GMP Quality Control Specialist - On-Site & Documentation

Global Channel Managementinc; Indianapolis (IN); On-site; USD 42,000 - 60,000; Full time

Job summary

Global Channel Managementinc is seeking a Quality Control Representative to support QA, QC, and GMP documentation in a on-site environment in Indianapolis, IN. The role requires experience in QA/QC and the ability to work shifts as needed, including potential weekends.

The candidate should have an Associate degree or equivalent experience and be able to pass a background check and drug screen. Proficiency with MS Office and quality systems is expected.

Qualifications

• Experience in QA, QC, Operations, Engineering or Technical Services.
• Associate degree or equivalent work experience.
• Pass background check and drug screen.
• Ability to work on-site, shifts as needed (morning/afternoon).
• Proficiency with MS Office and quality systems.

Responsibilities

• Maintain physical documentation in GMP areas.
• Perform Good Documentation Practices reviews of GMP documentation.
• Execute audit trail reviews within computer systems per instructions.
• Execute and document quality checks per approved procedures.
• Data entry into computer systems as required.
• Perform other duties as required.

Skills

Quality Assurance

Quality Control

Operations

Engineering

Technical Services

Education

Associate Degree or equivalent

Tools

Microsoft Office

TrackWise

Veeva Quality Docs

Web-based applications

Job description

Global Channel Managementinc is seeking a Quality Control Representative to support QA, QC, and GMP documentation in a on-site environment in Indianapolis, IN. The role requires experience in QA/QC and the ability to work shifts as needed, including potential weekends.

The candidate should have an Associate degree or equivalent experience and be able to pass a background check and drug screen. Proficiency with MS Office and quality systems is expected.