Jobs at AbbVie

Leads biologics manufacturing operations across cell culture, purification, filling, and central services. Supervises shift personnel, manages schedules and performance, ensures safety and cGMP compliance, troubleshoots manufacturing issues, supports investigations and CAPAs, maintains audit readiness, oversees batch records and SOPs, and develops manufacturing staff. Requires biotechnology or pharmaceutical manufacturing expertise, supervisory experience, and knowledge of quality systems and complex biopharmaceutical processes.

Supports QC microbiology operations for routine testing and new product introductions involving small-molecule and biologic products. Responsibilities include GMP and EHS compliance, laboratory documentation, investigations, audits, infrastructure and instrumentation readiness, equipment qualification, calibration support, trend tracking, and continuous improvement. Collaborates cross-functionally to resolve issues, maintain operational readiness, and support timely product launches.

Performs cGMP biologics manufacturing operations across upstream, downstream, or central service streams. Executes validated processes, completes batch documentation, troubleshoots deviations, supports quality and safety compliance, leads shift operations, assigns work, trains biotechnologists, and acts as deputy manufacturing supervisor. Responsibilities include audit readiness, quality records, process improvements, production planning, and resolution of anomalous processing events.

Leads Medical Affairs for Allergan Aesthetics across Singapore, distribution markets, and Asia launches. Responsibilities include KOL engagement, scientific exchange with healthcare professionals, medical education, launch preparation, advisory boards, Phase IV and investigator-initiated studies, pharmacovigilance support, compliance, strategic planning, and cross-functional collaboration. The role requires approximately 60% travel and serves as a regional medical resource for internal and external stakeholders.

Manages hematology key accounts and hospital relationships to drive product sales and market penetration. Develops strategic partnerships with healthcare stakeholders, including KOLs and therapy experts; analyzes sales and market data; forecasts demand; identifies business opportunities; coordinates promotional programs; manages formulary listings, tenders, budgets, and internal approvals; and executes account strategies through frequent field engagement and cross-functional collaboration.

Supports pharmaceutical Quality Operations across manufacturing, warehouse, engineering, and QC. Reviews batch records and inspection documentation, assists with material and product release, investigates non-conformances, supports CAPA and change control, trends quality data, assesses risks, and contributes to product reviews, quality systems, new product introductions, and continuous-improvement initiatives during a 15-month training program.

Performs biologics manufacturing operations in a cGMP production facility, including method transfer, equipment setup and calibration, quality testing, process adjustments, documentation, data analysis, and campaign support. Coordinates work across sub-groups, tracks issues, develops solutions to moderate-complexity problems, and ensures compliant execution of production procedures. Requires knowledge of media and buffer preparation, cell culture or biological drug purification, safety and quality systems, cGMP, and technology transfer.

Performs cGMP biologics manufacturing operations across upstream, downstream, and central services, including cell culture, purification, buffer and media preparation, autoclaving, glasswashing, and filling. Completes batch documentation, operates DeltaV, SAP, and MES systems, troubleshoots equipment and process issues, supports production scheduling, participates in investigations, and coaches junior biotechnologists. The role requires cleanroom work and rotating shifts.

Supports quality training and document control in a regulated biomedical manufacturing environment. Responsibilities include maintaining LMS training records, coordinating courses, managing GMP documentation changes, issuing controlled records, reconciling and archiving GxP documents, publishing training metrics, and supporting data integrity and continuous-improvement initiatives.

Participate in a 15-month training program supporting API manufacturing operations. Execute batch instructions and processing steps, operate DeltaV and POMS/MES systems, complete GMP/GDP documentation, resolve batch errors, support safety assessments, and contribute to digitalization and continuous improvement. The role requires working 12-hour rotating day and night shifts while maintaining quality, compliance, safety, and production schedules.

Participate in a 15-month training program supporting biologics manufacturing. Provide technical support, troubleshoot processes, analyze manufacturing data, execute process improvements, support technology transfers, and contribute to continuous improvement. Prepare technical documentation, including batch records, SOPs, investigations, protocols, risk assessments, and technical reports, while developing foundational biomanufacturing expertise under supervision.

Participate in a 15-month biomanufacturing training program supporting cGMP production of biologics drug substance. Perform upstream, downstream, or central-services activities; operate and clean equipment; complete batch documentation; maintain inventory and plant readiness; troubleshoot processing issues; report anomalies; and contribute to continuous improvement. The role develops hands-on expertise in biologics manufacturing, quality compliance, safety, and manufacturing systems.

Participate in a 15-month training program supporting preventive, predictive, and corrective maintenance for manufacturing equipment and utility systems. Assist with troubleshooting, breakdown investigations, CMMS work orders, shutdowns, inspections, reliability initiatives, root cause analysis, CAPA, change controls, data analysis, and continuous improvement projects while developing practical engineering and maintenance skills.

Lead Singapore statutory accounting, financial statement preparation, audit coordination, compliance filings, tax support, reconciliations, and internal controls. Coordinate statutory reporting and audit activities across JAPAC entities while partnering with affiliates, auditors, tax advisors, shared services, and BPO providers. Drive standardization, documentation, automation, risk escalation, remediation, and continuous improvement across regional statutory processes.

Lead supplier relationships and oversee external manufacturing for designated products, ensuring quality, regulatory compliance, on-time delivery, cost control, and program management across cross-functional teams.