GMP Documentation & Records Specialist

Integrated Resources Inc.; Richmond (VA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading staffing firm is seeking a Technical Writer with a BS in a scientific field and 1-3 years of experience in the pharmaceutical industry. The role involves preparing compliance documentation, managing electronic records, and ensuring document integrity. Strong writing and communication skills are essential for success in this detail-oriented position.

Qualifications

• Technical writing experience in the pharmaceutical industry preferred.
• 1-3 years of direct experience preferred.
• Advanced knowledge of the Microsoft tool suite required.

Responsibilities

• Prepare analytical and technical documentation in compliance with GMP guidelines.
• Administer electronic document management and maintain records.
• Participate in operations like annual file review and inventory control.

Skills

Writing

Communication

Organizational skills

Attention to detail

Education

BS Degree in Scientific field

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Access

Job description

A leading staffing firm is seeking a Technical Writer with a BS in a scientific field and 1-3 years of experience in the pharmaceutical industry. The role involves preparing compliance documentation, managing electronic records, and ensuring document integrity. Strong writing and communication skills are essential for success in this detail-oriented position.