Job Description

Job Title: Quality Assurance Technician – Pharmaceutical Manufacturing

Location: Richmond, KY (100% Onsite)

Duration: 6-Month Contract

Key Responsibilities:

• Monitor production areas to ensure cGMP and FDA compliance
• Review and audit batch records for accuracy and completeness
• Perform in-process testing (particle size, moisture content, bulk density, etc.)
• Conduct visual and AQL inspections of product
• Perform environmental swabbing of cleanrooms and equipment
• Clear rooms and equipment after cleaning is completed
• Identify and resolve production issues in real time
• Initiate and document deviation reports in TrackWise
• Manage product status in inventory systems (e.g., JD Edwards)
• Support investigations and CAPAs
• Train manufacturing staff on documentation and compliance practices
• Assist in complaint investigations by inspecting samples
• Work collaboratively with production, QA, and other departments

Qualifications:

Preferred:

• Bachelor’s degree in a scientific or technical field
• 2+ years of experience in a cGMP-regulated manufacturing environment

Minimum:

• High school diploma with 4+ years of relevant experience

Additional Skills:

• Strong understanding of cGMP, SOPs, and QA practices
• Good communication and teamwork skills
• Experience with TrackWise and JD Edwards is a plus
• Certifications such as Lean Six Sigma or ASQ preferred

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