Large

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.  

Science & Healthcare

AbbVie

You must have a PhD in a related field, experience with AAVs, proficiency in analytical methods, and strong communication skills. Experience in CMC teams is a plus. Fluency in English required.

You will develop stable formulations, manage teams, document experiments, report progress, prepare regulatory submissions, mentor junior scientists, and maintain lab equipment.

Science

Research & Development

Ludwigshafen

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 At AbbVie, we strive to push the boundaries of science and innovation to improve life quality globally. As part of our vibrant team, you'll help transform the possibilities in neurological and psychiatric care into realities. Join a global powerhouse with over 50,000 employees worldwide, including 3,000 in Germany, where your expertise will address tomorrow's unmet medical needs. Join our team in the development of adeno-associated virus (AAV) formulations for gene therapy applications and other modalities such as monoclonal antibodies in the field of biopharmaceuticals. Make your mark by: * Drive the development of stable formulations. Design and execute experiments in the lab to characterize and optimize formulation candidates and demonstrate suitability of methods. Identify and implement the best-suited analytical methodologies. * Initiate, collaborate and manage local and international teams, including Discovery, Analytics, Container Closure Sciences, and Process Development. Collaborate closely with cross-functional Chemistry, Manufacturing, and Controls (CMC) teams to ensure alignment on project goals and timelines. Participate in CMC teams as representative of drug product development. * Contribute in establishing AAV formulation development capabilities (i.e., lab infrastructure and analytical instruments). Work alongside experts from various disciplines, utilizing cutting-edge equipment, and adapting to emerging technologies and challenges. * Document experiments and results clearly and accurately in electronic laboratory notebooks. * Report on experimental work and progress to peers, management, and partnering stakeholders. * Prepare and contribute to essential documentation for regulatory submissions. * Stay updated on advances in formulation development strategies and technologies, including attendance at relevant conferences. * Identify and develop novel methods in partnership with the analytical development team. * Prepare patents and manuscripts for publication in scientific journals and contribute to scientific dialogue within AbbVie’s global scientific community. * Mentor junior scientists, sharing knowledge and best practices in AAV development. * Manage and maintain lab equipment and supplies, ensuring a safe and efficient work environment. Qualifications This is how you can make a difference: * PhD or equivalent education in pharmacy, virology, biotechnology, biology, or related fields. Practical experience is a plus, optimally in an industrial environment. Experience in development work / analytics with AAVs is a significant plus. * Proficiency in common analytical methods for biopharmaceutical products, including but not limited to Dynamic Light Scattering, Liquid Chromatography, Capillary Electrophoresis, Plate-based Binding Assays, Spectrophotometry, osmometry, viscosimetry, etc. * Proven track record of conducting high-quality research, encompassing experimental design, data analysis, and interpretation. * Experience in authoring technical reports in English, including data interpretation for regulatory submissions. * Strong communication and team collaboration skills to effectively contribute to multidisciplinary team environments and collaborative research projects. * Experience with working in CMC teams is a plus. * Personal initiative and problem-solving capabilities to develop innovative solutions within pharmaceutical development challenges. * Strong written and verbal communication skills, with a demonstrated ability to publish and present scientific results. * Fluency in English is mandatory, German language knowledge is a plus What we offer you: * with a diverse work environment where you can have a real impact * with an open corporate culture * with an attractive salary * with an intensive onboarding process with a mentor at your side * with flexible work models for a healthy work-life balance * with a corporate health management that offers comprehensive health and exercise programs * with company social benefits * with a wide range of career opportunities in an international organization * with top-tier, attractive development opportunities * with a strong international network Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Company DescriptionAbbVie'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 DescriptionAt AbbVie, we strive to push the boundaries of science and innovation to improve life quality globally. As part of our vibrant team, you'll help transform the possibilities in neurological and psychiatric care into realities. Join a global powerhouse with over 50,000 employees worldwide, including 3,000 in Germany, where your expertise will address tomorrow's unmet medical needs.Join our team in the development of adeno-associated virus (AAV) formulations for gene therapy applications and other modalities such as monoclonal antibodies in the field of biopharmaceuticals.Make your mark by: * Drive the development of stable formulations. Design and execute experiments in the lab to characterize and optimize formulation candidates and demonstrate suitability of methods. Identify and implement the best-suited analytical methodologies. * Initiate, collaborate and manage local and international teams, including Discovery, Analytics, Container Closure Sciences, and Process Development. Collaborate closely with cross-functional Chemistry, Manufacturing, and Controls (CMC) teams to ensure alignment on project goals and timelines. Participate in CMC teams as representative of drug product development. * Contribute in establishing AAV formulation development capabilities (i.e., lab infrastructure and analytical instruments). Work alongside experts from various disciplines, utilizing cutting-edge equipment, and adapting to emerging technologies and challenges. * Document experiments and results clearly and accurately in electronic laboratory notebooks. * Report on experimental work and progress to peers, management, and partnering stakeholders. * Prepare and contribute to essential documentation for regulatory submissions. * Stay updated on advances in formulation development strategies and technologies, including attendance at relevant conferences. * Identify and develop novel methods in partnership with the analytical development team. * Prepare patents and manuscripts for publication in scientific journals and contribute to scientific dialogue within AbbVie’s global scientific community. * Mentor junior scientists, sharing knowledge and best practices in AAV development. * Manage and maintain lab equipment and supplies, ensuring a safe and efficient work environment.      QualificationsThis is how you can make a difference: * PhD or equivalent education in pharmacy, virology, biotechnology, biology, or related fields. Practical experience is a plus, optimally in an industrial environment. Experience in development work / analytics with AAVs is a significant plus. * Proficiency in common analytical methods for biopharmaceutical products, including but not limited to Dynamic Light Scattering, Liquid Chromatography, Capillary Electrophoresis, Plate-based Binding Assays, Spectrophotometry, osmometry, viscosimetry, etc. * Proven track record of conducting high-quality research, encompassing experimental design, data analysis, and interpretation. * Experience in authoring technical reports in English, including data interpretation for regulatory submissions. * Strong communication and team collaboration skills to effectively contribute to multidisciplinary team environments and collaborative research projects. * Experience with working in CMC teams is a plus. * Personal initiative and problem-solving capabilities to develop innovative solutions within pharmaceutical development challenges. * Strong written and verbal communication skills, with a demonstrated ability to publish and present scientific results. * Fluency in English is mandatory, German language knowledge is a plus      What we offer you: * with a diverse work environment where you can have a real impact * with an open corporate culture * with an attractive salary * with an intensive onboarding process with a mentor at your side * with flexible work models for a healthy work-life balance * with a corporate health management that offers comprehensive health and exercise programs * with company social benefits * with a wide range of career opportunities in an international organization * with top-tier, attractive development opportunities * with a strong international network      Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.Additional InformationAbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html

