Biotech Manufacturing Coordinator (GMP)

Regeneron Pharmaceuticals, Inc.; Limerick; On-site; EUR 20,000 - 31,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. in Limerick seeks a Biotech Production Coordinator to join the Manufacturing team. The role focuses on coordinating documentation, maintaining inventory accuracy, and acting as a liaison across functions to uphold schedules.

The position requires a BS/BA and 0-2+ years in a related field, with GMP/GxP experience and potential to train staff and lead cross-functional projects.

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.

Responsibilities

• Coordinate, review, and catalogue various types of manufacturing documentation.
• Maintain inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy.
• Serve as a liaison between manufacturing and other functional areas as needed.
• Navigate a variety of systems, data, calculations, and documentation.
• Ensure timelines are met through effective communication with task/project owners.
• Perform analysis of GMP and GxP data.
• Review and approve bills of materials, sample studies, and other manufacturing documentation as needed.
• Extended functional, industry and regulatory knowledge.
• Act as a qualified trainer for new and existing employees.
• Lead and manage projects independently and with cross-functional teams.
• Evaluate, initiate, and monitor deviations and other compliance events.
• Maintain accurate systems related to Manufacturing operations; OPM, MES, LIMS, WMT, FMP, etc.

Education

BS/BA Degree

Job description

Regeneron Pharmaceuticals, Inc. in Limerick seeks a Biotech Production Coordinator to join the Manufacturing team. The role focuses on coordinating documentation, maintaining inventory accuracy, and acting as a liaison across functions to uphold schedules.

The position requires a BS/BA and 0-2+ years in a related field, with GMP/GxP experience and potential to train staff and lead cross-functional projects.