Biotech Production Coordinator

About the Role

This position is a 1st shift role, Monday-Friday, 8:00 a.m.-4:30 p.m.

Key Responsibilities

• Oversees the lifecycle management of documentation.
• Prepare routine and non-routine progress reports and tracking on various KPIs.
• Maintain inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy.
• Perform and interpret analysis of GMP and GxP data.
• Create and review sampling intake for all manufacturing unit operations and protocols per appropriate documentation prior to operators going on the floor.
• Coordinate appropriate material needs using varying systems and forms to ensure production continuity.
• Ensure systematic bills of materials are created and maintained for production needs.
• Evaluate, initiate, and monitor deviations and other compliance events.
• Coordinate, review, and catalogue various types of manufacturing documentation.
• Serve as a liaison between manufacturing and other functional areas as needed.

Requirements & Tech Stack

• Ability to decipher and navigate a variety of different systems, data, calculations, and documentation.

Qualifications

• BS/BA Degree with 0-2+ years of related experience or equivalent combination of education and experience.
• Experience in a cGMP environment, quality assurance, project management, or inventory management desired.