In- Process Quality Assurance Technician

Granules Pharmaceuticals, Inc.; Chantilly (VA); On-site; USD 52,000 - 68,000; Full time

Job summary

Granules Pharmaceuticals, Inc. (GPI) in Chantilly, VA, is seeking a QA Technician to monitor the manufacturing floor, collect water samples, and ensure SOP compliance. The role supports cGMP practices, line clearance, and batch documentation review within our controlled environment.

Responsibilities include environmental monitoring coordination, swab collection, equipment release, and archival of SOPs. Candidates should have 1–2 years in pharma/food or related industries and strong attention to

Qualifications

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

Responsibilities

• Perform line clearance, material verification
• Collect purified water sample for testing, trending results
• Coordinate environmental monitoring in GMP area
• Log books and batch record review
• Check equipment cleanliness and swab collection, equipment release to operations
• In-process QA testing
• Archiv​​al of SOPs and batch documentation
• Review in-process SOPs and identify gaps
• Initiation of change control/incidents
• Maintain employee training records
• Perform any other activity as assigned by Supervisor.

Skills

cGMP compliance

Documentation management

Multitasking

Attention to detail

Education

HS diploma or Associate degree

Job description

Job Type

Full-time

Description

Granules Pharmaceuticals Inc., (GPI) has worked towards strengthening our core for the past 40 years and is currently the 4th largest generic pharma company in the US for controlled substances!
With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.
We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.
The QA Technician compliance with cGMP and SOP’s and systems. This position is responsible for daily floor monitoring., water sampling for testing, swab collection. In-process testing, line clearance. Monitor manufacturing personnel follow and adhere to SOP pertaining to Manufacturing floor activities.

Job Description/Responsibilities

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

Requirements

• A background in cGMP compliance within the pharmaceutical manufacturing industry is required.
• Experience in maintaining cGMP documentation.
• Ability to manage multiple priorities and re-prioritize tasks, as required.
• Flexible and able to adapt to company growth and evolving responsibilities
• Strong attention to detail and excellent organization

Minimum Education/Experience

• High School diploma, or Associate degree.
• At least 1 to 2 years’ experience in pharmaceutical/food industry

We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.