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 (https://www.tiktok.com/@abbvie) . Job Description The Product Development Science and Technology (PDS&T) Analytical group is currently seeking a Senior Scientist I to join our team. As a Senior Scientist I, you will have the opportunity to independently design and execute analytical methods to support robust manufacturing processes development for clinical phase and commercial products. You will play a crucial role in ensuring the quality and efficacy of our products, making a direct impact on patient health and well-being. This position involves highly collaborative work where you will have the chance to work closely with cross-functional teams including process and product development, CMC, process engineering, internal and external manufacturing, quality assurance, supply chain, and Operations Manufacturing Sites. This collaborative environment will allow you to expand your knowledge and skills while making meaningful contributions to our organization. Further you will be a part of the effort to build automated analytical workflows and deriving insights from large data sets deploying advanced statistical approaches aligned with our fit for the future principles. Responsibilities: + Responsible for leading the analytical aspects of a project while working with other functional areas to advance projects through the development pipeline. + Apply analytical separation and detection modes for complex impurity profiling of pharmaceutical products to further the understanding of emerging cGMP manufacturing processes. + Utilize understanding of a range of analytical techniques to conduct research and development studies related to small-molecule drug products, active pharmaceutical ingredients, intermediates, starting materials, impurities and impurity profiling. + Develop and leverage automated/real-time analysis approach as alternative to manual approaches and apply novel data analysis to large data sets to derive insights to support Lab/Factory of the Future effort + Support new product development with advanced methods development and validations, technical transfer packages, and generation of technical data in support regulatory requirements. + Highly autonomous and productive in performing laboratory research or method development, requiring only minimal direction from or interaction with supervisor. + Formulate conclusions and design follow-on experiments based on multidisciplinary data. + May initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a development program. + Process, interpret, and visualize data to facilitate project team decisions. + Communicate and collaborate with cross-functional groups and departments. + Routinely demonstrate scientific initiative and creativity in development activities and maintain a high level of productivity in the lab. + Responsible for method development, testing procedures, and implementation of analytical control strategies to help the advancement of pipeline candidates. + Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, and GxP compliance, where applicable. Qualifications + Bachelors, Masters, or Ph.D. in Analytical Chemistry, or Physical Chemistry typically with 10 to 12 (BS), 8 to 10 (MS), or 0 to 4 (Ph.D.) years related industry experience. + Strong technical background in analytical chemistry, excellent analytical problem-solving skills. Capable of independently developing and troubleshoot analytical methods. + Hands on experience with HPLC analysis and method development along with expertise and fundamental understanding of spectroscopic techniques. + Self-motivated, hard-working, detail-oriented individual able to work in a fast-paced team environment. + Experience in the use of computerized data handling systems, data analysis and statistical approaches + High-quality written and oral communication skills and ability to interact effectively with interdisciplinary scientists and engineers. Preferred: + Advanced degree in Analytical/Physical Chemistry. + Understanding of cGMP and current regulatory requirements. + Practical knowledge of organic structure, functional groups, chemistry, and modern spectroscopic techniques as applied to small-molecule analytical analysis. Key Leadership Competencies: + Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance. + Learns fast, grasps the "essence" and can change course quickly where indicated. + Raises the bar and is never satisfied with the status quo. + Creates a learning environment, open to suggestions and experimentation for improvement. + Embraces the ideas of others, nurtures innovation and manages innovation to reality. 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. All your information will be kept confidential according to EEO guidelines. 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 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 Salary: $35,000 - $172,500