QUALITY ENGINEER

NEPHRON SC, LLC • West Columbia, SC

4d

About The Position

Job Purpose:
The Quality Engineer supports aseptic manufacturing operations by executing quality system activities, participating in facility and equipment commissioning, and driving process improvements. This role works cross-functionally with Manufacturing, Engineering, MS&T, and Quality to ensure compliance with cGMP requirements while supporting both development and commercial manufacturing programs.
This position includes hands-on involvement in cleanroom environments and requires strong technical, analytical, and documentation skills.

Requirements

• Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or a related field.
• 2-5 years of experience in pharmaceutical manufacturing or a related industry, with a strong understanding of pharmaceutical processes and GMP.

Nice To Haves

• Experience with commissioning/startup activities, cleanroom and contamination control practices (including smoke studies), process automation systems, validation, and cGMP/FDA regulatory requirements preferred.

Responsibilities

• Execute and support cGMP operations and project-based work, including commissioning activities, process studies, and quality system initiatives
• Participate directly in facility and equipment commissioning activities, including field execution, documentation, and coordination with engineering and operations teams
• Support and execute process and product development studies, including data collection, analysis, and documentation
• Contribute to technology transfer and scale-up activities, supporting successful transition from development to manufacturing
• Participate in cleanroom and controlled environment activities, including:
• Supporting airflow visualization (smoke studies)
• Assisting with cleanroom setup, readiness, and operational support
• Execute and support CAPA-related projects, including root cause analysis, implementation of corrective and preventive actions, and effectiveness checks
• Support deviations, investigations, and change controls through data gathering, documentation, and implementation of actions
• Ensure all work is documented in accordance with cGMP requirements, maintaining accuracy, completeness, and data integrity
• Collaborate cross-functionally with Manufacturing, Engineering, MS&T, and Quality teams to support facility startup, operational readiness, and continuous improvement initiatives
• Participate in risk assessments and support mitigation activities related to processes, equipment, and cleanroom environments
• Contribute to inspection readiness efforts, including documentation support and response to audit observations
• Identify and support process and operational improvements across development and manufacturing activities

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 251-500 employees