Senior Scientist I – Genetic Medicine Drug Product Development (all genders) (fulltime, permanent) - AbbVie

&lt;strong&gt;Company Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;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.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;At AbbVie, we strive to push the boundaries of science and innovation to improve life quality globally. As part of our vibrant team, you'll help transform the possibilities in neurological and psychiatric care into realities. Join a global powerhouse with over 50,000 employees worldwide, including 3,000 in Germany, where your expertise will address tomorrow's unmet medical needs.&lt;br&gt;&lt;br&gt;Join our team in the development of adeno-associated virus (AAV) formulations for gene therapy applications and other modalities such as monoclonal antibodies in the field of biopharmaceuticals.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Make your mark by:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Drive the development of stable formulations. Design and execute experiments in the lab to characterize and optimize formulation candidates and demonstrate suitability of methods. Identify and implement the best-suited analytical methodologies.&lt;/li&gt;&lt;li&gt;Initiate, collaborate and manage local and international teams, including Discovery, Analytics, Container Closure Sciences, and Process Development. Collaborate closely with cross-functional Chemistry, Manufacturing, and Controls (CMC) teams to ensure alignment on project goals and timelines. Participate in CMC teams as representative of drug product development.&lt;/li&gt;&lt;li&gt;Contribute in establishing AAV formulation development capabilities (i.e., lab infrastructure and analytical instruments). Work alongside experts from various disciplines, utilizing cutting-edge equipment, and adapting to emerging technologies and challenges.&lt;/li&gt;&lt;li&gt;Document experiments and results clearly and accurately in electronic laboratory notebooks.&lt;/li&gt;&lt;li&gt;Report on experimental work and progress to peers, management, and partnering stakeholders.&lt;/li&gt;&lt;li&gt;Prepare and contribute to essential documentation for regulatory submissions.&lt;/li&gt;&lt;li&gt;Stay updated on advances in formulation development strategies and technologies, including attendance at relevant conferences.&lt;/li&gt;&lt;li&gt;Identify and develop novel methods in partnership with the analytical development team.&lt;/li&gt;&lt;li&gt;Prepare patents and manuscripts for publication in scientific journals and contribute to scientific dialogue within AbbVie’s global scientific community.&lt;/li&gt;&lt;li&gt;Mentor junior scientists, sharing knowledge and best practices in AAV development.&lt;/li&gt;&lt;li&gt;Manage and maintain lab equipment and supplies, ensuring a safe and efficient work environment.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;This is how you can make a difference:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;PhD or equivalent education in pharmacy, virology, biotechnology, biology, or related fields. Practical experience is a plus, optimally in an industrial environment. Experience in development work / analytics with AAVs is a significant plus.&lt;/li&gt;&lt;li&gt;Proficiency in common analytical methods for biopharmaceutical products, including but not limited to Dynamic Light Scattering, Liquid Chromatography, Capillary Electrophoresis, Plate-based Binding Assays, Spectrophotometry, osmometry, viscosimetry, etc.&lt;/li&gt;&lt;li&gt;Proven track record of conducting high-quality research, encompassing experimental design, data analysis, and interpretation.&lt;/li&gt;&lt;li&gt;Experience in authoring technical reports in English, including data interpretation for regulatory submissions.&lt;/li&gt;&lt;li&gt;Strong communication and team collaboration skills to effectively contribute to multidisciplinary team environments and collaborative research projects.&lt;/li&gt;&lt;li&gt;Experience with working in CMC teams is a plus.&lt;/li&gt;&lt;li&gt;Personal initiative and problem-solving capabilities to develop innovative solutions within pharmaceutical development challenges.&lt;/li&gt;&lt;li&gt;Strong written and verbal communication skills, with a demonstrated ability to publish and present scientific results.&lt;/li&gt;&lt;li&gt;Fluency in English is mandatory, German language knowledge is a plus&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What we offer you:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;with a diverse work environment where you can have a real impact&lt;/li&gt;&lt;li&gt;with an open corporate culture&lt;/li&gt;&lt;li&gt;with an attractive salary&lt;/li&gt;&lt;li&gt;with an intensive onboarding process with a mentor at your side&lt;/li&gt;&lt;li&gt;with flexible work models for a healthy work-life balance&lt;/li&gt;&lt;li&gt;with a corporate health management that offers comprehensive health and exercise programs&lt;/li&gt;&lt;li&gt;with company social benefits&lt;/li&gt;&lt;li&gt;with a wide range of career opportunities in an international organization&lt;/li&gt;&lt;li&gt;with top-tier, attractive development opportunities&lt;/li&gt;&lt;li&gt;with a strong international network&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&amp;amp;I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.&lt;br&gt;&lt;br&gt;Additional Information&lt;br&gt;&lt;br&gt;AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:&lt;br&gt;&lt;br&gt;https://www.abbvie.com/join-us/reasonable-accommodations.html

Senior Scientist I – Genetic Medicine Drug Product Development (all genders) (fulltime, permanent)

You need an advanced life sciences degree, 3-5 years' experience, investment knowledge in early-stage biotech, strong communication skills, and the ability to work independently with minimal supervision.

You will source opportunities, evaluate deals, manage relationships, drive investment processes, and oversee portfolio companies while ensuring alignment with AbbVie stakeholders.

