Quality Operations Lead - Packaging & Warehouse

Nephron Pharmaceuticals Corporation; West Columbia (SC); On-site; USD 80,000 - 120,000; Full time

Job summary

Nephron Pharmaceuticals Corporation is seeking an Assistant Manager of Quality Operations for Secondary Packaging & Warehouse to provide quality oversight and leadership across packaging, warehousing, shipping, returns, and related activities.

The role ensures adherence to cGMP, FDA/DEA requirements, and company SOPs, while driving quality improvements, investigations, CAPAs, and documentation accuracy.

Qualifications

• Bachelor’s degree in a scientific, technical, pharmaceutical, engineering, or related field preferred; HS Diploma or GED required.
• Minimum 3 years of pharmaceutical Quality Assurance/Quality Operations experience.
• Secondary packaging, manufacturing, warehouse, distribution, or finished goods experience preferred.
• Minimum 3 years supervisory or lead experience in a GMP environment.
• Experience with deviations, investigations, CAPA, audits, and GMP documentation.

Responsibilities

• Provide Quality oversight for secondary packaging, warehouse, finished goods, shipping, returns, and retain operations.
• Ensure compliance with cGMPs, FDA/DEA requirements, SOPs, safety, and quality systems.
• Monitor packaging operations, line clearances, labeling, documentation, and housekeeping to prevent errors.

Skills

cGMP knowledge

FDA/DEA requirements

Quality Systems

CAPA investigations

Problem solving

Documentation accuracy

Leadership/supervision

Cross-functional teamwork

Microsoft Word/Excel/PowerPoint

Education

Bachelor’s degree in a scientific/engineering field

High School Diploma or GED

Tools

Microsoft Word

Excel

PowerPoint

Electronic Quality Management Systems (eQMS)

Job description

Nephron Pharmaceuticals Corporation is seeking an Assistant Manager of Quality Operations for Secondary Packaging & Warehouse to provide quality oversight and leadership across packaging, warehousing, shipping, returns, and related activities.

The role ensures adherence to cGMP, FDA/DEA requirements, and company SOPs, while driving quality improvements, investigations, CAPAs, and documentation accuracy.