Quality Control Manager

Turbare Manufacturing LLC • Conway, AR

7h

About The Position

Turbare Manufacturing is a leading sterile compounding facility dedicated to providing high-quality pharmaceutical products in compliance with all regulatory standards. We are seeking a detail-oriented and experienced Quality Control Manager to oversee our quality assurance processes, ensuring the safety, efficacy, and regulatory compliance of our sterile compounded products. Join our team and contribute to our mission of delivering safe and reliable medications to patients.

At Turbare Manufacturing, we are committed to fostering a collaborative and innovative work environment. We offer opportunities for professional growth, competitive benefits, and the chance to make a meaningful impact on patient health through our high-quality pharmaceutical products.

Requirements

• Bachelor’s degree in Pharmacy, Chemistry, Microbiology, or a related scientific field; advanced degrees preferred.
• Minimum of 5 years of experience in quality control within a sterile compounding or pharmaceutical manufacturing environment.
• In-depth knowledge of 503B regulations, cGMP, USP standards, and sterile compounding practices.
• Strong leadership and team management skills.
• Excellent analytical, problem-solving, and communication skills.
• Experience with quality management systems (QMS) and laboratory instrumentation.
• Ability to interpret complex regulatory requirements and implement compliant procedures.

Responsibilities

• Develop, implement, and maintain quality control procedures and protocols in accordance with FDA 503B regulations and industry standards.
• Oversee the daily operations of the quality control laboratory, including testing, inspection, and documentation of raw materials, in-process samples, and finished products.
• Ensure compliance with all applicable regulatory requirements, including cGMP, USP standards, and other relevant guidelines.
• Lead investigations into quality issues, deviations, and complaints, implementing corrective and preventive actions (CAPA).
• Manage and train quality control staff, fostering a culture of continuous improvement and compliance.
• Collaborate with production, regulatory affairs, and other departments to ensure quality standards are integrated into all processes.
• Prepare and review quality documentation, reports, and audit responses for internal and external inspections.
• Monitor and trend quality data to identify areas for process improvement and risk mitigation.

Benefits

• opportunities for professional growth
• competitive benefits
• chance to make a meaningful impact on patient health through our high-quality pharmaceutical products

What This Job Offers

• Job Type: Full-time
• Career Level: Manager