Document Control Coordinator I/II

KBI Biopharma • Boulder, CO

1d • $25 - $35

About The Position

Supports GMP-compliant document control processes by managing controlled documentation, coordinating review and approval workflows, maintaining electronic and paper records, supporting audits and inspections, and ensuring accurate, timely document management for internal stakeholders and clients. The Document Control Coordinator I/II is responsible for managing and maintaining cGMP-controlled documentation throughout its lifecycle, including issuance, review, approval, archival, retrieval, and storage. This role supports manufacturing operations, quality systems, regulatory compliance, and client requirements by ensuring document accuracy, integrity, and accessibility within both electronic and paper-based document management systems. Key responsibilities include issuing manufacturing records, maintaining controlled forms and logbooks, processing documents within the electronic document management system (EDMS), coordinating document review and approval workflows, supporting document archival and off-site storage, responding to documentation requests, and assisting during internal audits, client audits, and regulatory inspections. The position serves as a liaison between internal departments, Quality Assurance, production teams, and clients to ensure timely and compliant document management activities.

Requirements

• Knowledge of document control principles and records management practices.
• Understanding of GMP regulations, quality systems, and data integrity requirements.
• Proficiency with electronic document management systems (EDMS).
• Strong attention to detail and organizational skills.
• Ability to manage multiple priorities and meet deadlines.
• Effective written and verbal communication skills.
• Customer-focused approach with strong service orientation.
• Ability to collaborate effectively across departments and with external clients.
• Problem-solving and continuous improvement mindset.
• Ability to work independently while maintaining accuracy and compliance.
• Document Control Coordinator I: Associate degree in a discipline relevant to document control, quality systems, regulated operations, or equivalent experience.
• Document Control Coordinator I: Typically 1-3 years of experience in document control, quality, records management, or a GMP-regulated environment.
• Document Control Coordinator II: Bachelor's degree in a discipline relevant to document control, quality systems, regulated operations, or equivalent experience.
• Document Control Coordinator II: Typically 3-5 years of experience in document control, quality, records management, or a GMP-regulated environment.
• Document Control Coordinator II: Demonstrated ability to work independently and manage complex document control activities.

Nice To Haves

• Experience with electronic document management systems preferred (for Coordinator I).
• Experience with electronic document management systems required (for Coordinator II).
• Experience supporting audits, inspections, and cross-functional document workflows preferred (for Coordinator II).

Responsibilities

• Manage electronic and paper-based controlled documents throughout their lifecycle, including issuance, review, approval, archival, retrieval, and destruction, as applicable.
• Process and maintain cGMP documentation within the electronic document management system (EDMS).
• Issue manufacturing records and documentation to support production activities.
• Create, issue, maintain, and reconcile controlled forms, logbooks, and related documentation.
• Scan, organize, and archive controlled documents to ensure accurate records retention and retrieval.
• Coordinate document review and approval workflows with internal stakeholders and clients.
• Manage off-site document storage and retrieval activities.
• Fulfill documentation requests from internal and external customers in a timely manner.
• Support internal audits, client audits, and regulatory inspections by providing requested documentation and responding to document control-related inquiries.
• Maintain document accuracy, completeness, and compliance with GMP and company requirements.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree