Pharma QA Technician — On-Site Quality & Compliance

Strive pharmacy; Leesburg (VA); On-site; USD 33,000 - 39,000; Full time

Benefits offered by this job

Healthcare benefits

Paid time off

401(k) with employer matching

Life insurance

Vision and dental insurance

Job summary

Strive Pharmacy is a personalized compounding pharmacy seeking a Quality Assurance professional to ensure site-specific quality compliance and assist with release activities.

Responsibilities include product inspections, environmental monitoring, documentation review, and supporting audits. Requires at least a high school diploma and 2 years in a quality/manufacturing environment within pharma or medical devices.

Qualifications

• Minimum of a High School Diploma or GED with work experience.
• Minimum of 2 years experience in a quality or manufacturing department of a Pharmaceutical, Medical Device, or Allied Health Science.

Responsibilities

• Perform product inspection for defects, leaks, and particulates.
• Environmental monitoring of personnel (as needed) and complete documentation.
• Assist in media fill process validations to include inspection of filled units.
• Perform documentation review of compounding activities such as cleaning records, line clearance forms, and inventory sheets.
• Verify that raw materials meet specification
• Account for labeling
• Review temperature and BMS alarms
• Ensure that product test results meet specification limits
• Document non-compliance and work with supervisor/lead as needed for investigations
• Support internal & external audits
• Maintain quality records (calibration, maintenance, training, deviations, environmental monitoring, COA, clean room certification)
• Participate in Quality Manager's staff meetings

Skills

Quality Assurance

Documentation

Inspection

Calibration

GMP

Education

High School Diploma or GED

Associate degree or higher

Tools

Calibration tools

Documentation systems

Job description

Strive Pharmacy is a personalized compounding pharmacy seeking a Quality Assurance professional to ensure site-specific quality compliance and assist with release activities.

Responsibilities include product inspections, environmental monitoring, documentation review, and supporting audits. Requires at least a high school diploma and 2 years in a quality/manufacturing environment within pharma or medical devices.