Jobs at AbbVie

Lead and manage biologics manufacturing shifts and teams to meet production, quality, safety, and financial targets. Oversee resource planning, new product introduction, training, budget control, and regulatory inspection readiness. Coach and develop staff, drive cross-functional collaboration, apply technical knowledge to decisions, and implement continuous improvement initiatives.

Support planning and procurement of direct materials for AbbVie Singapore: maintain ERP master data, review MRP outputs, create purchase requisitions, monitor inventory and lead times, support import/export and trade compliance tasks, provide data for supply chain initiatives and audits, and collaborate with cross-functional stakeholders to ensure timely material availability for production.

Manage the sales territory to achieve sales targets, while identifying new business opportunities and maintaining customer relationships. Duties include organizing records, delivering presentations, and collaborating with cross-functional teams.

The Senior Manager, Regulatory Affairs leads JAPAC regulatory initiatives, liaises with affiliate teams, ensures compliance with local regulations, and manages health authority interactions for therapeutic areas including Neuroscience and Eyecare.

The Risk and Analytics Regional Insights Manager will drive data-driven risk management capabilities across the JAPAC region, serving as a liaison between compliance teams and promoting the use of analytics for insight generation and decision-making.

Performs cGMP manufacturing operations in a biologics facility, focusing on purification processes, data entry, and leading troubleshooting efforts.

The Associate Director, IT will drive business-IT strategy, develop technology roadmaps, ensure compliance, manage budgets, and lead cross-functional teams in digitalization efforts.

Lead and oversee the Manufacturing Support function for biologics operations, ensuring compliance, quality, training, and operational readiness across teams.

The Head of Compliance oversees AbbVie's compliance program in Pharmaceuticals across Singapore, Malaysia, and Thailand, including development of training, risk assessments, and partnerships with local teams to ensure adherence to regulations.

The Validation Engineer II is responsible for cleaning validation plans, ensuring compliance with GMP standards, generating protocols, and coordinating validation activities in API and Biologics manufacturing facilities.

This role supports QC operations in a biotech setting, ensuring compliance with standards, managing documentation, and facilitating new product introduction.

The Senior Security Analyst I leads identity lifecycle events, governance activities, and access provisioning, ensuring compliance with security frameworks. They drive improvements and collaborate with teams to enhance IAM operational reliability and documentation for audits.