12+ weeks parental leave + Verified parental leave values jobs

Senior Java Engineer - Distributed Systems - Elasticsearch North America, United States Elastic, the Search AI Company, enables everyone to find the answers they need in real time, using all their data, at scale - unleashing the potential of businesses and people. The Elastic Search AI Platform, used by more than 50% of the Fortune 500, brings together the precision of search and the intelligence of AI to enable everyone to accelerate the results that matter. By taking advantage of all structured and unstructured data - securing and protecting private information more effectively - Elastic's complete, cloud-based solutions for search, security, and observability help organizations deliver on the promise of AI. What is The Role: We are on the lookout for a Senior Software Engineer to join our Elasticsearch - Distributed Systems team and focus on how Elasticsearch provides scale, performance, and resilience. This team owns how nodes in an Elasticsearch cluster communicate, and how data are indexed, allocated, and replicated across nodes. What You Will Be Doing: - Improving Elasticsearch's components that support concurrent and consistent indexing across multiple machines. - Maintaining our cluster coordination system to keep performance high even though nodes come and go from the cluster and data moves around, while maintaining the safety and liveness properties of the system as a whole. - Pushing the limits on the number of shards, nodes, and petabytes that Elasticsearch can handle today - Looking into all kinds of issues, including performance or concurrency issues, and proposing solutions. -

Manager, Access and Reimbursement Services North Chicago, IL, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: Purpose The Access and Reimbursement Support Services Manager will effectively manage the support center in order to provide the highest level of service to patients, health care providers (HCP), and internal and external customers, ensuring that inbound and outbound calls and corresponding inquiries and issues are completed all in alignment with key performance indicators. This role will also drive continuous improvement initiatives for activities and products provided. Responsibilities: Lead a team of supervisors who manage operations to deliver superior customer service, driving world-class leadership and strong performance. Monitor department and employee productivity levels, identify opportunities to improve optimization and enable implementations and cost controls. Monitor internal programs, similar industry programs and regulatory guidance to ensure program relevance and compliance. Lead and mentor direct reports responsible for operations of designated AbbVie products. Provide recommendations regarding appropriate promotional and business practices. Develop and manage relationships with payors, providers, and customers. Partner with commercial business partners

Medical Science Liaison, Hematology Oncology, Quebec Atlantic Remote | Montreal, QC, Canada Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Recruitment Fraud Alert AbbVie has become aware of fraudulent recruitment-related phishing attempts. We encourage all candidates to remain vigilant and exercise caution when responding to messages regarding employment opportunities. AbbVie in Canada recruiters will only communicate with candidates using an official @abbvie.com email address or a verified LinkedIn account. Joining AbbVie means you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients' lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada. When choosing your career path, choose to be remarkable. AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, vision care, virology, women's health , and gastroenterology, in addition to products and services

Director, RA Global Regulatory Strategy North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Director Regulatory Affairs Global Regulatory Lead (GRL II) Global Regulatory Strategy, is responsible for developing and implementing global strategies to secure and maintain market approval for product(s) in the assigned therapeutic area. Leads the Global Regulatory Product Team (GRPT). Continually expands TA knowledge, and ensures strategic messaging and content of global regulatory dossiers. May lead the Labeling Regulatory Strategy Team (LRST). Serves as the primary regulatory interface with AST and supporting teams. Proactively anticipates and mitigates regulatory risks. Ensures compliance with global regulatory requirements. Manages compounds through all phases of development, including post approval and throughout the life cycle of the product. Demonstrates excellent understanding of drug development and leadership behaviors consistent with level. Develops and implements acceleration strategies. Manages projects and necessary documentation of reg strategies. Responsibilities Interfaces with the LRST and AST to lead and support cross-functional company objectives. Leads the GRPT to development of creative global strategies in line with applicable regulations to achieve

