Jobs at AbbVie

Performs chemical and physical testing of pharmaceutical materials and products, verifies laboratory records, manages samples and data packs, investigates out-of-specification results, and ensures compliance with cGMP, FDA, GLP, QSR, and SOP requirements. Coaches QC analysts, supports scheduling and productivity, authors validation and compliance documents, troubleshoots analytical issues, and drives laboratory continuous improvement and safety initiatives.

Provides confidential executive support to the General Manager and leadership team, including calendar, meeting, travel, correspondence, events, records, and expense management. Supports HR administration, leave systems, onboarding, vendors, and purchase orders. Oversees office, facilities, catering, budgets, suppliers, and workplace services. Serves as site EHS representative, coordinating safety training, assessments, emergency preparedness, fire safety, and compliance documentation.

Leads aseptic product quality assurance across AbbVie’s external manufacturing network. Responsibilities include assessing third-party manufacturers, conducting due diligence, overseeing aseptic investigations, evaluating contamination-control practices, ensuring regulatory compliance, mitigating manufacturing risks, monitoring industry and regulatory developments, and driving continuous improvement. The role provides strategic and technical quality leadership while collaborating with internal sites, contract manufacturers, and cross-functional stakeholders to resolve significant quality issues and protect product quality and supply continuity.

Designs, configures, integrates, tests, and optimizes MES solutions across AbbVie’s global pharmaceutical manufacturing network. Leads technical standards, templates, documentation, governance, training, and Communities of Practice while supporting digital transformation and process improvement. Collaborates with manufacturing, automation, IT, and external partners; ensures cGMP and regulatory compliance; and mentors MES engineers and other contributors.

Supervise warehouse operators and coordinate receiving, storage, sampling, dispensing, inventory control, cycle counting, and shipping activities. Ensure accurate SAP transactions, FIFO material issuance, documentation, GMP compliance, safety, training, and inspection readiness. Monitor performance, resolve or escalate deviations, collaborate with cross-functional teams, and drive continuous improvement. Manage team capability through coaching, appraisals, development planning, and performance counseling.

Lead operations brand/program activities to align product strategy with business goals. Manage supply chain interfaces, forecasts, lifecycle transitions, contract negotiations with TPMs, risk mitigation, and cross-functional stakeholder coordination to ensure assurance of supply and cost savings.

Support global packaging PMO by coordinating project execution, running PMO processes and meetings, administering the Cora capital project system, preparing capital expenditure justifications and savings analyses, tracking project status, and planning/executing process improvements and smaller capital projects.

Supervise QC laboratory operations, lead and develop QC chemists, ensure cGMP and regulatory compliance, support production schedules, manage samples and equipment, maintain data integrity and documentation, deliver training, and drive continuous improvement and method support.

Lead and develop a global labeling operations team responsible for labeling strategy, packaging artwork, launch project coordination, forecasting, and cross-functional collaboration. Drive continuous improvement, manage resources and day-to-day labeling activities, report metrics, and ensure artwork availability for regulatory submissions and production while influencing senior stakeholders and implementing change management.

Lead the site PMO to establish governance, manage the project portfolio (NPI, CAPEX, strategic initiatives), allocate resources, mitigate risks, and report to senior plant leadership. Standardize methodologies for compliance, drive cross-functional collaboration, and support continuous improvement and business excellence.

Lead and supervise production operators to meet daily and weekly production and quality targets in a cGMP pharmaceutical manufacturing environment. Ensure adherence to SOPs and BMRs, coach and develop staff, run Tier meetings, manage deviations with QA, maintain documentation, drive continuous improvement and enforce safety and housekeeping standards.

Lead design, assessment, and implementation of OT/ICS security solutions for manufacturing and research environments. Perform secure-by-design reviews, risk and vulnerability assessments, incident response support, and recommend mitigations. Collaborate with operations, engineering, and vendors to harden OT networks, map data flows, and deploy controls using industry standards to improve resilience and compliance.

Provide functional and technical SAP support for global supply chain, designing and configuring SAP MM/WM/EWM solutions, leading blueprint workshops, supporting integrations and CSV activities, managing stakeholders, mitigating implementation risks, and enabling continuous process improvements.