Business, Operations & Strategy

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 AbbVie Ventures represents the strategic investment arm of the company and a core component of AbbVie's integrated approach to external innovation. We invest in early-stage transformational scientific opportunities that augment our core R&D areas within oncology, immunology, neuroscience, ophthalmology, and aesthetics. We invest proactively to access transformative early-stage science, exceptional talent, and emerging biotech ecosystems. Our investments and interactions with fellow investors, scientists, physicians, and entrepreneurs provide us insights into novel biology and technologies that result in targeted enhancement of our scientific knowledge as well as early assessments of potential future business development opportunities. Our broad and deep expertise in drug discovery, development, manufacturing, and commercialization is a valuable resource to even the earliest stage companies. Through this proactive engagement with the scientific community, we are building our reputation as a committed leader in the biotechnology ecosystem, while supplementing our R&D pipeline in a capital-efficient manner. Responsibilities: Proactive opportunity sourcing: * Build awareness regarding AbbVie and the Venture group amongst interconnected networks of early-stage life science focused venture investors and company creators, entrepreneurs, scientific founders, and accelerators/incubators globally. * Participate in partnering meetings and conferences to identify and evaluate potential investment opportunities that are consistent with AbbVie R&D strategies. * Thoughtfully drive sustainable growth for the Company including managing and generating relationships with potential sources of opportunities and potential co-investors. Deal evaluation and execution: * Lead the assessment (in close collaboration with Search and Evaluation and Business Development) and drive the evaluation process and timeline, developing timely recommendations and proposals for senior management consideration, based on thorough technical review and unique insights. * Assist in developing effective deal structure optionality, risk mitigation and negotiation strategies and ensure alignment with AbbVie objectives and functional management. * Help drive the deal execution and investment process, including support the diligence team and cross-functional internal review to present the investment recommendation to the Investment Committee, negotiating deal documents and managing the closing process Portfolio management: * Participate in reviews and monitor AbbVie Ventures’ portfolio companies by keeping abreast of developments within the companies, building and maintaining good working relationships with executive management and the Board of Directors, and participating in Board meetings. * Serve as an additional point of contact for portfolio companies within AbbVie to ensure alignment and engagement with key internal stakeholders. Qualifications * Advanced degree in the life sciences (PhD, MD, MD/PhD) with at least 3-5 years of postgraduate experience. Drug discovery experience is preferred, but not required, with ability to work across all other AbbVie relevant core areas of interest (oncology, neuroscience, immunology, ophthalmology, aesthetics). * Investment experience in early-stage life science is preferred (focus on pre-Seed through Series B, including business incubation/company creation). * Good understanding of the drug discovery and development, regulatory, and commercialization process for evaluation of pharmaceutical opportunities; should have rigorous scientific knowledge to objectively evaluate potential business opportunities. * Exceptional talent and organizational skills to evaluate target opportunities and produce high quality analyses. Ability to drive projects to deliver timely results and follow through on commitments. * Strong communication skills to effectively communicate business strategies and capabilities internally and externally, present individual and team recommendations clearly and concisely, and promote cross-functional communication. * An established network and personal brand in the biopharma community preferred. Proactive and engaging social and networking skills to reach out to a broad range of industry decision makers to keep abreast of emerging opportunities. * Candidate must be able to act independently without daily onsite managerial supervision. This role may be based in the United Kingdom or continental Europe. The role will require domestic and international travel of ~25%. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Company DescriptionAbbVie'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 DescriptionAbbVie Ventures represents the strategic investment arm of the company and a core component of AbbVie's integrated approach to external innovation. We invest in early-stage transformational scientific opportunities that augment our core R&D areas within oncology, immunology, neuroscience, ophthalmology, and aesthetics. We invest proactively to access transformative early-stage science, exceptional talent, and emerging biotech ecosystems.Our investments and interactions with fellow investors, scientists, physicians, and entrepreneurs provide us insights into novel biology and technologies that result in targeted enhancement of our scientific knowledge as well as early assessments of potential future business development opportunities. Our broad and deep expertise in drug discovery, development, manufacturing, and commercialization is a valuable resource to even the earliest stage companies. Through this proactive engagement with the scientific community, we are building our reputation as a committed leader in the biotechnology ecosystem, while supplementing our R&D pipeline in a capital-efficient manner.Responsibilities:Proactive opportunity sourcing: * Build awareness regarding AbbVie and the Venture group amongst interconnected networks of early-stage life science focused venture investors and company creators, entrepreneurs, scientific founders, and accelerators/incubators globally. * Participate in partnering meetings and conferences to identify and evaluate potential investment opportunities that are consistent with AbbVie R&D strategies. * Thoughtfully drive sustainable growth for the Company including managing and generating relationships with potential sources of opportunities and potential co-investors.      Deal evaluation and execution: * Lead the assessment (in close collaboration with Search and Evaluation and Business Development) and drive the evaluation process and timeline, developing timely recommendations and proposals for senior management consideration, based on thorough technical review and unique insights. * Assist in developing effective deal structure optionality, risk mitigation and negotiation strategies and ensure alignment with AbbVie objectives and functional management. * Help drive the deal execution and investment process, including support the diligence team and cross-functional internal review to present the investment recommendation to the Investment Committee, negotiating deal documents and managing the closing process      Portfolio management: * Participate in reviews and monitor AbbVie Ventures’ portfolio companies by keeping abreast of developments within the companies, building and maintaining good working relationships with executive management and the Board of Directors, and participating in Board meetings. * Serve as an additional point of contact for portfolio companies within AbbVie to ensure alignment and engagement with key internal stakeholders.      Qualifications * Advanced degree in the life sciences (PhD, MD, MD/PhD) with at least 3-5 years of postgraduate experience. Drug discovery experience is preferred, but not required, with ability to work across all other AbbVie relevant core areas of interest (oncology, neuroscience, immunology, ophthalmology, aesthetics). * Investment experience in early-stage life science is preferred (focus on pre-Seed through Series B, including business incubation/company creation). * Good understanding of the drug discovery and development, regulatory, and commercialization process for evaluation of pharmaceutical opportunities; should have rigorous scientific knowledge to objectively evaluate potential business opportunities. * Exceptional talent and organizational skills to evaluate target opportunities and produce high quality analyses. Ability to drive projects to deliver timely results and follow through on commitments. * Strong communication skills to effectively communicate business strategies and capabilities internally and externally, present individual and team recommendations clearly and concisely, and promote cross-functional communication. * An established network and personal brand in the biopharma community preferred. Proactive and engaging social and networking skills to reach out to a broad range of industry decision makers to keep abreast of emerging opportunities. * Candidate must be able to act independently without daily onsite managerial supervision. This role may be based in the United Kingdom or continental Europe. The role will require domestic and international travel of ~25%.      Additional InformationAbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html

