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