QUALITY ENGINEER at NEPHRON SC, LLC

West Columbia, South Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

07 Jul, 26

Salary

0.0

Posted On

08 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Cgmp, Aseptic manufacturing, Facility commissioning, Process improvement, Cleanroom operations, Root cause analysis, CAPA, Data integrity, Technology transfer, Validation, Process automation, Risk assessment, Documentation, Quality systems, Regulatory compliance, Smoke studies

Industry

Pharmaceutical Manufacturing

Description

Description 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. Essential Duties and 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 Requirements Education / Experience: · 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. · Experience with commissioning/startup activities, cleanroom and contamination control practices (including smoke studies), process automation systems, validation, and cGMP/FDA regulatory requirements preferred. Working Conditions / Physical Requirements: · Position requires bending (desk to floor), lifting (up to 15 lbs.), corrected vision (20/20), standing, sitting, typing, and walking. · Ability to work in cleanroom environments, including gowning requirements.

Responsibilities

The Quality Engineer supports aseptic manufacturing operations by executing quality system activities and participating in facility and equipment commissioning. They collaborate cross-functionally to ensure cGMP compliance while driving process improvements and supporting technology transfer.