AbbVie

AbbVie

Global biopharmaceutical company developing medicines

Principal Salesforce Engineer - Salesforce

Full-Time
$124.5k - $236.5k/yr

+ Long-term incentive program

Senior, Expert
Bachelor's, Master's, PhD
North Chicago, IL, USA
Hybrid

About the job

Requirements
  • A Bachelor's degree or equivalent education with 8 years of experience, a Master's degree or equivalent education with 7 years of experience, or a PhD with 3 years of experience in application strategy, requirements, architecture, design, engineering, and related technology disciplines.
  • Experience planning, architecting, designing, developing, integrating, and operating CRM solutions on the Salesforce platform using Service Cloud, Experience Cloud, and Health Cloud or Life Sciences Cloud.
  • Deep hands-on experience with Salesforce CRM technical capabilities, including workflow automation, responsive user interfaces, data architecture, relational data modeling, data migration, data quality management, application programming interface engineering, integration design, and platform configuration.
  • In-depth knowledge of the systems development life cycle, enterprise application development practices, and technology alternatives for complex business systems.
  • Demonstrated experience leading large enterprise projects with responsibility for business requirements analysis, solution architecture, technical design, and end-to-end solution delivery.
  • Demonstrated ability to lead technically complex initiatives, influence stakeholders, and provide guidance to engineering teams, architects, and vendor partners.
  • Strong understanding of enterprise architecture principles, Salesforce Well-Architected concepts, and the design of scalable, sustainable, and supportable enterprise solutions.
  • Hands-on experience with Salesforce development and configuration tools, including Apex, Triggers, Lightning Web Components, Flows, and integration features.
  • Strong background in integration architecture and engineering, including REST and SOAP APIs, middleware-based integrations, direct system-to-system interfaces, and enterprise integration patterns.
  • Demonstrated ability to apply object-oriented design principles and design patterns to enterprise solutions.
  • Experience with DevOps, CI/CD/CT practices, and Salesforce ecosystem delivery tooling to support automated, repeatable, and high-quality releases.
  • Excellent verbal and written communication skills, with the ability to present complex technical concepts clearly to senior BTS leaders, business stakeholders, and cross-functional partners.
Responsibilities
  • Own the system architecture and engineering standards within the OnePRM platform and ensure alignment with Salesforce Platform architecture principles, solution architecture standards, Salesforce best practices, security requirements, validated systems expectations, and SLC governance.
  • Serve as the principal architecture and engineering leader for OnePRM by shaping solution direction, technical architecture and design, data modeling, integration strategy, engineering decisions, and platform evolution.
  • Drive the OnePRM technical strategy and multi-year roadmap for systems, including modernization, migration, consolidation, and future-state platform design.
  • Evaluate emerging Salesforce capabilities, AI-enabled solutions, and engineering tools; lead proofs of concept; and translate successful pilots into scalable, production-ready capabilities.
  • Lead multiple engineering PODs and blended teams across architecture, development, quality assurance automation, DevOps, and vendor partners, ensuring accountability for delivery commitments, quality standards, and engineering outcomes.
  • Define and govern scalable data models, workflow automation, secure integration patterns, and resilient enterprise interfaces across Salesforce and connected platforms.
  • Partner with program, product, and business leaders to execute complex release plans, manage dependencies, mitigate technical risks, and coordinate concurrent workstreams.
  • Drive CI/CD/CT modernization and shift-left quality practices, including automation, code analysis, testing rigor, and compliance controls.
  • Establish and govern design review, code review, release readiness, and pre-deployment approval processes across internal and external delivery teams.
  • Govern technical debt, refactoring, and remediation as strategic investments to strengthen maintainability, reduce risk, and improve platform scalability.
  • Maintain standards for data quality, documentation, privacy, security, and compliance in accordance with AbbVie policies, validated system requirements, and enterprise governance expectations.
  • Coach and develop application architects, technical leads, and senior engineers; strengthen technical depth across the team; and build succession capability for critical architecture and engineering roles.
  • Partner with senior business leaders, product owners, architects, and external partners to translate strategic needs into sustainable solutions and prioritize investments.
  • Oversee team capacity, vendor performance, and budget utilization to optimize delivery efficiency, maintain accountability, and steward engineering investments.
Desired Qualifications
  • Pharmaceutical or life sciences industry experience.
  • Experience with Salesforce Data 360 and Agentforce.
  • Experience with agentic software engineering using Agentforce Vibes.
  • Salesforce Administrator, Platform App Builder, Platform Developer I, Application Architect, or System Architect certification, or active pursuit of architect-level credentials.
  • Additional Salesforce Consultant certifications, such as Sales Cloud, Service Cloud, or other relevant cloud certifications.
  • Salesforce certifications in Data Architecture and Management and Integration Architecture.

