QA Documentation Specialist - cGMP Pharma

Smart Media; Manassas (VA); On-site; USD 55,000 - 75,000; Full time

Job summary

Smart Media, located in Manassas, Virginia, is seeking a QA associate for documentation to ensure compliance with cGMP and internal policies. This role involves managing document controls, performing inspections, and ensuring adherence to quality standards.

The ideal candidate should have at least two years of experience in a quality assurance role within a cGMP-regulated environment, along with a relevant degree. Interested applicants can expect fair compensation based on their qualifications and experience.

Qualifications

• At least two years of experience in a quality assurance role in a cGMP-regulated environment.
• Knowledge of cGMP requirements and FDA regulations.

Responsibilities

• Manage and maintain company document control and archival systems.
• Perform inspections and quality system functions in accordance with cGMP.
• Ensure compliance with internal policies and specifications.

Skills

cGMP compliance

Writing documentation

Data analysis

Cross-functional communication

Education

College Degree in Pharmacy, Biology, or Chemistry

Job description

Smart Media, located in Manassas, Virginia, is seeking a QA associate for documentation to ensure compliance with cGMP and internal policies. This role involves managing document controls, performing inspections, and ensuring adherence to quality standards.

The ideal candidate should have at least two years of experience in a quality assurance role within a cGMP-regulated environment, along with a relevant degree. Interested applicants can expect fair compensation based on their qualifications and experience.