Pharma Visual QA Inspector — Packaging

Nephron Pharmaceuticals Corporation

West Columbia (SC)

On-site

USD 38,000 - 52,000

Full time

5 hours ago
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Job summary

Nephron Pharmaceuticals Corporation seeks a QA Visual Inspection associate to ensure quality attributes during packaging and maintain batch-record accuracy. The role involves monitoring cGMP/SOP adherence and performing line clearances.

Responsibilities include supporting validation studies, releasing products after inspection, and cross-training across QA and production departments to broaden expertise.

Qualifications

  • High School Diploma or GED.
  • Minimum of 1 year pharmaceutical QA/Production experience preferred.
  • Knowledge of GMP is preferred.
  • Detail oriented with strong observation skills.

Responsibilities

  • Perform Quality Attributes and Visual Inspection of drug product through the packaging process per FDA and cGMP regulations.
  • Ensure the accuracy and completeness of manual and electronic batch records.
  • Monitor packaging areas and personnel for adherence to cGMP, SOPs and safety regulations.
  • Perform line clearance including equipment, components and label verification.
  • Support validation and manufacturing studies including sampling and testing.
  • Release finished product for packaging after visual inspection.
  • Review batch records to ensure completion and Good Documentation Practices.
  • Cross-train in other departments to expand job knowledge.

Skills

Detail oriented
Visual acuity
Observation skills
Written communication
Oral communication
Teamwork
GMP knowledge

Education

High School Diploma or GED

Tools

MS Outlook
MS Word
MS Excel

Job description

Nephron Pharmaceuticals Corporation seeks a QA Visual Inspection associate to ensure quality attributes during packaging and maintain batch-record accuracy. The role involves monitoring cGMP/SOP adherence and performing line clearances.

Responsibilities include supporting validation studies, releasing products after inspection, and cross-training across QA and production departments to broaden expertise.

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