About the company

AbbVie is a global biopharmaceutical company that develops and sells medicines to treat serious health conditions. Its portfolio spans immunology, oncology, virology, neuroscience, and aesthetics, with products designed to modulate the immune system, target disease pathways, or support medical aesthetics. AbbVie compounds its products through a heavy emphasis on research and development, investing billions to build a steady pipeline of new therapies. Its medicines are brought to market by selling to healthcare providers, hospitals, and clinics, and in some cases directly to patients via prescriptions. The company differentiates itself through a wide, globally distributed product line, substantial R&D investment, and a commitment to sustainability and patient care, including science-based targets. AbbVie’s goal is to improve patient outcomes by delivering effective treatments for unmet medical needs while pursuing long-term, responsible growth across healthcare markets.

Company Size

10,001+

Company Stage

IPO

Headquarters

North Chicago, Illinois

Founded

1888

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Simplify's Take

What believers are saying

  • RINVOQ gained European approval for juvenile idiopathic arthritis on September 22, 2026.
  • July 2026 European approval expanded RINVOQ in severe alopecia areata.
  • Etentamig delivered 74% response rates in September 2026 myeloma data.

What critics are saying

  • Humira sales fell 36.1% in July 2026, exposing lingering erosion.
  • Apogee dilutes 2026 EPS by $0.14, then $0.46 in 2027.
  • Rinvoq and Skyrizi face 2033 patent pressure despite current settlements.

What makes AbbVie unique

  • Skyrizi and Rinvoq anchor AbbVie’s post-Humira immunology franchise in 2026.
  • Apogee acquisition adds zumilokibart and asthma biology after September 3, 2026.
  • Iambic collaboration broadens AI discovery across immunology, neuroscience, and oncology.

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Benefits

Remote Work Options

Flexible Work Hours

Professional Development Budget

Growth & Insights and Company News

Headcount

6 month growth

5%

1 year growth

5%

2 year growth

5%
finanzen.at
Sep 21st, 2026
ADARx Pharmaceuticals prices IPO of 21.9M shares at $15-17, expects to raise $397M

ADARx Pharmaceuticals has priced its initial public offering of 21.875 million shares between $15.00 and $17.00 per share, according to an SEC filing. The San Diego-based late-clinical stage biotechnology company has applied to list on Nasdaq under the ticker "ADRX". AbbVie has agreed to purchase shares in a concurrent private placement that would give it approximately 4.9% ownership of ADARx's outstanding stock. Underwriters have a 30-day option to purchase up to 3.28 million additional shares. The company estimates net proceeds of approximately $397.1 million, or $445.9 million if underwriters exercise their option in full, assuming a $16.00 share price. Proceeds will fund clinical trial development and general corporate purposes.

PR Newswire
Sep 21st, 2026
AbbVie partners with Iambic to accelerate AI-driven drug discovery in immunology, neuroscience and oncology

AbbVie and Iambic Therapeutics have entered into a multi-year collaboration to accelerate AI-driven drug discovery in immunology, neuroscience, and oncology. The partnership will combine Iambic's molecular superintelligence platform with AbbVie's therapeutic expertise to develop small molecule therapies with first-in-class and best-in-class potential. The collaboration will utilise Enchant v3, Iambic's next-generation multimodal transformer model trained on over 6,000 molecular properties. This technology is designed to optimise candidate properties simultaneously, reducing drug discovery timelines whilst improving success rates. Under the agreement, Iambic will receive an upfront payment and is eligible for success-based milestone payments and tiered royalties on net sales from products generated through the collaboration. The partnership aims to accelerate the discovery process and deliver breakthrough medicines to patients more quickly.

