Manufacturing Technician – Documentation Support

About the role

AbbVie is seeking an experienced Manufacturing Technician to provide documentation support for its Biologics 2 business unit in Westport. The role focuses on CAPA management, batch documentation, and continuous improvement within a GMP‑controlled environment.

Key responsibilities

• Execute daily tasks assigned by the Senior Operations Manager in compliance with GMP and the quality system.
• Manage batch‑related CAPA activities from initial review through root‑cause analysis, approval, disposition, and implementation of corrective actions.
• Support closure of existing CAPA items by coordinating inter‑departmental actions and ensuring robust preventive measures.
• Lead and contribute to continuous improvement initiatives for the Biologics 2 Process Team.
• Facilitate and generate RCA reports, participate in GEMBA walks and process confirmations to identify improvement opportunities.
• Monitor and deliver KPIs related to product flow and batch release cycles.
• Conduct compliant investigations, handle environmental excursions, and adhere to safety, housekeeping, and gowning procedures.

Required profile

• Proven experience in a GMP‑regulated manufacturing environment.
• Strong understanding of CAPA processes and root‑cause analysis methodologies.
• Ability to work collaboratively across departments and communicate findings clearly.
• Attention to detail and commitment to maintaining high quality and safety standards.

Required skills

• GMP knowledge
• CAPA management
• Root cause analysis (RCA)
• Batch documentation and release procedures
• Continuous improvement techniques