QA Documentation & Compliance Specialist (cGMP)

Granules Pharmaceuticals Inc.; Manassas (VA); On-site; USD 60,000 - 80,000; Full time

Job summary

Granules Pharmaceuticals Inc. in Manassas, Virginia is looking for a QA Associate focused on documentation compliance with cGMP standards. Responsibilities include managing document control systems, supporting inspections, and training new hires in GMP and safety protocols.

The ideal candidate will have at least two years of experience in a quality assurance role and a college degree in a relevant field such as Pharmacy or Biology. This position is essential for ensuring product quality and regulatory compliance.

Qualifications

• At least two years’ experience in a quality assurance role in a cGMP-regulated environment.
• A college Degree preferably in Sciences (i.e. Pharmacy, Biology, Chemistry etc.).

Responsibilities

• Manage and maintain document control and archival systems.
• Perform inspections and batch record review for compliance.
• Provide new hire training on GMP's, Safety, and Pharmacovigilance.

Skills

cGMP compliance

Writing cGMP documentation

Data analysis

Communication skills

Team collaboration

Task prioritization

Education

College Degree in Sciences

Job description

Granules Pharmaceuticals Inc. in Manassas, Virginia is looking for a QA Associate focused on documentation compliance with cGMP standards. Responsibilities include managing document control systems, supporting inspections, and training new hires in GMP and safety protocols.

The ideal candidate will have at least two years of experience in a quality assurance role and a college degree in a relevant field such as Pharmacy or Biology. This position is essential for ensuring product quality and regulatory compliance.