Pharma Quality Operations Trainee - GxP Pathway

Allergan; Singapore; On-site; SGD 28,000 - 36,000; Full time

Job summary

AbbVie Singapore invites applications for the Attach & Train Programme, a 15-month structured training path designed to develop skills in quality operations for a regulated biopharmaceutical environment.

As a Training & Document Control Trainee you will work with seasoned professionals, gaining hands-on experience across material control, batch documentation, and product release activities while meeting GxP, quality and compliance standards.

Qualifications

• Bachelor's degree in Science (e.g., Biology or Chemistry) or related field; fresh graduates welcome.
• Familiarity with GxP, quality systems, and quality risk management is a plus.
• Exposure to SAP and TrackWise is advantageous.

Responsibilities

• Support Quality Operations activities to ensure compliance with policies, procedures, and GxP.
• Review incoming material inspection packages, batch records, and QA activities under supervision.
• Assist with release of materials and finished product batches under guidance of QA professionals.
• Participate in investigations related to non-conformances, root-cause analysis, and CAPA implementation.
• Assist with quality data trending and participate in Kaizen and continuous-improvement initiatives.
• Support change-management activities and cross-functional risk assessments with global teams.
• Participate in Product Quality Reviews and quality-system implementation projects.

Skills

Analytical skills

Planning

Organisational skills

Verbal and written communication

Cross-functional collaboration

Attention to detail

Education

Bachelor's degree in Science or related field

Tools

SAP

TrackWise

Job description

AbbVie Singapore invites applications for the Attach & Train Programme, a 15-month structured training path designed to develop skills in quality operations for a regulated biopharmaceutical environment.

As a Training & Document Control Trainee you will work with seasoned professionals, gaining hands-on experience across material control, batch documentation, and product release activities while meeting GxP, quality and compliance standards.