In-Process QA Specialist — GMP & Manufacturing

Smart Media; Chantilly (VA); On-site; USD 35,000 - 55,000; Full time

Job summary

Granules Pharmaceuticals Inc. in Chantilly, VA is seeking a QA Technician to ensure cGMP compliance on the manufacturing floor. You will monitor environmental conditions, perform water sampling, and support in-process testing and batch documentation.

The role requires attention to detail, strong organizational skills, and the ability to manage multiple priorities as the company grows. Training and SOP adherence are essential in this hands-on quality control position.

Qualifications

• Minimum one to two years in pharmaceutical/food industry with cGMP exposure.
• Experience maintaining cGMP documentation and records.
• Ability to manage multiple priorities and adapt to growth.

Responsibilities

• Perform line clearance, material verification and log book review.
• Collect purified water samples and trend results.
• Coordinate environmental monitoring in GMP areas.
• Review in-process SOPs and batch documentation for gaps.
• Initiate change controls/incidents as needed.
• Maintain employee training records and SOP archival.
• Assist with equipment swab collection, release, and cleanliness checks.
• Perform other duties as assigned by Supervisor.

Skills

cGMP compliance

Document control

Multitasking

Attention to detail

Organization

Education

High School diploma

Associate degree

Job description

Granules Pharmaceuticals Inc. in Chantilly, VA is seeking a QA Technician to ensure cGMP compliance on the manufacturing floor. You will monitor environmental conditions, perform water sampling, and support in-process testing and batch documentation.

The role requires attention to detail, strong organizational skills, and the ability to manage multiple priorities as the company grows. Training and SOP adherence are essential in this hands-on quality control position.