QA Document Control Specialist, cGMP Records

TechDigital Group; Bothell (WA); On-site; USD 60,000 - 90,000; Full time

Job summary

An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP operations. In this role, you will be responsible for managing GMP records, ensuring compliance with regulatory standards, and facilitating the document approval process. The ideal candidate will have a strong background in document control within regulated environments and possess excellent communication and project management skills. Join a dynamic team where your contributions will enhance quality and efficiency in a fast-paced setting, making a significant impact on the organization's success.

Qualifications

• 5-8 years of experience in document control within cGMP/FDA environments.
• Strong computer skills and proficiency in MS Office and Quality Systems.

Responsibilities

• Organize cGXP controlled document files for easy retrieval.
• Manage the Document Center Archive room and ensure compliance.

Skills

Document Control Management

Communication Skills

Customer Service Skills

Project Management

cGMP Knowledge

Problem Solving

Education

Bachelor's Degree

Library Science

Tools

MS Office

Document Management System

Quality Management System

Adobe

Visio

Excel

Job description

An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP operations. In this role, you will be responsible for managing GMP records, ensuring compliance with regulatory standards, and facilitating the document approval process. The ideal candidate will have a strong background in document control within regulated environments and possess excellent communication and project management skills. Join a dynamic team where your contributions will enhance quality and efficiency in a fast-paced setting, making a significant impact on the organization's success.