Description

Perform sampling and testing of incoming raw materials and components in a cGMP laboratory.

This role is on-site.

Responsibilities

• Conduct sampling and testing for raw materials, components, and special projects using various measurement techniques.
• Follow cGMP and 21CFR 820 requirements for all laboratory testing and investigations.
• Adhere to SOPs and established test methods to ensure compliance.
• Manage material flow in coordination with Planning and Scheduling teams.
• Escalate non-conformances and Out of Specification (OOS) results following local and corporate procedures.

Required Skills

• 5+ years of experience in a laboratory or quality control setting.
• Hands-on experience following SOPs.
• Knowledge of cGMP and 21CFR 820 regulations.
• Ability to handle multiple tasks and projects simultaneously.
• Effective verbal and written communication skills.
• Strong interpersonal and team-building abilities.
• Associate’s degree, high school diploma, or equivalent experience.

Preferred Skills

• Experience working in an FDA regulated laboratory.

Key Skills

Education

ANY GRADUATE