In-Process Quality Technician: GMP Compliance & Line Testing

Granules Pharmaceuticals Inc.; Chantilly (VA); On-site; USD 45,000 - 65,000; Full time

Job summary

Granules Pharmaceuticals Inc. in Chantilly, VA, seeks a QA Technician to support cGMP compliance on the manufacturing floor. You will perform line clearance, water sampling, environmental monitoring, and in-process QA testing.

Responsibilities include record review, equipment swab collection, batch documentation, training records, and initiating change controls. Minimum 1–2 years in pharma/food, HS or associate degree, strong attention to detail.

Qualifications

• Background in cGMP compliance within pharmaceutical manufacturing.
• Experience maintaining cGMP documentation.
• Ability to manage multiple priorities with attention to detail.

Responsibilities

• Perform line clearance, material verification.
• Collect purified water samples for testing; trend results.
• Coordinate environmental monitoring in GMP areas.
• Log books and batch review.
• Check equipment cleanliness; collect swabs; release equipment to operations.
• In-process QA testing; archival of SOPs and batch docs.
• Review in-process SOPs and identify gaps; initiate changes.
• Maintain employee training records; perform other supervisor-assigned tasks.

Skills

cGMP compliance

Documentation

Quality monitoring

Education

High School or Associate degree

Job description

Granules Pharmaceuticals Inc. in Chantilly, VA, seeks a QA Technician to support cGMP compliance on the manufacturing floor. You will perform line clearance, water sampling, environmental monitoring, and in-process QA testing.

Responsibilities include record review, equipment swab collection, batch documentation, training records, and initiating change controls. Minimum 1–2 years in pharma/food, HS or associate degree, strong attention to detail.