Associate Director, Ventures (all genders) (fulltime, permanent) - AbbVie

&lt;strong&gt;Company Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;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.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;AbbVie Ventures represents the strategic investment arm of the company and a core component of AbbVie's integrated approach to external innovation. We invest in early-stage transformational scientific opportunities that augment our core R&amp;amp;D areas within oncology, immunology, neuroscience, ophthalmology, and aesthetics. We invest proactively to access transformative early-stage science, exceptional talent, and emerging biotech ecosystems.&lt;br&gt;&lt;br&gt;Our investments and interactions with fellow investors, scientists, physicians, and entrepreneurs provide us insights into novel biology and technologies that result in targeted enhancement of our scientific knowledge as well as early assessments of potential future business development opportunities. Our broad and deep expertise in drug discovery, development, manufacturing, and commercialization is a valuable resource to even the earliest stage companies. Through this proactive engagement with the scientific community, we are building our reputation as a committed leader in the biotechnology ecosystem, while supplementing our R&amp;amp;D pipeline in a capital-efficient manner.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;Proactive opportunity sourcing: &lt;br&gt;&lt;br&gt;&lt;/em&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Build awareness regarding AbbVie and the Venture group amongst interconnected networks of early-stage life science focused venture investors and company creators, entrepreneurs, scientific founders, and accelerators/incubators globally.&lt;/li&gt;&lt;li&gt;Participate in partnering meetings and conferences to identify and evaluate potential investment opportunities that are consistent with AbbVie R&amp;amp;D strategies.&lt;/li&gt;&lt;li&gt;Thoughtfully drive sustainable growth for the Company including managing and generating relationships with potential sources of opportunities and potential co-investors.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;&lt;em&gt;Deal evaluation and execution:&lt;br&gt;&lt;br&gt;&lt;/em&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Lead the assessment (in close collaboration with Search and Evaluation and Business Development) and drive the evaluation process and timeline, developing timely recommendations and proposals for senior management consideration, based on thorough technical review and unique insights.&lt;/li&gt;&lt;li&gt;Assist in developing effective deal structure optionality, risk mitigation and negotiation strategies and ensure alignment with AbbVie objectives and functional management.&lt;/li&gt;&lt;li&gt;Help drive the deal execution and investment process, including support the diligence team and cross-functional internal review to present the investment recommendation to the Investment Committee, negotiating deal documents and managing the closing process&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Portfolio management: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Participate in reviews and monitor AbbVie Ventures’ portfolio companies by keeping abreast of developments within the companies, building and maintaining good working relationships with executive management and the Board of Directors, and participating in Board meetings.&lt;/li&gt;&lt;li&gt;Serve as an additional point of contact for portfolio companies within AbbVie to ensure alignment and engagement with key internal stakeholders. &lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Advanced degree in the life sciences (PhD, MD, MD/PhD) with at least 3-5 years of postgraduate experience. Drug discovery experience is preferred, but not required, with ability to work across all other AbbVie relevant core areas of interest (oncology, neuroscience, immunology, ophthalmology, aesthetics).&lt;/li&gt;&lt;li&gt;Investment experience in early-stage life science is preferred (focus on pre-Seed through Series B, including business incubation/company creation).&lt;/li&gt;&lt;li&gt;Good understanding of the drug discovery and development, regulatory, and commercialization process for evaluation of pharmaceutical opportunities; should have rigorous scientific knowledge to objectively evaluate potential business opportunities.&lt;/li&gt;&lt;li&gt;Exceptional talent and organizational skills to evaluate target opportunities and produce high quality analyses. Ability to drive projects to deliver timely results and follow through on commitments.&lt;/li&gt;&lt;li&gt;Strong communication skills to effectively communicate business strategies and capabilities internally and externally, present individual and team recommendations clearly and concisely, and promote cross-functional communication.&lt;/li&gt;&lt;li&gt;An established network and personal brand in the biopharma community preferred. Proactive and engaging social and networking skills to reach out to a broad range of industry decision makers to keep abreast of emerging opportunities.&lt;/li&gt;&lt;li&gt;Candidate must be able to act independently without daily onsite managerial supervision. This role may be based in the United Kingdom or continental Europe. The role will require domestic and international travel of ~25%.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Additional Information&lt;br&gt;&lt;br&gt;AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:&lt;br&gt;&lt;br&gt;https://www.abbvie.com/join-us/reasonable-accommodations.html

Associate Director, Ventures (all genders) (fulltime, permanent)

You need an Accounting/Finance degree, 8+ years' experience in FP&A, team leadership, strong analytical and communication skills, Excel proficiency, and SAP knowledge.

You will manage a team, oversee financial reporting, provide insights on risks and opportunities, and support R&D finance strategy through detailed analyses and recommendations.

