The primary purpose of this position is to support and perform documentation administration activities within the Quality function, adhering to Good Manufacturing Practices (GMP) and Quality system guidelines
Job Summary
The primary purpose of this position is to support and perform documentation administration activities within the Quality function, adhering to Good Manufacturing Practices (GMP) and Quality system guidelines.
Adhere to company policies and procedures and all safety and quality requirements including, but not limited to: Quality Management Systems (QMS), Environmental and Security Management Systems (EMS), U.S. Food and Drug Administration (FDA) regulations.
Grow on the job and help others succeed, expanding your skill base through on-the-job training, cross training, and classroom instruction.
Matching Summary
The primary purpose of this position is to support and perform documentation administration activities within the Quality function, adhering to Good Manufacturing Practices (GMP) and Quality system guidelines.
Skills & Requirements
Must-have
Quality Management Systems
Good Manufacturing Practices
Good Documentation Practices
Electronic documentation systems
Document control and distribution
Nice-to-have
Leadership by example
Cross-training and skill expansion
Driving process quality improvements
Living company values
Key Requirements
2-3 years of experience
High school graduate or equivalent
Working knowledge of Electronic documentation systems
Understanding of Quality Management Systems (e.g., ISO9001, ISO13485, FDA 21CFR Part 820)