Job Description
- Create, develop, maintain, and provide access to the quality management system database.
- Track and resolve user issues and concerns.
- Conducting or assisting with regulatory and quality training sessions.
- Support the development and implementation of improved quality reporting measures.
- Oversight of process change controls.
- Create and revise company standard operating procedures (SOPs) as required.
- Write and train user guidelines and best practices in all aspects of Quality Management Systems.
- Maintain the Organic Certification Program
- Assist in complaint investigations.
- Other duties as assigned by management.
Requirements:
- College degree preferred or equivalent experience.
- 3+ years of experience in manufacturing cGMP environment performing Quality Documentation duties.
- Strong computer skills, including Microsoft Office and databases.
- Must be highly organized and detail oriented. Must be a proactive, self-starter with a results-oriented focus.
- Knowledge and expertise in principles and practice of current Good Manufacturing Practices (GMPs).
- Excellent organizational, verbal, and technical written communication skills.
Job Details:
- Job Type: Full-time.
- Pay: $23.00 - $33.00 per hour.
- Location: Torrance, CA.
Benefits:
- 401(k) matching.
- Dental insurance.
- Health insurance.
- Paid Time Off.
- Vision insurance.