operations. Additionally, you will ensure that all packaging processes meet the highest standards of safety, efficiency, and quality while maintaining cost-effective operations.

What qualifications and experience are required for this position?

The ideal candidate should have significant experience in quality engineering, particularly within the sterile packaging or medical device industry. A strong background in implementing quality management systems (QMS), regulatory compliance, and risk management is essential. The client values candidates with a proven track record in leading quality teams, driving process improvements, and ensuring strict adherence to industry regulations. A degree in engineering or a related field is required, and certifications such as Six Sigma or Lean Manufacturing are highly preferred.

What leadership qualities are essential for this role?

The client is seeking a strategic and results-oriented leader with a proven ability to drive quality excellence and operational efficiency. You should possess strong problem-solving skills, the ability to lead cross-functional teams, and a commitment to fostering a culture of continuous improvement. The ideal candidate will be an excellent communicator, able to build relationships with stakeholders, and ensure alignment across various departments while prioritizing quality and compliance.

What challenges can I expect in this role?

As the VP of Quality Engineering, you will face challenges such as maintaining compliance with ever-evolving regulatory standards, optimizing packaging processes to meet demand, and managing risks related to product quality and safety. Additionally, driving continuous improvements across a diverse set of stakeholders and suppliers while maintaining cost efficiency will be key challenges. You must also stay ahead of emerging technologies in sterile packaging to ensure that the company remains competitive in the market.

What is the expected impact of the VP of Quality Engineering on the company’s success?

The VP of Quality Engineering will have a significant impact on the company’s success by ensuring that sterile packaging processes meet the highest quality and regulatory standards. Your leadership in developing and executing quality initiatives will contribute to improving product safety, reducing operational costs, and ensuring customer satisfaction. By driving continuous improvement and fostering a culture of quality, you will help position the company as a leader in the industry.

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

The company values a culture of collaboration, innovation, and excellence. You will be part of a dynamic team that is dedicated to ensuring the highest standards of quality and operational efficiency. The work environment encourages open communication, continuous learning, and cross-functional collaboration to solve complex challenges. You will have the opportunity to lead and shape a high-performance team that is committed to making a lasting impact on the company’s success.

What Remuneration Can You Expect from This Job?

As the VP of Quality Engineering – Sterile Packaging in St. Petersburg, FL, you can expect a highly competitive and comprehensive compensation package that reflects the significant responsibility of this role. The remuneration for this position typically includes:

Base Salary
The base salary for a VP of Quality Engineering in the sterile packaging or medical device industry will depend on the size and complexity of the company, as well as the candidate’s experience. In this role, the annual base salary typically ranges from $150,000 to $250,000, with larger organizations or those with more complex operations offering higher salaries.
Performance-Based Bonuses
In addition to the base salary, many companies offer performance-based bonuses tied to the achievement of key quality metrics, operational efficiency, and successful project completions. These bonuses typically range from 15% to 40% of the base salary, depending on individual and company performance.
Equity & Stock Options
Some companies may offer equity-based incentives, such as stock options or restricted stock units (RSUs). These equity incentives help align the VP’s compensation with the long-term growth and success of the company, offering potential for significant financial gain as the company’s stock value increases.
Profit-Sharing & Long-Term Incentive Plans (LTIPs)
In certain organizations, long-term incentive plans (LTIPs) are available to reward employees for sustained excellence over multiple years. These can be tied to company-wide goals, such as revenue growth, regulatory compliance, or successful product innovations, and typically provide additional financial rewards for long-term contributions.
Executive Benefits & Perks
The VP of Quality Engineering can expect a comprehensive suite of executive benefits, which may include:

Health, dental, and vision insurance
401(k) or pension plans with company contributions
Executive retirement plans
Company-provided vehicle or travel allowances
Wellness programs designed for executives
Expense accounts for business-related activities and travel

Signing Bonuses & Relocation Assistance
For highly sought-after candidates, companies may offer signing bonuses or relocation packages to incentivize candidates to join the organization. These one-time incentives can range from $20,000 to $100,000 or more, depending on the location, candidate’s experience, and the company’s needs.

Total Compensation Potential

When factoring in base salary, performance bonuses, equity incentives, and additional benefits, the total annual compensation for a VP of Quality Engineering in sterile packaging could range from $200,000 to $400,000 or more, depending on company size, industry position, and the individual’s qualifications and performance.

How to Apply

If you are an accomplished leader with extensive experience in quality engineering and sterile packaging, we encourage you to apply for the VP of Quality Engineering – Sterile Packaging position in St. Petersburg, FL. This is an excellent opportunity to lead the quality engineering efforts in a dynamic and high-impact industry, ensuring product excellence, compliance, and continuous improvement in sterile packaging operations.

To apply, please submit the following:

Resume – Highlight your leadership experience in quality engineering, particularly in the sterile packaging or medical device sectors. Showcase your expertise in driving quality systems, ensuring regulatory compliance, and leading cross-functional teams.
Cover Letter – Provide a detailed cover letter outlining your experience in overseeing quality processes, implementing best practices in sterile packaging, managing regulatory affairs, and leading high-performing teams. Demonstrate your ability to drive operational excellence and your strategic approach to quality management.

This is your chance to make a significant impact in a critical role that shapes the future of sterile packaging operations while advancing your career in a leading company. Apply today to take the next step in your executive career as VP of Quality Engineering – Sterile Packaging in St. Petersburg, FL!

For more information or to explore similar opportunities, visit our Quality Engineering Executive Jobs page.

Job Category: Sterile Packaging

Job Type: Full Time

Job Location: St. Petersburg

VP of Quality Engineering – St. Petersburg, FL | Sterile Packaging