Quality Control Technician

Job Description

Job Description

Description :

About Turbare Manufacturing :

Turbare Manufacturing is a leading FDA-registered 503B outsourcing facility focused on providing safe, compliant, and reliable compounded sterile medications to healthcare institutions nationwide. We are committed to rigorous quality oversight and adherence to regulatory expectations to ensure patient safety and product integrity. Our guiding principle, “Only The Best Will Do,” reflects our dedication to excellence in all aspects of our operations.

Position Summary :

Turbare Manufacturing, a leading 503B outsourcing facility, is seeking a qualified detail-oriented Quality Control Technician to support its sterile compounding operations. The Quality Control Technician will be responsible for performing sampling, testing, documentation, and quality verification activities to ensure products meet established specifications and are manufactured in accordance with applicable regulatory and cGMP requirements.

Essential Duties and Responsibilities :

The essential functions of this position include, but are not limited to the following :

• Conduct routine environmental monitoring to assess the cleanliness and control of the compounding areas. This includes air sampling, surface sampling, and non-viable particulate monitoring to identify any potential sources of contamination.
• Perform environmental and personnel monitoring sample collection, incubation and enumeration (plate count) processes.
• Assist with qualification activities for cleanroom personnel and aseptic processes e.g. gowning qualifications and media fill qualifications.
• Accurately document and report test results, ensuring timely completion of records in accordance with data integrity and GDP requirements.
• Identify and investigate deviations, non-conformances, and quality issues, and collaborate with cross-functional teams to implement corrective and preventive actions.
• Participate in the validation and qualification of equipment, processes, and analytical methods.
• Assist in the development and revision of standard operating procedures (SOPs) related to quality control activities.
• Contribute to continuous improvement initiatives aimed at enhancing product quality, efficiency, and compliance.
• Adhere to good manufacturing practices (GMP), safety protocols, and quality system requirements at all times.
• Support internal and external audits, inspections, and regulatory submissions as needed.
• Maintain current knowledge of applicable regulatory expectations, industry guidelines, and best practices relevant to pharmaceutical quality control.

Benefits :

Turbare Manufacturing is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Turbare Manufacturing’s at-will employment statement : “Employment at Turbare Manufacturing is at-will, meaning either the employee or the company may terminate the employment relationship at any time, with or without cause or notice, as permitted by law.”

Requirements :

Physical Demands and Work Environment

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodation may be made to enable individuals with disabilities to perform the functions.

Minimum Qualifications (Knowledge, Skills, and Abilities)