GMP Documentation QA Specialist

Granules Pharmaceuticals, Inc.; Manassas (VA); On-site; USD 55,000 - 75,000; Full time

Job summary

Granules Pharmaceuticals, Inc. is looking for a QA Associate in Manassas, Virginia. This role involves ensuring compliance with cGMP regulations while managing document control systems and supporting quality assurance functions. The ideal candidate has at least two years of experience in a quality assurance role and a college degree in a related science field.

Key responsibilities include performing batch record reviews, collaborating with teams, and maintaining documentation training. Applicants should have strong communication skills and the ability to prioritize tasks effectively.

Qualifications

• 2+ years experience in a quality assurance role in a cGMP-regulated environment.
• Strong understanding of cGMP requirements and FDA regulations.
• Ability to analyze data and resolve complex issues.

Responsibilities

• Manage and maintain document control and archival systems.
• Perform inspections and batch record reviews.
• Provide training on GMPs and maintain documentation.

Skills

cGMP compliance

Documentation writing

Data analysis

Verbal communication

Team collaboration

Task prioritization

Education

College degree in Sciences (Pharmacy, Biology, Chemistry)

Job description

Granules Pharmaceuticals, Inc. is looking for a QA Associate in Manassas, Virginia. This role involves ensuring compliance with cGMP regulations while managing document control systems and supporting quality assurance functions. The ideal candidate has at least two years of experience in a quality assurance role and a college degree in a related science field.

Key responsibilities include performing batch record reviews, collaborating with teams, and maintaining documentation training. Applicants should have strong communication skills and the ability to prioritize tasks effectively.