Vice President Quality Assurance

Overview

Job Title:

Vice President, Quality – Pharmaceutical Manufacturing

Location:

Houston, TX

Industry: Pharmaceutical / Biopharmaceutical

Arevna are supporting a rapidly growing pharmaceutical company in Houston, focused on developing and manufacturing high-quality products. We are seeking a hands-on VP of Quality to lead our quality organization and ensure compliance across all regulatory, manufacturing, and operational activities.

The VP of Quality will be a strategic leader and a hands-on operator, responsible for overseeing the full Quality function while actively engaging in day-to-day quality operations. This role requires a deep understanding of GMP, FDA regulations and global quality standards, with a focus on driving quality excellence across manufacturing, supply chain, and product lifecycle.

• Lead and manage all aspects of the Quality organization, including Quality Assurance, Quality Control, and Compliance.
• Ensure full compliance with cGMP, FDA, EMA, and other relevant regulatory requirements.
• Develop, implement, and continuously improve quality systems, policies, and procedures.
• Provide hands-on oversight of batch release, deviations, investigations, and CAPA management.
• Lead internal and external audits and inspections
• Collaborate with R&D, Manufacturing, and Operations to support product development, scale-up, and commercial production.
• Mentor and develop the Quality team, instilling a culture of continuous improvement and operational excellence.

• Minimum 10–15 years of quality leadership experience in pharmaceuticals or biopharmaceuticals.
• Proven experience as a hands-on leader, capable of managing day-to-day quality operations while setting strategic direction.
• Deep knowledge of cGMP, FDA, EMA, ICH, and global regulatory requirements.
• Strong track record of managing regulatory inspections, audits, and product launches.
• Excellent leadership, communication, and problem-solving skills.

• Opportunity to lead a growing, dynamic quality organization.
• Be a key strategic partner in shaping our products and processes.
• Work in a collaborative, fast-paced environment where hands-on leadership is valued.

If you are a strategic yet hands-on Quality leader ready to make an impact in Houston’s pharmaceutical industry, we would love to hear from you.