QA Report Generation Specialist — GMP & Documentation

Agupdate; Wilmington, Northern (NC, KY); Hybrid; USD 55,000 - 75,000; Full time

Benefits offered by this job

Excellent benefits

Career advancement

Childcare facility

Job summary

Quality Chemical Laboratories (QCL) in Wilmington, NC, is seeking a QA Associate – Report Generation to join our quality team. The role focuses on reviewing and approving reports generated from laboratory data, including certificates of analysis and stability tables, ensuring accuracy and GMP/SOP compliance.

The successful candidate will demonstrate meticulous documentation, strong communication, and problem-solving skills.

Qualifications

• Experience in quality assurance workflows within pharma labs.
• Ability to review reports for GMP and SOP compliance.
• Strong documentation and formatting skills.
• Attention to detail and organized approach.

Responsibilities

• Review and approve reports generated from laboratory data.
• Verify certificates of analysis and stability tables for accuracy.
• Assist with method verifications and validations as needed.
• Format documents to meet GMP/SOP standards and maintain records.

Skills

Quality Assurance

Documentation

Report Generation

GMP Compliance

Word Proficiency

Tools

Microsoft Word

Job description

Quality Chemical Laboratories (QCL) in Wilmington, NC, is seeking a QA Associate – Report Generation to join our quality team. The role focuses on reviewing and approving reports generated from laboratory data, including certificates of analysis and stability tables, ensuring accuracy and GMP/SOP compliance.

The successful candidate will demonstrate meticulous documentation, strong communication, and problem-solving skills.