Accounting & Tax

Unternehmensbeschreibung 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. Stellenbeschreibung The job that makes possibilities real in patients' lives. And yours. The job that helps you get ahead in life. Moving mountains together. As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? You have come to the right place! Moving mountains together – as Director Controlling R&D Ludwigshafen (all genders) (permanent / full-time) Responsibilities * Reporting to Sr Finance Director R&D. * Manage and develop a team of 11, including people managers and analysts. * Key contact person for all Ludwigshafen R&D Finance related items. * Oversee monthly / quarterly fincancial close, monthly LBES (latest best estimates), annual plan and LRP (long range plans), for all Ludwigshafen R&D financials * Provides detailed information and recommendations to R&D Controlling HQ Management for making decisions with potential impacts on global R&D performance. * Provide insights to R&D leadership on risks and opportunities based on the understanding of financial results and forecasts, driving AbbVie R&D and Finance strategy. Qualifikationen * Accounting / Finance Degree Required. * Minimum 8+ years of progressive and related experience. Experience in financial planning and analysis. * Experience in coaching / leading a team. * Strong financial, analytical and problem-solving skills. * Strong communication skills (verbal and written), with all levels of management. * Ability to operate independently, drive processes, identify and implement process improvements, establish and adjust priorities to achieve objectives and operate with speed and agility. * Proficient Excel skills. * Knowledge of SAP. Here's How We Can Move Mountains Together * with a diverse work environment where you can have a real impact * with an open corporate culture * with an attractive salary * with an intensive onboarding process with a mentor at your side * with flexible work models for a healthy work-life balance * with a corporate health management that offers comprehensive health and exercise programs * with company social benefits * with a wide range of career opportunities in an international organization * with top-tier, attractive development opportunities * with a strong international network Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect. At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person. Have questions? Email talentacquisition.de@abbvie.com – we look forward to hearing from you! Zusätzliche Informationen Only together can we achieve the best for patients. That's why we at AbbVie focus on equal opportunity, diversity & inclusion. We create a work environment in which all employees can develop their potential — regardless of gender, origin, religion, sexual orientation or other dimensions of diversity. But for us, diversity means more than just taking obvious differences into account: It also relates to different educational backgrounds, expertise, personality types, ways of thinking and life experiences. Nur gemeinsam können wir das Beste für Patienten erreichen. Daher setzen wir bei AbbVie auf Chancengleichheit, Vielfalt & Inklusion. Wir gestalten ein Arbeitsumfeld, in dem alle Mitarbeiter ihr Potenzial entfalten können – unabhängig von Geschlecht, Herkunft, Religion, sexueller Orientierung oder anderen Vielfaltsdimensionen. Doch für uns bedeutet Vielfalt mehr als nur offensichtliche Unterschiede zu berücksichtigen: Sie bezieht sich auch auf unterschiedliche Ausbildungshintergründe, Fachkenntnisse, Persönlichkeitstypen, Denkweisen und Lebenserfahrungen.

UnternehmensbeschreibungAbbVie'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.StellenbeschreibungThe job that makes possibilities real in patients' lives. And yours.The job that helps you get ahead in life. Moving mountains together.As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? You have come to the right place!Moving mountains together – as Director Controlling R&D Ludwigshafen (all genders) (permanent / full-time)Responsibilities * Reporting to Sr Finance Director R&D. * Manage and develop a team of 11, including people managers and analysts. * Key contact person for all Ludwigshafen R&D Finance related items. * Oversee monthly / quarterly fincancial close, monthly LBES (latest best estimates), annual plan and LRP (long range plans), for all Ludwigshafen R&D financials * Provides detailed information and recommendations to R&D Controlling HQ Management for making decisions with potential impacts on global R&D performance. * Provide insights to R&D leadership on risks and opportunities based on the understanding of financial results and forecasts, driving AbbVie R&D and Finance strategy.      Qualifikationen * Accounting / Finance Degree Required. * Minimum 8+ years of progressive and related experience. Experience in financial planning and analysis. * Experience in coaching / leading a team. * Strong financial, analytical and problem-solving skills. * Strong communication skills (verbal and written), with all levels of management. * Ability to operate independently, drive processes, identify and implement process improvements, establish and adjust priorities to achieve objectives and operate with speed and agility. * Proficient Excel skills. * Knowledge of SAP.      Here's How We Can Move Mountains Together * with a diverse work environment where you can have a real impact * with an open corporate culture * with an attractive salary * with an intensive onboarding process with a mentor at your side * with flexible work models for a healthy work-life balance * with a corporate health management that offers comprehensive health and exercise programs * with company social benefits * with a wide range of career opportunities in an international organization * with top-tier, attractive development opportunities * with a strong international network      Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person.Have questions? Email talentacquisition.de@abbvie.com – we look forward to hearing from you!Zusätzliche InformationenOnly together can we achieve the best for patients. That's why we at AbbVie focus on equal opportunity, diversity & inclusion. We create a work environment in which all employees can develop their potential — regardless of gender, origin, religion, sexual orientation or other dimensions of diversity. But for us, diversity means more than just taking obvious differences into account: It also relates to different educational backgrounds, expertise, personality types, ways of thinking and life experiences.Nur gemeinsam können wir das Beste für Patienten erreichen. Daher setzen wir bei AbbVie auf Chancengleichheit, Vielfalt & Inklusion. Wir gestalten ein Arbeitsumfeld, in dem alle Mitarbeiter ihr Potenzial entfalten können – unabhängig von Geschlecht, Herkunft, Religion, sexueller Orientierung oder anderen Vielfaltsdimensionen. Doch für uns bedeutet Vielfalt mehr als nur offensichtliche Unterschiede zu berücksichtigen: Sie bezieht sich auch auf unterschiedliche Ausbildungshintergründe, Fachkenntnisse, Persönlichkeitstypen, Denkweisen und Lebenserfahrungen.

Director Controlling R&D Ludwigshafen (all genders) (permanent / full-time) - AbbVie

