In- Process Quality Assurance Technician

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

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.