AbbVie
Sep 20th, 2026
AbbVie Completes Acquisition of Capstan Therapeutics

Acquisition adds a potential first-in-class in vivo targeted lipid nanoparticle (tLNP) anti-CD19 CAR-T therapy candidate for B cell-mediated autoimmune diseases as well as a proprietary tLNP...

AbbVie
Sep 19th, 2026
AbbVie Completes Acquisition of Apogee Therapeutics

Acquisition deepens AbbVie's robust immunology pipeline with diverse assets targeting dermatologic, respiratory and other inflammatory and immunological diseases Apogee's lead asset, zumilokibart,...

AbbVie
Sep 18th, 2026
AbbVie Highlights New Real-World Data Supporting the Effectiveness of VRAYLAR(R)(cariprazine) at Psych Congress 2026

September 18, 2026 AbbVie highlights new real-world data supporting the effectiveness of VRAYLAR(R)(cariprazine) at Psych Congress 2026. * New data from prospective real-world studies of VRAYLAR showed meaningful improvements in depressive symptoms, functioning and quality of life among adults living with major depressive disorder (MDD) and bipolar I (BP-I) depression * These findings provide additional evidence that the benefits observed with VRAYLAR in clinical trials can also be achieved in routine practice, where patients often have more complex treatment needs NORTH CHICAGO, Ill., Sept. 18, 2026 /PRNewswire/ - AbbVie (NYSE: ABBV) today presented new VRAYLAR(R)(cariprazine) data at Psych Congress 2026 in New Orleans, including results from two prospective real-world observational studies in major depressive disorder (MDD) and bipolar I disorder (BP-I). The findings reinforce that the efficacy established in clinical trials translates to effectiveness in the broader, more clinically complex patient populations healthcare providers treat every day. "Because mood disorders are highly heterogeneous, it is critical to evaluate treatments in real-world settings where care is delivered every day," said Mudra Kapoor, M.D., vice president, global medical affairs, AbbVie. "These prospective studies provide additional evidence that VRAYLAR can help patients achieve meaningful improvements in depressive symptoms, functioning and other patient-centered outcomes in routine clinical practice." In the real-world BP-I depression study, CReW BP-I, patients treated with VRAYLAR experienced significant improvements in depressive symptoms as well as outcomes that affect daily life, including functioning and quality of life, after 12 weeks of treatment in routine clinical practice; the most common adverse events were nausea and dizziness. In ProACt, a real-world study of adjunctive VRAYLAR in MDD, interim findings showed improvements not only in depressive symptoms, but also in outcomes that affect day-to-day life and matter most to patients, including functioning, motivation, energy and anhedonia. In addition to these real-world studies, AbbVie also presented an indirect comparative analysis in MDD, long-term pediatric safety data, and patient preference research evaluating treatment approaches following inadequate antidepressant response. "For clinicians, one of the most important questions is whether the benefits demonstrated in clinical trials hold up in the real world, where patients have unique needs, experiences and treatment journeys," said Andrew J. Cutler, M.D., an author of the ProACt study, Clinical Professor of Psychiatry at SUNY Upstate Medical University and Chief Medical Officer of the Neuroscience Education Institute. "These studies reinforce what has been established in VRAYLAR clinical trials and provide additional confidence that meaningful improvements in symptoms, functioning and patient-reported outcomes can be achieved beyond the controlled environment of a trial. That kind of real-world validation is valuable when making individualized treatment decisions in everyday clinical practice." MDD and BP-I can profoundly affect every aspect of a person's life and often require long-term, comprehensive care. Approximately one in five U.S. adults will experience MDD during their lifetime, and nearly 11 million adults are living with bipolar disorder, yet many continue to experience ongoing symptoms despite available treatments - highlighting persistent unmet treatment needs.