Unternehmensbeschreibung&lt;br&gt;&lt;br&gt;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.&lt;br&gt;&lt;br&gt;Stellenbeschreibung&lt;br&gt;&lt;br&gt;&lt;strong&gt;The job that makes possibilities real in patients' lives. And yours.&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;The job that helps you get ahead in life. Moving mountains together.&lt;br&gt;&lt;br&gt;&lt;/strong&gt;As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? You have come to the right place!&lt;br&gt;&lt;br&gt;Moving mountains together – as&lt;strong&gt; Director Controlling R&amp;amp;D Ludwigshafen (all genders) (permanent / full-time)&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Reporting to Sr Finance Director R&amp;amp;D.&lt;/li&gt;&lt;li&gt;Manage and develop a team of 11, including people managers and analysts.&lt;/li&gt;&lt;li&gt;Key contact person for all Ludwigshafen R&amp;amp;D Finance related items.&lt;/li&gt;&lt;li&gt;Oversee monthly / quarterly fincancial close, monthly LBES (latest best estimates), annual plan and LRP (long range plans), for all Ludwigshafen R&amp;amp;D financials&lt;/li&gt;&lt;li&gt;Provides detailed information and recommendations to R&amp;amp;D Controlling HQ Management for making decisions with potential impacts on global R&amp;amp;D performance.&lt;/li&gt;&lt;li&gt;Provide insights to R&amp;amp;D leadership on risks and opportunities based on the understanding of financial results and forecasts, driving AbbVie R&amp;amp;D and Finance strategy.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Qualifikationen&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;Accounting / Finance Degree Required.&lt;/li&gt;&lt;li&gt;Minimum 8+ years of progressive and related experience. Experience in financial planning and analysis.&lt;/li&gt;&lt;li&gt;Experience in coaching / leading a team.&lt;/li&gt;&lt;li&gt;Strong financial, analytical and problem-solving skills.&lt;/li&gt;&lt;li&gt;Strong communication skills (verbal and written), with all levels of management.&lt;/li&gt;&lt;li&gt;Ability to operate independently, drive processes, identify and implement process improvements, establish and adjust priorities to achieve objectives and operate with speed and agility.&lt;/li&gt;&lt;li&gt;Proficient Excel skills.&lt;/li&gt;&lt;li&gt;Knowledge of SAP.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Here's How We Can Move Mountains Together&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;with a diverse work environment where you can have a real impact &lt;/li&gt;&lt;li&gt;with an open corporate culture&lt;/li&gt;&lt;li&gt;with an attractive salary&lt;/li&gt;&lt;li&gt;with an intensive onboarding process with a mentor at your side&lt;/li&gt;&lt;li&gt;with flexible work models for a healthy work-life balance&lt;/li&gt;&lt;li&gt;with a corporate health management that offers comprehensive health and exercise programs&lt;/li&gt;&lt;li&gt;with company social benefits&lt;/li&gt;&lt;li&gt;with a wide range of career opportunities in an international organization&lt;/li&gt;&lt;li&gt;with top-tier, attractive development opportunities&lt;/li&gt;&lt;li&gt;with a strong international network&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&amp;amp;I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.&lt;br&gt;&lt;br&gt;At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person.&lt;br&gt;&lt;br&gt;Have questions? Email talentacquisition.de@abbvie.com – we look forward to hearing from you!&lt;br&gt;&lt;br&gt;Zusätzliche Informationen&lt;br&gt;&lt;br&gt;Only together can we achieve the best for patients. That's why we at AbbVie focus on equal opportunity, diversity &amp;amp; inclusion. We create a work environment in which all employees can develop their potential — regardless of gender, origin, religion, sexual orientation or other dimensions of diversity. But for us, diversity means more than just taking obvious differences into account: It also relates to different educational backgrounds, expertise, personality types, ways of thinking and life experiences.&lt;br&gt;&lt;br&gt;Nur gemeinsam können wir das Beste für Patienten erreichen. Daher setzen wir bei AbbVie auf Chancengleichheit, Vielfalt &amp;amp; Inklusion. Wir gestalten ein Arbeitsumfeld, in dem alle Mitarbeiter ihr Potenzial entfalten können – unabhängig von Geschlecht, Herkunft, Religion, sexueller Orientierung oder anderen Vielfaltsdimensionen. Doch für uns bedeutet Vielfalt mehr als nur offensichtliche Unterschiede zu berücksichtigen: Sie bezieht sich auch auf unterschiedliche Ausbildungshintergründe, Fachkenntnisse, Persönlichkeitstypen, Denkweisen und Lebenserfahrungen.

Director Controlling R&amp;D Ludwigshafen (all genders) (permanent / full-time)

Director Controlling R&D Ludwigshafen (all genders) (permanent / full-time)

You have an MSc in Engineering, Chemistry, or Pharmacy, 8+ years in process development/manufacturing, 4+ years in project management, strong GMP experience, and fluency in German and English.

You will develop project plans, manage risks, ensure quality compliance, create business cases, and update teams and executives on program status and outcomes.

Engineering

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 Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Looking for challenges where you can grow? We Offer That! Welcome to AbbVie! As part of an international company with 50,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity to work closely with us to address the health challenges of tomorrow. Do you have a passion for improving health care around the world and for using your expertise to improve patients' quality of life? In a challenging work environment that allows you to broaden and develop your own skills? You’ve found the right place! In our Tech Ops Department at Ludwigshafen site, you will join a team of talented people and experienced experts in the manufacturing, packaging, engineering and global distribution of our approved and pipeline products – working with some of the most advanced technologies in the world. Develop your expertise and join our team as Senior Program Manager TO (all genders) for global projects. You will be leading a cross-functional matrix team with integrity and respect, deliver results, champion change, foster collaboration, and teamwork, engage, and inspire. Make an impact: * Develop project plans and timelines for new product introduction of innovative pipeline assets or tech transfers of established products - in alignment with the global strategy * Maintain operational awareness of the deliverables and upcoming needs to proactively identify, communicate and manage team risks, including escalation as appropriate with a strategic, cross-functional mindset * Ensure consistency and quality and financial compliance across all aspects of assigned programs * Develop business cases together with a cross-functional team and define recommendations that are specific and measurable * Routinely update cross-functional teams on status and changes as well as present Program updates and outcomes to executive management Qualifications This is how you can make a difference: * Technical background – Master of Science in Engineering, Chemistry or Pharmacy preferred * 8+ years of experience in positions related to process development, engineering/process support or manufacturing ideally in pharmaceutical packaging * 4+ years of experience in management of global projects and programs * Expertise in project management tools (e. g. Microsoft Excel, MS project and PowerPoint) * Strong GMP experience in pharmaceutical environment * Excellent verbal and written communication skills with demonstrated ability to communicate effectively to senior management * German and English both business fluent mandatory * Ability to develop and manage financial related elements of a project; strong business acumen including project and cost accounting Here's how we can grow together: * with a diverse work environment where you can have a real impact * with an open corporate culture * with an attractive salary * with an intensive onboarding process with a mentor at your side * with flexible work models for a healthy work-life balance * with a corporate health management that offers comprehensive health and exercise programs * with company social benefits * with a wide range of career opportunities in an international organization * with top-tier, attractive development opportunities * with a strong international network At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person. Any questions? Feel free to email as at TalentAcquisition.de@abbvie.com – we look forward to hearing from you! Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Company DescriptionAbbVie'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 Twitter, Facebook, Instagram, YouTube and LinkedIn.Job DescriptionLooking for challenges where you can grow? We Offer That!Welcome to AbbVie! As part of an international company with 50,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity to work closely with us to address the health challenges of tomorrow. Do you have a passion for improving health care around the world and for using your expertise to improve patients' quality of life? In a challenging work environment that allows you to broaden and develop your own skills? You’ve found the right place!In our Tech Ops Department at Ludwigshafen site, you will join a team of talented people and experienced experts in the manufacturing, packaging, engineering and global distribution of our approved and pipeline products – working with some of the most advanced technologies in the world.Develop your expertise and join our team as Senior Program Manager TO (all genders) for global projects. You will be leading a cross-functional matrix team with integrity and respect, deliver results, champion change, foster collaboration, and teamwork, engage, and inspire.Make an impact: * Develop project plans and timelines for new product introduction of innovative pipeline assets or tech transfers of established products - in alignment with the global strategy * Maintain operational awareness of the deliverables and upcoming needs to proactively identify, communicate and manage team risks, including escalation as appropriate with a strategic, cross-functional mindset * Ensure consistency and quality and financial compliance across all aspects of assigned programs * Develop business cases together with a cross-functional team and define recommendations that are specific and measurable * Routinely update cross-functional teams on status and changes as well as present Program updates and outcomes to executive management      QualificationsThis is how you can make a difference: * Technical background – Master of Science in Engineering, Chemistry or Pharmacy preferred * 8+ years of experience in positions related to process development, engineering/process support or manufacturing ideally in pharmaceutical packaging * 4+ years of experience in management of global projects and programs * Expertise in project management tools (e. g. Microsoft Excel, MS project and PowerPoint) * Strong GMP experience in pharmaceutical environment * Excellent verbal and written communication skills with demonstrated ability to communicate effectively to senior management * German and English both business fluent mandatory * Ability to develop and manage financial related elements of a project; strong business acumen including project and cost accounting      Here's how we can grow together: * with a diverse work environment where you can have a real impact * with an open corporate culture * with an attractive salary * with an intensive onboarding process with a mentor at your side * with flexible work models for a healthy work-life balance * with a corporate health management that offers comprehensive health and exercise programs * with company social benefits * with a wide range of career opportunities in an international organization * with top-tier, attractive development opportunities * with a strong international network      At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person.Any questions? Feel free to email as at TalentAcquisition.de@abbvie.com – we look forward to hearing from you!Additional InformationAbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html