Associate Director, International Market Analytics and Business Intelligence, Migraine Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Associate Director , International Market Analytics and Business Intelligence (IMABI) plays an essential role in driving insights for the Migraine prevention franchise and ensuring continued successful launches and uptake for Aquipta in our OUS markets. The AD will ensure market and stakeholder insights drive informed strategic and operational decisions for the brands. She/He will lead Business Intelligence and Analytics activities (primary market research, launch KPIs and market & brand performance tracking, and competitive intelligence) and be responsible for generating new and credible insights to support actionable recommendations that address key business needs and objectives. The Associate Director will manage all aspects of Business Intelligence, including project planning, initiation of the RFP process, Vendor Selection, Study Design, Contract Execution and Budget Management Key Responsibilities Include : Serve as the IMABI lead for the Migraine prevention assets. Responsible for partnering strategically with International, Area and Affiliate leadership, guiding brand and co positioning strategies. Drive using an

Principal Research Scientist II Engineering - Material Sciences North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Research and Development Process Engineering team is responsible for developing processes that enable delivery of AbbVie's candidate molecules in a dosage form which is intended for product commercialization. We have an exciting opportunity for a Material Science and Engineering Leader based in North Chicago, IL. The R&D Process Engineering group is responsible for enabling drug development by devising fit for purpose manufacturing processes to provide high quality drug substances and drug products for both development studies and clinical supply materials. We are seeking a Material Science and Engineering Leader for solid oral drug product development projects. Individuals should be experienced with drug product process unit operations and material characterization equipment. Key Responsibilities: Lead Material Science and Engineering Forum - Direct team to focus on project success, innovation and scientific branding Solid Oral Project Assessments - Assess and provide recommendations for all early phase solid oral formulations and manufacturing platforms to ensure resulting materials are

Senior Product Manager Shanghai, Shanghai, China Company Description: About AbbVie At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit https://global.allerganaesthetics.com/. Follow Allergan Aesthetics on LinkedIn. Job Description: Develop, optimize and implement the Annual Marketing Plan of Botox in Tx. Engage KOL to ensure strong brand endorsement from KOLs. Monitor market trends, competitive environment and customer insight as well as brand performance to evaluate the effectiveness of marketing activities. Work closely with cross-functional team as well as Botox cosmetic to synergize marketing resource. Ensure the integrity of Botox therapeutic marketing activities in accordance with local, regional and corporate compliance policies Effectively development and manage promotional budget to deliver annual marketing plan Lead open, consistent and clear communication between sales and marketing Update sales force training material and implement the new employee orientation training. Qualifications: Education and Experience Bachelor degree or above in medical or related medicine science 4+ years Pharmaceutical marketing experience (related consulting background is a plus) Experience in marketing consumer-oriented products (pharmaceutical or cross-industry) is a preferred qualification. Essential Skills, Experience, and Competencies (includes Licenses, Credentials) Strong teamwork spirit with the ability to collaborate effectively across cross-functional and cross-departmental teams. Good written and verbal communication skills, with the ability

Principal Engineer, Quality - Automation and AI North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Principal Quality Engineer - Automation and AI Enablement is responsible for ensuring that AbbVie's IT operations and software lifecycle processes fully comply with regulatory requirements and corporate standards. This role provides leadership in defining, implementing, and optimizing quality systems through digital enablement and AI-driven solutions, collaborating directly with cross-functional teams. Focusing on modernizing communications, metrics management, SLC monitoring activities, and providing end-to-end audit and Corrective and Preventive Action (CAPA) support, the incumbent leverages automation and AI to strengthen cross-functional integration and quality oversight. They drive improvement initiatives, support audit readiness, ensure effective issue tracking and resolution, deliver actionable insights through metrics and reporting, and act as the primary point of contact between business units and quality teams to maintain mutual understanding and effective service agreements. Key Responsibilities: Develop, implement, and champion solution/change strategies to align with organizational objectives and evolving regulatory requirements, leveraging AI-powered solutions and automation to enhance compliance monitoring and operational efficiency. Apply

