Manager Of Quality

Manager of Quality – San Angelo, TX

Relocation assistance available

We are seeking an experienced Quality Manager to oversee Quality Assurance (QA) and Quality Control (QC) operations at our San Angelo, Texas manufacturing site. This leader will be responsible for ensuring all products and processes meet applicable regulatory standards while championing continuous improvement and a strong quality culture throughout the facility.

This role is ideal for a hands-on, collaborative manager who excels in regulated environments and is passionate about driving quality excellence through systems, data, and cross-functional partnership.

Key Responsibilities

Quality Assurance

• Lead the maintenance, enhancement, and overall effectiveness of the site’s Quality Management System.
• Interpret evolving regulatory requirements and communicate compliance expectations across the organization.
• Develop, refine, and enforce practical quality procedures aligned with industry and legal standards.
• Track, analyze, and present key quality metrics to leadership.
• Guide teams in meeting quality standards and expectations.
• Manage batch release processes and ensure all associated documentation is accurate and complete.
• Oversee controlled documentation, including SOPs, deviations, CAPAs, and complaints.
• Direct root cause investigations and verify implementation of corrective and preventive actions.
• Lead internal/external audits and ensure timely closure of findings.
• Serve as the primary liaison for audits, regulatory inspections, and customer quality inquiries.
• Foster a mindset of inspection readiness and continuous improvement.

Quality Control

• Oversee laboratory testing activities that support manufacturing, batch release, and stability programs, ensuring accuracy, compliance, and on-time delivery.
• Implement and sustain QC processes, including method development, validation, transfer, and analytical lifecycle management.
• Maintain high standards for documentation, data integrity, and audit readiness across all QC workstreams.
• Ensure proper calibration, qualification, and maintenance of laboratory equipment.
• Lead cross-functional activities related to investigations, specification setting, stability programs, and reference standard management.
• Support regulatory filings through review and preparation of analytical documentation.
• Train and mentor QC staff while identifying opportunities to enhance laboratory efficiency and performance.

Competencies

Effective Communication – Ability to communicate clearly, listen actively, validate understanding, and convey information with accuracy and professionalism across teams and levels.

Relationship Building – Skilled in developing positive working relationships that support credibility, trust, and long-term collaboration.

Leadership – Capable of inspiring teams, setting direction, promoting accountability, and reinforcing a high‑performance culture aligned with organizational values.

Analytical Thinking & Problem Solving – Adept at identifying key information, analyzing data, recognizing patterns, and applying structured methods to resolve complex issues.

Engagement, Drive & Empowerment – Demonstrates confidence in team capabilities, delegates effectively, and encourages autonomy in pursuit of goals.

Qualifications

• Bachelor’s degree in Biology, Microbiology, or a related scientific discipline required.
• Advanced degree (MS or PhD) preferred.
• 7 years of experience in QA, QC, or related quality functions within pharmaceutical or biotech manufacturing.
• At least 3 years of leadership or supervisory experience strongly preferred.
• Strong knowledge of GMP, USDA regulations, and quality systems.

What You Bring

• Proven leadership, communication, and decision-making skills.
• Experience managing audits, inspections, and regulatory interactions.
• Strong understanding of documentation systems and quality lifecycle management.
• Detail-oriented approach with a commitment to accuracy, compliance, and continuous improvement.

Job Type & Location

This is a Permanent position based out of San Antonio, TX.

The pay range for this position is $100000.00 - $120000.00/yr.

Bimeda: New benefits meetings underway. They have had cost decrease and coverage increase several times now

This is a fully onsite position in San Antonio,TX.

This position is anticipated to close on Mar 12, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $100,000 - $120,000