GMP Process Improvement Technician - Biologics

ABBVIE; Ireland; On-site; EUR 42,000 - 65,000; Full time

Job summary

AbbVie in Ireland is seeking a Process Improvement Technician to support production duties including review of logbooks, updating of DtoA vault documents on Vault, generation and inputting of Maximo Production Schedule and supporting gamma irradiation of non-inventory stock.

This role focuses on department change controls and continuous improvements within Core1, coordinating meetings and supporting implementation as required.

Qualifications

• Ability to use sound judgment to make effective decisions within appropriate timeframes.
• Self-directed and able to prioritise competing priorities.
• Excellent planning, organizational, and time management skills.
• Experience with GMP-regulated biologics operations is advantageous.

Responsibilities

• Coordinate, attend & actively participate in meetings to stay aware of tasks assigned to team members and help/support as required.
• Partner with peers to improve efficiencies, brainstorm and troubleshoot issues that arise.
• Vault: generation, review, and approval of assigned documentation. Update BU SOPs.
• GTW: generation and tracking of records and monitoring of Business Unit GTW records daily.
• Generation and inputting of monthly production schedule on Maximo.
• Change control generation, support, and implementation of BU projects.
• Preparation of gamma irradiated non-inventory stock.
• Coordination and preparation of Risk assessments.
• Review and control logbooks as required.
• Manage requirements to deliver project timelines as required.
• Demonstrate active support and involvement in Continuous Improvement initiatives to enhance the operation of the Biologics Business Unit

Skills

Decision making

Self-motivation

Prioritization

Planning

Organization

Stakeholder management

GMP knowledge

Tools

Global TrackWise

Maximo

One Vault

Job description

AbbVie in Ireland is seeking a Process Improvement Technician to support production duties including review of logbooks, updating of DtoA vault documents on Vault, generation and inputting of Maximo Production Schedule and supporting gamma irradiation of non-inventory stock.

This role focuses on department change controls and continuous improvements within Core1, coordinating meetings and supporting implementation as required.