Technician, Pharmaceutical Sligo, SO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are recruiting a Pharmaceutical Technician to join our team on site in Manorhamilton Road, Sligo on a 12 month fixed-term contract. This role is rotational shift work. In your role as Pharmaceutical Technician you will be responsible for producing drug product materials as per organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements. A snapshot of your key responsibilities as a Pharmaceutical Technician would be: Pharmaceutical processing activities in our manufacturing building and support locations. Team co-ordination to maximise the effectiveness of the team members. Documentation of all activities in line with cGMP requirements. Cross training within the team and training of new team members. Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems. Execution of commissioning and validation protocols on an ongoing basis. Maintaining the overall cGMP of the pharmaceutical processing areas. Adheres

Senior Counsel, Global Commercial Legal - U.S. Market Access and Pricing North Chicago, IL, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: The Senior Counsel, Global Commercial Legal - U.S. Market Access and Pricing is responsible for developing legal strategy and support for the Market Access organization, with a substantial focus on government price reporting. The Senior Counsel will report to the Associate General Counsel, Global Commercial Legal - U.S. Market Access and Pricing. This position will provide counsel on a broad range of legal, compliance, and regulatory issues, with a primary focus on federal price reporting, as well as the Anti-Kickback Statute and the False Claims Act. Responsibilities Serve as counsel for our Government Price Reporting function concerning legal, regulatory, and compliance issues associated with federal government price reporting requirements. Serve as counsel for our U.S. Market Access and Pricing functions advising on price reporting, Anti-Kickback Statute and False Claims Act matters. Provide strategic legal counsel to senior management on product pricing and access matters. Prepare, review, and

Talent Acquisition Coordinator Lead, R&D North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose The Talent Acquisition Coordinator Lead, R&D, plays a critical role in delivering exceptional recruiting operations while leading a team of Talent Acquisition Coordinators. This role combines hands-on execution with leadership responsibility to enhance the end-to-end candidate and hiring manager experience. The incumbent will drive operational excellence and lead initiatives that leverage AI, automation, and innovative technologies to improve efficiency and elevate stakeholder experiences. Responsibilities Lead and develop a team of up to 8 Talent Acquisition Coordinators, setting clear priorities, performance expectations, and development plans Drive adoption and utilization of AI-driven and technology-enabled solutions to enhance recruiting operations and scheduling efficiency Oversee domestic, international, and executive interview coordination, ensuring a seamless and high-quality experience Partner with recruiters and hiring managers to support requisition execution and candidate progression Serve as a subject matter expert for executive hiring logistics and high-touch candidate care Identify and implement process improvements to streamline workflows and increase operational efficiency Manage stakeholder relationships across recruiters,

Labormitarbeiter in der Early Safety Platform (Toxikologie) (all genders) (Vollzeit, befristet für 24 Monate) Ludwigshafen, RP, Germany Unternehmensbeschreibung: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Stellenbeschreibung: Herzlich willkommen bei Abbvie! Als Teil eines internationalen Unternehmens mit über 48.000 Mitarbeitern weltweit und rund 3.000 Mitarbeitern in Deutschland hast Du die Möglichkeit, eng mit uns zusammenzuarbeiten, um die gesundheitlichen Herausforderungen von morgen zu meistern. Du hast eine Leidenschaft für die Verbesserung der Gesundheitsversorgung auf der ganzen Welt? Du möchtest Dein Fachwissen einsetzen, um die Lebensqualität von Patienten zu verbessern? In einem herausfordernden Arbeitsumfeld, das Dir die Möglichkeit bietet, Deine eigenen Fähigkeiten zu erweitern und zu entwickeln? Dann bist Du bei uns richtig! Stell dein Know-how unter Beweis und werde Teil unseres Teams am Standort Ludwigshafen als Labormitarbeiter in der Early Safety Platform (Toxikologie) (all genders) Wir suchen einen motivierten und teamfähigen Labormitarbeiter (all genders) für die Gruppe der Early Safety Platform (Toxikologie) Konkret bedeutet das: Selbständige Durchführung von toxikologischen non-GLP Studien und PK In-vivo Studien, dies beinhaltet die Handhabung von Tieren, Applikationen, Blutentnahmen sowie die klinische Überwachung und Untersuchungen Durchführung von

