The Document Control QMS Coordinator will be responsible for coordinating, training, performing, and ensuring successful implementation of all areas managed under the QMS program. Ensuring compliance with new and existing quality standards and regulations, implementing quality management actions, and contributing to the development of company policies and procedures. Oversight of document and record lifecycle activities (creation, revision, periodic review, storage, and obsolescence).

• 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.

• 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 Type: Full-time.
• Pay: $2300 - $33.00 per hour.
• Location: Torrance, CA.

• 401(k) matching.
• Dental insurance.
• Health insurance.
• Paid Time Off.
• Vision insurance.