Senior Program Manager Technical Operations (all genders) - fulltime, permanent - AbbVie

&lt;strong&gt;Company Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;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 Twitter, Facebook, Instagram, YouTube and LinkedIn.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Looking for challenges where you can grow? We Offer That!&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Welcome to AbbVie! As part of an international company with 50,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity to work closely with us to address the health challenges of tomorrow. Do you have a passion for improving health care around the world and for using your expertise to improve patients' quality of life? In a challenging work environment that allows you to broaden and develop your own skills? You’ve found the right place!&lt;br&gt;&lt;br&gt;In our &lt;strong&gt;Tech Ops Department&lt;/strong&gt; at Ludwigshafen site, you will join a team of talented people and experienced experts in the manufacturing, packaging, engineering and global distribution of our approved and pipeline products – working with some of the most advanced technologies in the world.&lt;br&gt;&lt;br&gt;Develop your expertise and join our team as &lt;strong&gt;Senior Program Manager TO (all genders)&lt;/strong&gt; for global projects. You will be leading a cross-functional matrix team with integrity and respect, deliver results, champion change, foster collaboration, and teamwork, engage, and inspire.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Make an impact:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt; Develop project plans and timelines for new product introduction of innovative pipeline assets or tech transfers of established products - in alignment with the global strategy&lt;/li&gt;&lt;li&gt; Maintain operational awareness of the deliverables and upcoming needs to proactively identify, communicate and manage team risks, including escalation as appropriate with a strategic, cross-functional mindset&lt;/li&gt;&lt;li&gt; Ensure consistency and quality and financial compliance across all aspects of assigned programs&lt;/li&gt;&lt;li&gt; Develop business cases together with a cross-functional team and define recommendations that are specific and measurable&lt;/li&gt;&lt;li&gt; Routinely update cross-functional teams on status and changes as well as present Program updates and outcomes to executive management&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;This is how you can make a difference:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt; Technical background – Master of Science in Engineering, Chemistry or Pharmacy preferred&lt;/li&gt;&lt;li&gt; 8+ years of experience in positions related to process development, engineering/process support or manufacturing ideally in pharmaceutical packaging&lt;/li&gt;&lt;li&gt; 4+ years of experience in management of global projects and programs&lt;/li&gt;&lt;li&gt; Expertise in project management tools (e. g. Microsoft Excel, MS project and PowerPoint)&lt;/li&gt;&lt;li&gt; Strong GMP experience in pharmaceutical environment&lt;/li&gt;&lt;li&gt; Excellent verbal and written communication skills with demonstrated ability to communicate effectively to senior management&lt;/li&gt;&lt;li&gt; German and English both business fluent mandatory&lt;/li&gt;&lt;li&gt; Ability to develop and manage financial related elements of a project; strong business acumen including project and cost accounting&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Here's how we can grow together:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt; with a diverse work environment where you can have a real impact&lt;/li&gt;&lt;li&gt; with an open corporate culture&lt;/li&gt;&lt;li&gt; with an attractive salary&lt;/li&gt;&lt;li&gt; with an intensive onboarding process with a mentor at your side&lt;/li&gt;&lt;li&gt; with flexible work models for a healthy work-life balance&lt;/li&gt;&lt;li&gt; with a corporate health management that offers comprehensive health and exercise programs&lt;/li&gt;&lt;li&gt; with company social benefits&lt;/li&gt;&lt;li&gt; with a wide range of career opportunities in an international organization&lt;/li&gt;&lt;li&gt; with top-tier, attractive development opportunities&lt;/li&gt;&lt;li&gt; with a strong international network&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person.&lt;br&gt;&lt;br&gt;Any questions? Feel free to email as at TalentAcquisition.de@abbvie.com – we look forward to hearing from you!&lt;br&gt;&lt;br&gt;Additional Information&lt;br&gt;&lt;br&gt;AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:&lt;br&gt;&lt;br&gt;https://www.abbvie.com/join-us/reasonable-accommodations.html

Senior Program Manager Technical Operations (all genders) - fulltime, permanent

You need knowledge of global regulatory requirements, FDA Quality Systems, and strong communication skills. A Bachelor’s degree or 1-2 years of relevant experience is required.