Product Specialist / Medical Representative Remote | Warsaw, Masovian Voivodeship, Poland Company Description: At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit https://global.allerganaesthetics.com/ . Follow Allergan Aesthetics on LinkedIn. Job Description: This position title on contract - PRODUCT SPECIALIST. Territorial scope (districts): mazowieckie, warmińsko-mazurskie, podlaskie. Job purpose: The Product Specialist's primary responsibility is to coordinate Allergan's relationships with the customers - physicians and pharmacies in its designated area (i.e. HCPs/injectors, pharmacies). The Product Specialist works strategically to increase the awareness and appropriate use of designated AA products. Works in combination with affiliate sales management to define and implement the most effective approach and is responsible for the sales performance of the designated portfolio. Develops, manages and implements business plans and programs in the assigned geographic region to ensure that not only growth targets are achieved but also to establish long term loyalty and commitment with the customers based on ethical principles. Key responsibilities: 1. Commercial Management Responsible for the sales performance of the designated portfolio by engaging with customers in placing orders, presenting commercial policy and seasonal offers benefits. Achieve the quantitative objectives defined for designated geographic territory. Development of sales strategies aligned with AA overall strategic plan. Leverage portfolio

Professional Medical Specialist Remote | Yinchuan, Ningxia, China 公司描述: 艾伯维 公司介绍： 艾伯维的使命是发现和提供创新药物，解决复杂且棘手的疾病难题和未来的医学挑战。我们不懈努力，凭借在多个关键治疗领域的科研创新为人们的生活带来深远影响，包括免疫学、肿瘤学、神经科学，以及艾尔建美学产品组合中的产品和服务。有关艾伯维的更多信息，请访问网站 https://www.abbvie.com。在领英、Facebook、Instagram、X 和 YouTube 上关注AbbVie。 职位描述: 专业医药专员（免疫 ） 负责公司产品在目标区域内的推广，并达成公司的目标。 负责目标区域内客户的管理，包括建立及更新客户资料，维护客户关系等工作，并合理使用公司资源 完成公司规定的各类报表。 搜集区域内竞争对手的信息。 严格遵守公司的道德行为规范（OEC）政策，有效地执行公司的市场计划。 职位要求: 本科或以上学历，医学、药学或相关专业毕业。 从事两年或以上皮科领域，生物制剂或特药的经验，有外资企业工作背景者优先考虑。 具备出色的销售意识以及较强地判断能力。 良好地沟通和语言表达能力。 热爱销售工作，负有责任心，能承受工作压力。 具有团队合作及吃苦耐劳精神。 其他信息: AbbVie是机会均等的雇主，致力于诚信经营，推动创新，改变生活以及服务我们的社区。机会均等雇主/退伍军人/残疾人士。

Graduate Trainee Budapest, , Hungary Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Launch your career with AbbVie Accelerate - our dynamic two-year rotational program designed for recent Master's graduates. At AbbVie, you'll build your skills through hands-on projects, dedicated mentorship, and collaboration with industry experts in a truly international environment. Our commitment to early career talent means you'll gain meaningful experience, grow your confidence, and be empowered to dream bigger and reach higher. As a Trainee, you'll work with cross-functional teams, contribute to strategic initiatives, and help drive impactful change for patients worldwide. Join AbbVie Accelerate to be a part of a movement dedicated to improving lives and let us be the engine behind your ambition and the springboard for your success. Take the leap and accelerate your career journey with us. Your Key Responsibilities will be: Rotational Assignments: Engage in a series of rotational assignments across various functions, including marketing, market access and sales. Gain exposure to different functions and develop a holistic understanding of the industry and AbbVie. Project Management: Lead and contribute

