QA Document Control Coordinator

Biotechnology/Pharmaceutical company focusing on life science seeking QA Document Control Coordinator . This will be responsible for managing the daily Quality Assurance documentation and supporting the integrity of our Quality Management System (QMS) to ensure compliance and operational excellence.

Key Responsibilities

• Analyze & Set Objectives: Establish, monitor, and procure goals and objectives related to Quality Assurance.
• Problem Solving: Troubleshoot and resolve any quality-related issues that may arise during daily operations.
• QMS & Documentation Monitoring: Oversee QA activities including training records, Standard Operating Procedures (SOPs), Batch Records (SOPBRs), QMS documents, change controls, and customer feedback.
• Compliance Support: Diligently follow and support all established procedures within the Quality Management System.
• Training Management: Manage employee training tracking and documentation within their assigned roles.
• Document Control: Review, revise, update, and create new documents, SOPs, and SOPBRs as needed.
• Equipment Oversight: Monitor equipment status and maintenance schedules.
• Shipment Review: Perform reviews of outbound shipments to meet quality standards.
• Regulatory Awareness: Stay current on industry quality issues, regulations, and developments affecting quality assurance.
• Cross-Functional Duties: Perform other assigned tasks both within and outside the department as needed.

Minimum Qualifications

• Education: Associate degree in science discipline or a related field.
• Experience: Previous professional experience within a documentation role.
• Technical
  
  Skills:
  
  Strong computer literacy, particularly with Microsoft Word and Excel.
• Personal Attributes: Highly organized, capable of working independently, and exceptionally detail oriented.