In-Process QA Specialist – Pharma Manufacturing

Granules Pharmaceuticals; Chantilly (VA); On-site; USD 42,000 - 65,000; Full time

Job summary

Granules Pharmaceuticals is seeking a QA Technician to ensure cGMP compliance on the manufacturing floor in Chantilly, VA. You will perform line clearance, collect water samples, monitor environmental conditions, and review batch records to uphold quality standards.

The role requires 1–2 years of experience in pharmaceutical/food environments and a High School diploma or Associate degree. You will maintain training records and assist with SOP archival and change controls as needed.

Qualifications

• Background in cGMP compliance within pharmaceutical manufacturing.
• Experience maintaining cGMP documentation.
• Ability to manage multiple priorities and re-prioritize tasks.
• Flexible and able to adapt to company growth and evolving responsibilities.
• Strong attention to detail and excellent organization.

Responsibilities

• Perform line clearance, material verification.
• Collect purified water sample for testing, Trending the results.
• Coordinate Environmental monitoring in GMP area.
• Log book and Batch record review.
• Check equipment cleanliness and Swab collection, Equipment release to the operations.
• In process QA testing.
• Archival of SOPs, Batch documentation.
• Review the In-process SOPs and identify the gaps.
• Initiation of Change control/Incidents.
• Maintain the employee training records.
• Perform Any other activity as assigned by the Supervisor.

Skills

cGMP compliance

Documentation

Prioritization

Attention to detail

Organization

Education

High School diploma/Associate degree

Job description

Granules Pharmaceuticals is seeking a QA Technician to ensure cGMP compliance on the manufacturing floor in Chantilly, VA. You will perform line clearance, collect water samples, monitor environmental conditions, and review batch records to uphold quality standards.

The role requires 1–2 years of experience in pharmaceutical/food environments and a High School diploma or Associate degree. You will maintain training records and assist with SOP archival and change controls as needed.