Quality Ops Specialist II: Systems & Improvement

AbbVie; Singapore; On-site; SGD 80,000 - 110,000; Full time

Job summary

AbbVie Singapore is seeking a Quality Operations Specialist to support site management in overseeing the quality system across manufacturing and production areas. The role requires documenting, monitoring, and reporting quality issues, leading quality improvement projects, and ensuring released batches meet regulatory and company standards.

You will perform audits of incoming materials, execute QA holds, release batches, and drive data trending and kaizen initiatives with cross-functional teams.

Qualifications

• Minimum 3+ years of pharmaceutical quality/compliance experience.
• 0
• Knowledge of quality systems and regulatory requirements (GxP).
• Experience with SAP and TrackWise is preferred.
• Strong documentation and data-trending abilities.
• Excellent communication and cross-functional collaboration.

Responsibilities

• Ensure AbbVie Singapore products meet policies and procedures.
• Oversee incoming materials quality and processes.
• Lead investigations into non-compliance and implement CAPA.
• Perform QA data trending and Kaizen for improvements.
• Coordinate change management and cross-functional risk assessments.
• Release batches and conduct quality reviews.
• Conduct regular walk-throughs to ensure ongoing compliance.
• Assist site management in quality system execution.

Skills

Quality systems

GxP compliance

Root cause analysis

Process improvement Kaizen

Change management

Data trending

Project management

Cross-functional teamwork

Communication skills

Education

Bachelor Degree in Sciences

Tools

SAP

TrackWise

Job description

AbbVie Singapore is seeking a Quality Operations Specialist to support site management in overseeing the quality system across manufacturing and production areas. The role requires documenting, monitoring, and reporting quality issues, leading quality improvement projects, and ensuring released batches meet regulatory and company standards.

You will perform audits of incoming materials, execute QA holds, release batches, and drive data trending and kaizen initiatives with cross-functional teams.