Aseptic Quality Assurance Technician (Pharma)

Socket.dev; Fenton (MO); On-site; USD 33,000 - 39,000; Full time

Benefits offered by this job

Employer-paid healthcare coverage

Paid time off

Sick time

401(k) with employer matching

Life insurance

Vision and dental insurance

Parental leave

FSA/HSA options

Education assistance

Job summary

Strive Pharmacy is seeking a Quality Assurance professional to ensure site-specific quality compliance per SOPs, perform document reviews, and assist in release activities. The role focuses on sterile production oversight, environmental monitoring, and sustaining quality records in a fast-paced onsite setting in Fenton, MO.

The ideal candidate has 2+ years in pharma/medical devices quality, aseptic experience, and a background in a regulated environment.

Qualifications

• Minimum High School Diploma or GED with work experience.
• 2+ years in quality or manufacturing in pharma/medical device.
• Experience in aseptic operations and regulated environments.
• Associate degree or higher in technician/science/biology/pharmacy.

Responsibilities

• Inspect products for defects, leaks, and particulates.
• Monitor environmental conditions in sterile areas and document results.
• Assist with media fill processes and unit inspections.
• Review documentation of compounding activities and cleaning records.
• Support equipment calibration programs and maintenance records.
• Assist with raw material release and movement.
• Document deviations and investigations under supervision.
• Support internal and external audits.
• Maintain quality records and participate in quality meetings.

Skills

Quality compliance

Regulatory guidelines

Calculations

Attention to detail

Troubleshooting

Organizational skills

Education

High School Diploma or GED

Associate or higher in technician/biological field

Tools

Sterile manufacturing equipment

Calibration and maintenance records

Job description

Strive Pharmacy is seeking a Quality Assurance professional to ensure site-specific quality compliance per SOPs, perform document reviews, and assist in release activities. The role focuses on sterile production oversight, environmental monitoring, and sustaining quality records in a fast-paced onsite setting in Fenton, MO.

The ideal candidate has 2+ years in pharma/medical devices quality, aseptic experience, and a background in a regulated environment.