You will ensure complaint records comply with global standards, document and investigate non-medical complaints, interface with stakeholders, and provide quality customer service for complaint resolution.

Healthcare

Austin

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 Individual will work in AbbVie’s global quality organization processing pharmaceutical, medical device and combination product complaints and inquiries. Interface with internal and external AbbVie customers such as physicians, nurses, pharmacists, hospital personnel, risk managers, purchasing agents, sales representatives, general public, manufacturing sites, technical support, commercial organization and PV regarding AbbVie product complaints. Responsible for product complaint documentation, investigations and identification of potential adverse events and potentially reportable events. Responsibilities * Assure complaint records meet global requirements. * Product complaint documentation, investigation, and review of all non-medical complaint content. Responsible for reviewing Medical complaints that involve a non-medical quality related event. * Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GCP. This requires good analytical skills, technical writing and good documentation. Responsible that complaint files meet all regulatory requirements. * Identification of potentially reportable events and notification to appropriate functional groups and management. * Interface with Third Party Manufacturers, health care professionals, general public, internal customers, AbbVie functional areas and regulatory agencies. * Provide quality customer service through coordination of return samples for investigation and follow up activities such as replacement of product, complaint categorization, and CAPA. Qualifications * Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination products. * Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and 211) is preferred. * Ability to prioritize multiple projects to ensure compliance with regulations and standard operating procedures is preferred. * Solid written/verbal communication and organizational skills. * Knowledge and application of computer systems for word processing and complaint management. * Ability to work with cross-functional teams and to interact effectively with peers, management, and customers. * A Bachelor's Degree required or 1-2 years of relevant work experience. Preferred degree in technology or scientific background (MLT, LPN, RN). * 0-2 years’ work experience in a cGMP related industry or in a clinical setting is preferred Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Company DescriptionAbbVie'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 DescriptionPurposeIndividual will work in AbbVie’s global quality organization processing pharmaceutical, medical device and combination product complaints and inquiries. Interface with internal and external AbbVie customers such as physicians, nurses, pharmacists, hospital personnel, risk managers, purchasing agents, sales representatives, general public, manufacturing sites, technical support, commercial organization and PV regarding AbbVie product complaints. Responsible for product complaint documentation, investigations and identification of potential adverse events and potentially reportable events.Responsibilities * Assure complaint records meet global requirements. * Product complaint documentation, investigation, and review of all non-medical complaint content. Responsible for reviewing Medical complaints that involve a non-medical quality related event. * Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GCP. This requires good analytical skills, technical writing and good documentation. Responsible that complaint files meet all regulatory requirements. * Identification of potentially reportable events and notification to appropriate functional groups and management. * Interface with Third Party Manufacturers, health care professionals, general public, internal customers, AbbVie functional areas and regulatory agencies. * Provide quality customer service through coordination of return samples for investigation and follow up activities such as replacement of product, complaint categorization, and CAPA.      Qualifications * Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination products. * Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and 211) is preferred. * Ability to prioritize multiple projects to ensure compliance with regulations and standard operating procedures is preferred. * Solid written/verbal communication and organizational skills. * Knowledge and application of computer systems for word processing and complaint management. * Ability to work with cross-functional teams and to interact effectively with peers, management, and customers. * A Bachelor's Degree required or 1-2 years of relevant work experience. Preferred degree in technology or scientific background (MLT, LPN, RN). * 0-2 years’ work experience in a cGMP related industry or in a clinical setting is preferred      Additional InformationApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs.      Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html

Complaint Analyst 1 - AbbVie

&lt;strong&gt;Company Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;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.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Job Description&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Purpose&lt;br&gt;&lt;br&gt;Individual will work in AbbVie’s global quality organization processing pharmaceutical, medical device and combination product complaints and inquiries. Interface with internal and external AbbVie customers such as physicians, nurses, pharmacists, hospital personnel, risk managers, purchasing agents, sales representatives, general public, manufacturing sites, technical support, commercial organization and PV regarding AbbVie product complaints. Responsible for product complaint documentation, investigations and identification of potential adverse events and potentially reportable events.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Assure complaint records meet global requirements.&lt;/li&gt;&lt;li&gt;Product complaint documentation, investigation, and review of all non-medical complaint content. Responsible for reviewing Medical complaints that involve a non-medical quality related event.&lt;/li&gt;&lt;li&gt;Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GCP. This requires good analytical skills, technical writing and good documentation. Responsible that complaint files meet all regulatory requirements.&lt;/li&gt;&lt;li&gt;Identification of potentially reportable events and notification to appropriate functional groups and management.&lt;/li&gt;&lt;li&gt;Interface with Third Party Manufacturers, health care professionals, general public, internal customers, AbbVie functional areas and regulatory agencies.&lt;/li&gt;&lt;li&gt;Provide quality customer service through coordination of return samples for investigation and follow up activities such as replacement of product, complaint categorization, and CAPA.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination products.&lt;/li&gt;&lt;li&gt;Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and 211) is preferred.&lt;/li&gt;&lt;li&gt;Ability to prioritize multiple projects to ensure compliance with regulations and standard operating procedures is preferred.&lt;/li&gt;&lt;li&gt;Solid written/verbal communication and organizational skills.&lt;/li&gt;&lt;li&gt;Knowledge and application of computer systems for word processing and complaint management.&lt;/li&gt;&lt;li&gt;Ability to work with cross-functional teams and to interact effectively with peers, management, and customers.&lt;/li&gt;&lt;li&gt;A Bachelor's Degree required or 1-2 years of relevant work experience. Preferred degree in technology or scientific background (MLT, LPN, RN).&lt;/li&gt;&lt;li&gt;0-2 years’ work experience in a cGMP related industry or in a clinical setting is preferred&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Additional Information&lt;br&gt;&lt;br&gt;Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. &lt;/li&gt;&lt;li&gt;We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. &lt;/li&gt;&lt;li&gt;This job is eligible to participate in our short-term incentive programs. &lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&lt;br&gt;&lt;br&gt;AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html&lt;br&gt;&lt;br&gt;US &amp;amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:&lt;br&gt;&lt;br&gt;https://www.abbvie.com/join-us/reasonable-accommodations.html

AbbVie

Mission