Werkstudent (all genders) Marketing (Neurotoxins/Migraine) Wiesbaden, HE, Germany Unternehmensbeschreibung: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Stellenbeschreibung: Wir suchen tatkräftige Unterstützung für unser Marketing-Team im Bereich Neurotoxins/Migräne. Du möchtest Erfahrung in der Kommunikation eines multi-nationalen Unternehmens sammeln? Du möchtest Einblicke in strategische Marketing-Themen gewinnen und bei der Umsetzung vielseitiger Maßnahmen für unterschiedliche Zielgruppen unterstützen? Du möchtest wissen, wie kollegiale und erfolgreiche Zusammenarbeit mit anderen Fachbereichen aussehen kann? Dann bewirb' dich jetzt und werde Teil unseres Marketing-Teams. Deine Aufgaben : Unterstütze das Team im täglichen Business und arbeite mit bei der Planung und Umsetzung von Kampagnen und Projekten Erstellung und Bearbeitung von Marketingmaterialien wie Präsentationen, Broschüren und digitalen Inhalten Content-Entwicklung und Content-Management für verschiedene digitale und analoge Kanäle Organisation und Durchführung von Kongressen, Events und Veranstaltungen Qualifikationen: Dein Profil : Du studierst Betriebswirtschaftslehre, Gesundheitswissenschaften oder ähnliche Fachbereiche und bist für ein Bachelor-/Masterstudiengang immatrikuliert Du kannst sehr gut mit den Office-Standardprogrammen umgehen Du hast Spaß dich in neue Aufgabenstellungen einzuarbeiten und bringst eigene Ideen zur Lösung von Aufgaben ein Du bist flexibel, kreativ und verfügst über ausgeprägte Kommunikationsfähigkeiten Idealerweise verfügst du

Director I, Purification Development Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are seeking a highly motivated Director reporting to head of Purification Development team to join the Purification Development group within Biologics Drug Substance Development organization. Our group is responsible for the end-to-end development from first in human process development to late-stage process optimization, process scale up, tech transfer to clinical and commercial sites, and process characterization for all biologics modalities at AbbVie Bioresearch Center in Worcester, MA. We contribute to the development of innovative and novel downstream technologies and create valuable intellectual property through the composition of matter and technologies resulting in cost-effective commercial manufacturing processes. The core deliverable of downstream team is to develop robust manufacturing processes and advance innovative technologies using strong fundamentals. The ideal candidate will have prior biologics purification experience and a passion for hands-on laboratory process development. The candidate is also expected to lead the identification and development of novel approaches and technologies to enhance process development efficiency and commercialization. The candidate must exhibit

Project Manager, Marketing Operations Material Review Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Project Manager, Marketing Operations Material Review facilitates the management of Advertising & Promotional materials as they pertain to the U.S. Commercial MRP (Material Review Process). The Project Manager, Marketing Operations Material Review ensures: Facilitation of cross-functional team (Medical, Regulatory, Commercial, Legal, Compliance, others) review and approval of: Advertising materials Promotional materials Sales Training materials Promotional Labeling materials Management of cross functional team members and advertising agencies Open communication of material status with cross-functional team members and advertising agencies Tactical support and project timeline oversight of materials through MRP Consulting and training support to all team members responsible for uploading and approving materials within the MRP Timely review of all promotional, non-promotional materials through U.S. Commercial, Medical reviewers, Regulatory reviewers, and other key stakeholders Additionally, provides key support for: Solutions and contingency plans to facilitate business success Holds self and team accountable for results Serves as a mentor and coaches others on the MRP Proactively provides consulting; expertise

Medical Director, Hematology Clinical Development North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: Oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities: Manages the design and implementation of one or more clinical development programs in support of an overall Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff. Responsibility may extend from early translational development activities to mature product lifecycle management strategies for internal and/or partnered programs. Has overall responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables. Responsible for assessment

