Granules

Vertically integrated API and dosage manufacturer

In-Process Quality Assurance Technician

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeChantilly, VA, USA$19 - $25 /hrIn-person

About the Job

Requirements

A background in current Good Manufacturing Practice (cGMP) compliance within the pharmaceutical manufacturing industry is required.
Experience maintaining cGMP documentation is required.
At least 1 to 2 years of experience in the pharmaceutical or food industry is required.
A high school diploma or associate degree is required.
Ability to manage multiple priorities and reprioritize tasks as required.
Ability to adapt to company growth and evolving responsibilities.
Strong attention to detail and organization.

Responsibilities

Perform line clearance and material verification.
Collect purified water samples for testing and trend the results.
Coordinate environmental monitoring in the Good Manufacturing Practice (GMP) area.
Review logbooks and batch records.
Check equipment cleanliness, collect equipment swabs, and release equipment to operations.
Perform in-process quality assurance testing.
Archive standard operating procedures (SOPs) and batch documentation.
Review in-process SOPs and identify gaps.
Initiate change controls and incident reports.
Maintain employee training records.
Perform other activities as assigned by the supervisor.

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.

About the Company

Granules

Vertically integrated API and dosage manufacturer

Granules India manufactures Active Pharmaceutical Ingredients, Pharmaceutical Formulation Intermediates, and Finished Dosages for customers in more than 80 countries, leveraging large-scale, cost-efficient production. Its vertical integration means it controls the production chain from base chemicals to final packaged medicines, while also marketing its own label products in the US via Granules Pharmaceuticals Inc. The company differentiates itself through a global manufacturing footprint, scale, and an integrated supply chain that supports both contract manufacturing and branded products, including advanced areas like MUPS, oncology, and peptide therapeutics. Its goal is to provide globally accessible, affordable medicines by maintaining secure supply and expanding capabilities in complex therapies, while pursuing sustainability through green chemistry and net-zero emissions.

Company size: 501-1,000
Company stage: Not listed
Total funding: Not listed
Headquarters: Not listed
Founded: 2014

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