In- Process Quality Assurance Technician
Granules India
- Location
- Chantilly, VA
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 27
- 1 day ago
Career path
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About the company
Granules India
Pharmaceuticals · 5,001 to 10,000 employees
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.
What you'll do
- Perform line clearance and material verification
- Collect purified water samples for testing and trend the results
- Review log books and batch records
- Check equipment cleanliness, collect equipment swabs, and release equipment
- Perform in-process QA testing
- Initiate change controls and incidents; maintain employee training records
What you need
- Background in cGMP compliance within the pharmaceutical manufacturing industry
- Experience maintaining cGMP documentation
- High school diploma or associate degree
- At least 1 to 2 years’ experience in pharmaceutical or food industry
- 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
Key skills
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