Scientist I, Analytical Development Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Investigate, identify, develop, and optimize new methods and techniques to generate reliable and reproducible data in a timely manner. Read and adapt scientific literature to accomplish assignments and demonstrate broad and versatile technical expertise within discipline. Responsibilities Independently design, develop, and optimize robust analytical methods using separations-base techniques (HPLC, icIEF, CE-SDS) to characterize biopharmaceutical products Implement and innovate new experimental protocols/techniques. Understand the goal and maintain a high proficiency in his/her projects as well as the overall program. Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner. Perform routine and complex tasks competently and independently and generate reliable and consistent results. Troubleshoot complex analytical issues and implement innovative solutions to improve method performance and efficiency. Impact projects mostly through lab and/or pilot plant based activities. Responsible for compliance with all applicable Corporate

Director, HEOR Strategy, Neuroscience Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Leads the development & execution of projects for multiple on-market and/or pipeline development assets potentially across multiple geographies. Is the brand/asset leader representing HEOR on cross functional teams and in the pipeline commercialization teams. Accountable for HEOR strategies and execution, looks to shape brand/asset/enterprise strategies by bringing in expertise and experience within and beyond his/her subject matter expertise. Ensures project plans across all products within their TA portfolio integrates and aligns with the product strategy plans from matrix groups as well as commercial interests and scientific integrity of studies. W/a view across TA assets, ensures there is no overlap of projects and leverages endeavors across the TA; provides updates on execution of plans to products as well as functional management. In the development of product strategic plans, liaises with other members of the product team to generate innovative ideas and get buy-in to strategies Responsibilities List up to 10 main responsibilities for the job. Include information about the accountability

Scientist I, Cell and Molecular Biologist North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Description: AbbVie Oncology Discovery is seeking a highly motivated and experienced cancer cell biologist to support drug discovery projects in our in vitro cancer biology team with a focus on antibody-drug conjugates. The candidate will work closely with a team of experienced scientists to develop and optimize key pharmacological, biochemical and cell-based assays to support multiple programs. Key Responsibilities: Design and execute in vitro studies to assess novel antibody-drug conjugates Analyze and interpret experiments and present data to the broader project team and group meetings. Propose relevant follow-up experiments as needed. Troubleshoot and/or optimize experimental procedures as needed to further the program goals. Contribute to the preparation of data packages for scientific publications, regulatory documents, and patent applications Work independently in a fast paced, multi-tasking environment as part of a diverse research team. Collaborate with cross-functional teams to advance programs from early discovery to preclinical development Qualifications: Qualifications Required: Bachelor's Degree with 5 years of experience, or

Director, Country Clinical Operations Management Bengaluru, KA, India Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Country Clinical Operations Manager is the key leader for Clinical Operations at the country level for both internal & external partners. Accountable for the strategic and operational management for clinical operations and clinical site management activities for the assigned country/ies. Responsible for leading the implementation of the corporate vision and objectives, operating across all therapeutics areas to support the execution of AbbVie's pipeline. The role is accountable for country clinical trial performance, providing strategic planning, oversight and direction of the country team to ensure on time, within budget and quality delivery of internally conducted clinical studies. The Country COM is accountable to develop a highly collaborative framework with internal and external key stakeholders across the local and global organization to best position AbbVie in advancing clinical research and accelerating the transformation of science into best-in-class medicines. •Defines the country strategy and operational plans aligned with AbbVie's business priorities, Clinical Development Operations and affiliate objectives in order to position the

