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 (eg, 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