Jobs at AbbVie

Manages pharmaceutical regulatory submissions and product registrations, including new products, variations, labeling updates, deficiency responses, and marketing approval maintenance. Coordinates with regulatory authorities and internal stakeholders, monitors regulatory changes, evaluates business impacts, maintains regulatory SOPs, and supports process improvements. Requires expertise in Taiwan regulatory requirements for new chemical entity applications and a degree in pharmacy, pharmacology, biology, or a related field.

Performs advanced maintenance support for department assets, ensuring equipment reliability, quality, safety, and GMP compliance. Conducts root cause investigations, reliability-centered maintenance analysis, advanced troubleshooting, and continuous improvement activities. Trains lower-level technicians, applies multiple skilled trades, supports cross-functional teams, and maintains equipment using electrical, diagnostic, machine, and predictive tools.

Maintains and enhances enterprise purchasing systems and related data, analyzes business needs, develops requirements and specifications, coordinates system changes and testing, maintains documentation, supports training, and monitors system performance, controls, accessibility, and compliance. The role collaborates with business and technical teams, produces reports and ad hoc database analyses, supports application administration, and helps plan system resources and delivery timelines.

Leads global commercial balance sheet planning, forecasting, consolidation, and actuals reporting across financial cycles. Oversees capital budget consolidation, intangible asset impairment assessments, DSO/DPO/WAPT reporting, audits, SOX controls, process improvements, and financial analytics. Partners cross-functionally to communicate risks and recommendations while coaching two finance professionals.

Leads purchase-based contracting finance across pharmaceutical products and channels. Manages pricing and discount contract portfolios, supports compliant implementation, advises analysts, partners cross-functionally, improves processes and systems, leads special projects, and supports SOX and audit activities. Requires strong financial analysis, communication, organizational, and stakeholder-management skills, plus expertise in Model N and advanced Excel.

Leads Commercial Finance transformation initiatives across processes, tools, business partnership, and people experience. Drives project execution, finance systems and data governance strategy, change management, communications, culture programs, capital planning, crisis management support, and SharePoint development. Partners with Corporate Finance, supports the Vice President, and manages a team delivering technology and process simplification solutions.

Leads scientific investigations, process development, scale-up, technology transfer, process validation, troubleshooting, and continuous improvement for late-stage and commercial antibody and ADC manufacturing. Supports new product introduction, CMC lifecycle management, product investigations, regulatory submissions, agency inspections, and manufacturing at internal or third-party sites. Collaborates cross-functionally with process development, manufacturing, quality, and regulatory teams while applying scientific, engineering, and statistical principles.

Provides legal counsel on complex mergers, acquisitions, pharmaceutical licensing, collaborations, joint ventures, and strategic alliances. Drafts and negotiates transaction agreements, conducts due diligence, advises on antitrust and competition risks, manages outside counsel, interprets complex contracts, and supports senior management on significant corporate matters.

Advise AbbVie’s business development and acquisitions teams on complex pharmaceutical M&A, licensing, collaborations, joint ventures, and strategic alliances. Draft and negotiate transaction agreements, conduct due diligence, assess antitrust risks, interpret contracts, manage outside counsel, and provide strategic legal guidance to management and cross-functional stakeholders. Supervise legal support staff and ensure compliance with corporate policies and applicable laws.

Leads US regulatory affairs strategy for oncology advertising and promotion. Oversees cross-functional therapeutic teams, regulatory compliance, processes, budgets, productivity, strategic initiatives, and senior-management presentations. Partners with Medical, Marketing, Legal, Regulatory, and Public Affairs teams while managing departmental operations, mentoring staff, and evaluating business trends and risks.

Leads US and Canada regulatory strategy for pharmaceutical products, including FDA interactions, regulatory submissions, approval processes, registration maintenance, and responses to health authorities. Partners with cross-functional teams, advises on regulatory issues, negotiates project decisions, interprets regulations, and supports product commercialization in a complex matrix environment.

Leads US and Canadian regulatory strategy for pharmaceutical products across development and commercialization. Responsibilities include FDA and Health Authority engagement, regulatory submission preparation and review, responses to inquiries, registration maintenance, cross-functional advisory support, and implementation of regulatory strategies. The role requires independent decision-making, negotiation, consensus building, and collaboration across regulatory, clinical, legal, commercial, and public affairs teams.

Leads intercontinental oncology medical affairs strategy and operations for hema-oncology products. Provides scientific input to brand, clinical development, research, regulatory, and market access strategies; supports clinical trials and investigator-initiated studies; trains affiliates and cross-functional teams; engages external experts and professional societies; and contributes to regulatory discussions and scientific communications.

Leads US regulatory advertising and promotion strategy for oncology, directing cross-functional teams and multidivisional initiatives. Oversees regulatory compliance, processes, policies, budgets, productivity, staffing, and departmental operations. Partners with Medical, Marketing, Legal, Regulatory, and Public Affairs stakeholders; evaluates business trends, develops strategic recommendations, manages complex projects, presents to senior leadership, and mentors staff.

Leads US regulatory advertising and promotion strategy for oncology, overseeing cross-functional teams, initiatives, processes, budgets, productivity, and compliance. Partners with Medical, Marketing, Regulatory, Legal, and Public Affairs stakeholders; evaluates business trends and risks; develops policies and recommendations; presents to senior leadership; and manages or mentors staff. The hybrid role requires substantial pharmaceutical regulatory experience and direct responsibility for advertising and promotion regulations.

Field-based pharmaceutical sales representative responsible for executing dermatology brand strategy, managing a territory, meeting sales and marketing targets, developing healthcare-provider relationships, delivering product presentations, addressing objections, gathering market intelligence, and engaging disease-state experts and speakers. Requires scientific and therapeutic expertise, strong selling and presentation skills, healthcare credentialing, a valid driver’s license, and safe driving eligibility.

Develops and implements US and Canada regulatory strategies for pharmaceutical products across development and commercialization. Coordinates FDA interactions, briefing packages, regulatory submissions, responses to health authorities, and registration maintenance. Advises cross-functional stakeholders, negotiates project matters, interprets regulations, supports approval processes, and contributes to staff training in a complex matrix environment.

Provides advanced executive and operational support to a Vice President and leadership team. Responsibilities include complex calendar and correspondence management, domestic and international travel coordination, expense processing, large-scale event planning, SharePoint administration, confidential records management, onboarding support, purchase orders, invoice processing, procurement, vendor coordination, and cross-functional communication.

Leads US regulatory advertising and promotion strategy for oncology products, directing cross-functional teams and complex initiatives. Oversees regulatory compliance, process improvement, productivity, budgets, communications, and strategic presentations. Partners with Medical, Marketing, Legal, Regulatory, and Public Affairs teams while mentoring staff and managing departmental operations in a hybrid headquarters environment.

Leads a global team responsible for clinical process design, change management, continuous improvement, and quality system integration within pharmaceutical R&D. Oversees strategic programs, clinical research process infrastructure, system enablement, quality document architecture, performance assessment, workload prioritization, and stakeholder alignment. Provides team leadership, coaching, performance management, and career development while ensuring compliance with GCP, SOPs, ICH guidelines, global regulations, ethics, and compliance standards.