Senior Specialist or Manager,Medical Strategic Operations(Medical Information) Minato City, Tokyo, Japan 企業概要: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. 求人内容: Senior Specialist サマリー： このポジションは、実務担当者として、インタビューフォームやくすりのしおり等の資材作成の他、薬剤のプロモーション前に病院薬剤部が実施するヒアリングに必要な資料の整備など、日本のregulation上必要なメディカルインフォメーション（MI）業務を行い、新薬の上市と発売後の薬剤の適正使用をサポートします。また、Global Medical Information （GMI）の目標達成のために、Large Business Unit （LBU）に戦略的・運用的サポートの提供や、GMIとAlignしながら、Regional MIチームと連携し、Affiliateにおける業務を行います。Best Practiceへの助言やAffiliateにおける分析レポートのステークホルダーへの共有、MIプロセスに関するトレーニング、ファーマコビジランス、製品監視、その他の関連関係者との連絡役も担います。また、メディカルにおけるデジタル化推進やその他のメディカルオペレーション業務なども担当します。 主な職責： 日本 の regulation で求められる MI の役割： 「インタビューフォーム」や「くすりのしおり」など、規制上必須となる資料の作成を主導し、それぞれ医薬品医療機器総合機構（PMDA）および薬剤リスク・ベネフィット評価分析・対応（RAD-AR）機構へ情報・資料を提出する 添付文書の改訂や新たな適応追加に応じて、これらの資料を適宜更新する コマーシャル部門による販促活動前に必須となる、病院薬剤部による薬剤ヒアリングに必要な資料を整備し、営業部門による製品上市活動を支援する。 国内事項の MI 専門家としての役割： データプライバシー、ファーマコビジランス、規制諸業務等についてのローカルビジネスに精通し、データプライバシーに関するregulationの情報をRegional MIデータベースへ提供する 日本国内のregulationや組織ポリシー遵守のための指導やサポートを行う MI機能・プロセス強化のためのデジタルソリューション導入やその統括を行う 問い合わせデータを分析し、insight抽出を行い、分析レポートを作成する Regionおよび国内ステークホルダーへinsightや、問い合わせ傾向、重要トピックを共有する Insightや重要な問い合わせに関する日本国内のフィードバックをGMIへ共有する トレーニングやフォーラムの実施： 必要に応じて国内チーム向けに、MIトレーニングを企画し実施する。 Regional MIチームと連携し、プロセス・規制・GMI目標の変化に合わせてトレーニング教材を定期更新する MIフォーラムや、国内メディカルアフェアーズ、国内メディカルオペレーションの会議などに積極的に参加し、インサイトやベストプラクティス、重要情報を共有する その他メディカルオペレーション業務： メディカルアフェアーズ/オペレーションリーダーの要請に応じ、その他ローカルの業務へ対応する 業務に必要な費用の把握と予算に応じたプロジェクトの実行 Manager サマリー： このポジションは、実務担当者として、インタビューフォームやくすりのしおり等の資材作成の他、薬剤のプロモーション前に病院薬剤部が実施するヒアリングに必要な資料の整備など、日本のregulation上必要なメディカルインフォメーション（MI）業務を行い、新薬の上市と発売後の薬剤の適正使用をサポートします。また、Global Medical Information （GMI）の目標達成のために、Large Business Unit （LBU）に戦略的・運用的サポートの提供や、GMIとAlignしながら、Regional MIチームと連携し、Affiliateにおける業務を行います。Best Practiceへの助言やAffiliateにおける分析レポートのステークホルダーへの共有、MIプロセスに関するトレーニング、ファーマコビジランス、製品監視、その他の関連関係者との連絡役も担います。また、メディカルにおけるデジタル化推進やその他のメディカルオペレーション業務なども担当します。 