In- Process Quality Assurance Technician

Granules India

Chantilly, VAOn-siteFull time
With an account: save jobs, track applications, build tailored resumesAlready have an account? Log in
Location
Chantilly, VA
Work style
On-site
Job type
Full time
Posted
Oct 27
1 day ago
Career path

See where this role leads

Jigup maps the next three moves from a job like this one, with the titles and the skills each step asks for.

Create an account

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.

Granules India on LinkedIn

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

cGMP compliancecGMP documentationManage multiple prioritiesAttention to detailOrganization

Keywords for your resumePro

The words this employer's screening is likely to look for.

This job lists resume keywords

The terms this posting uses, pulled out so you can mirror them in your resume. Jigup Pro members see the list on the job board.

Create an account

See full description on company page, apply now

Read the full posting here
Apply 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.

More entry level jobs in Chantilly, VA

All jobs in Chantilly, VA

More jobs at Granules India

Ready to apply?

Create an account to save jobs, track applications, and build tailored resumes.

Create an account