主な職責： 日本 の regulation で求められる MI の役割： 「インタビューフォーム」や「くすりのしおり」など、規制上必須となる資料の作成を主導し、それぞれ医薬品医療機器総合機構（PMDA）および薬剤リスク・ベネフィット評価分析・対応（RAD-AR）機構へ情報・資料を提出する 添付文書の改訂や新たな適応追加に応じて、これらの資料を適宜更新する コマーシャル部門による販促活動前に必須となる、病院薬剤部による薬剤ヒアリングに必要な資料を整備し、営業部門による製品上市活動を支援する。 国内事項の MI 専門家としての役割： データプライバシー、ファーマコビジランス、規制諸業務等についてのローカルビジネスに精通し、データプライバシーに関するregulationの情報をRegional MIデータベースへ提供する 日本国内のregulationや組織ポリシー遵守のための指導やサポートを行う MI機能・プロセス強化のためのデジタルソリューション導入やその統括を行う 問い合わせデータを分析し、insight抽出を行い、分析レポートを作成する Regionおよび国内ステークホルダーへinsightや、問い合わせ傾向、重要トピックを共有する Insightや重要な問い合わせに関する日本国内のフィードバックをGMIへ共有する トレーニングやフォーラムの実施： 必要に応じて国内チーム向けに、MIトレーニングを企画し実施する。 Regional MIチームと連携し、プロセス・規制・GMI目標の変化に合わせてトレーニング教材を定期更新する MIフォーラムや、国内メディカルアフェアーズ、国内メディカルオペレーションの会議などに積極的に参加し、インサイトやベストプラクティス、重要情報を共有する その他メディカルオペレーション業務： メディカルアフェアーズ/オペレーションリーダーの要請に応じ、その他ローカルの業務へ対応する 業務に必要な費用の把握と予算に応じたプロジェクトの実行 資格: Senior Specialist 必須スキル・経験 細部への注意力、優れた分析力、明確・簡潔な口頭および書面コミュニケーション能力 クリティカルシンキングで医療情報資料の調査・分析・評価、関連する指示・ポリシー・ガイドラインの解釈・適用 医薬品の原則と実務、その応用、医療用語や治療法、薬理学分野の知識・理論・応用能力 プロセス改善・高品質基準維持の推進力 関係部門や外部ベンダーとの調整・コミュニケーション能力 地域横断プロジェクトを主導した経験や多様なチーム間の調整力 文化・医療/臨床実践の差異への感受性 英語によるコミュニケーション能力 応募資格 理系または、医療系の学士を有していること、かつ、2年以上の製薬企業での勤務経験、または、医療分野4年以上の勤務経験を有していること。PhDであれば尚可 インターン・レジデンシー経験も可。 博士号（PharmD, PhD）に加えて、製薬等の実務経験3年以上あれば尚可。 最新の規制（欧州医薬品庁、PMDA、FDA等）やAbbVie治療領域・研究領域への知識があれば尚可 Manager 必須スキル・経験 細部への注意力、優れた分析力、明確・簡潔な口頭および書面コミュニケーション能力 クリティカルシンキングで医療情報資料の調査・分析・評価、関連する指示・ポリシー・ガイドラインの解釈・適用 医薬品の原則と実務、その応用、医療用語や治療法、薬理学分野の知識・理論・応用能力 プロセス改善・高品質基準維持の推進力 関係部門や外部ベンダーとの調整・コミュニケーション能力 地域横断プロジェクトを主導した経験や多様なチーム間の調整力 文化・医療/臨床実践の差異への感受性 英語によるコミュニケーション能力 チームマネジャーのサポートおよびチーム員のスキルアップ 応募資格 理系または、医療系の学士を有していること、かつ、2年以上の製薬企業での勤務経験、または、医療分野4年以上の勤務経験を有していること。PhDであれば尚可 インターン・レジデンシー経験も可。 博士号（PharmD, PhD）に加えて、製薬等の実務経験3年以上あれば尚可。 最新の規制（欧州医薬品庁、PMDA、FDA等）やAbbVie治療領域・研究領域への知識があれば尚可。 共通 マインド： 患者さん中心/Patient Centric One AbbVieとして/All for one AbbVie 賢明かつ確実な判断/Decide Smart and Sure 迅速性と責任感/Agile and Accountable 明確に、そして勇敢に/Clear and Courageous 可能性の実現/Make Possibilities Real インテグリティ/Integrity その他の情報: 経験値、面接結果により「Specialist(G14)」での合格となる場合があります。 アッヴィは、機会均等を重視する雇用主であり、誠実な企業活動、革新の推進、人々の生活への貢献、そして地域社会への貢献に努めています。雇用機会均等に向けて、障がいを持つ方々も積極的に支援しています。