Principal Research Scientist II, Analytical R&D
: Job Details :

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 DescriptionAbbVie Analytical Research & Development (Analytical R&D) is a global analytical scientific organization responsible for all CMC analytical activities related to the development of AbbVie's pharmaceutical products.  Our scope includes AbbVie's diverse pipeline of innovative small molecule medicines and spans from the selection of Discovery candidate molecules to Late Stage Clinical.  We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines.  Careers in AbbVie Analytical R&D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies.  We are looking for diverse candidates with strong scientific and leadership experience to join the AbbVie Analytical R&D team and can offer exciting and rewarding career opportunities for these candidates.Overview:For the Principal Research Scientist II position, we are seeking a highly motivated, experienced analytical scientist to lead a team of analytical scientists supporting early phase development of New Chemical Entities (NCEs) drug substance and drug product in both preclinical and clinical. The candidate should have extensive expertise in applying regulatory guidelines within an R&D environment with a fit for purpose mind set. The candidate will need experience in developing analytical control strategies, analytical method development, characterization, validation, release, and stability testing.He/she should be able to direct research and/or project activities along with professional development of a team by effectively mentoring, guiding and/or supervising scientific personnel. Should conceive, execute and communicate novel multi-disciplinary research or development strategies that achieve project and strategic goals. Serve as a lead scientist on projects and contribute scientific insights into multiple other projects or initiatives. Serve as a discipline expert and contact, drives functional performance by designing implementing studies aimed at new or improved products.He/she must foster productive collaborations within the global Analytical R&D organization and with R&D cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), and Quality Assurance (QA) and CMC-Regulatory. Responsibilities:+ Lead an analytical team of across a range of different experience levels to support the development of NCE candidates (RSM to API to DP) from pre-clinical through Phase II clinical trials.+ Mentor analysts on the development of phase-appropriate analytical strategies involving Drug Substance and Drug Product.+ Lead and mentor a team that demonstrates an industry leading function of testing and release of DS and DP for clinical and toxicological studies. Drive efficiency across his/her teams with a high-level of compliance.+ Collaborate across Analytical R&D and partner functions that improve the efficiency and effectiveness of the Analytical R&D organization and help position Analytical R&D as an industry leader relative to peer companies in terms of our science and product development capabilities.+ Encourage ideas and drive for continuous improvement and champion initiatives within Analytical R&D and across R&D partner functions.+ Understand and comply with AbbVie safety, quality and regulatory policies and government regulations.+ Raises the bar and is never satisfied with the status quo.+ Creates a learning environment, open to suggestions and experimentation for improvement.+ Being inclusive, collaborative, and builds a culture where everyone feels welcome and valued.Qualifications+ Bachelors, Masters, or Ph.D. in Analytical Chemistry typically with a minimum of 16 (BS), 14 (MS), or 8 (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.+ Demonstrate creative 'out of the box' thinking to solve difficult technical problems+ Champion new technologies to achieve project goals.+ Hands on experience with HPLC analysis and method development along with fundamental understanding and working knowledge of various analytical techniques including MS, GC, ICP-OES, IC, and NMR.+ 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.+ High-quality written and oral communication skills and ability to interact effectively with interdisciplinary scientists and engineers.+ Demonstrated leadership of technical teams and effective cross-functional communication+ Demonstrated capability to solve critical scientific and business problems+ Demonstrated ability to implement and to grow the capabilities of an analytical organization and develop scientists into future leadersAdditional InformationApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​+ ​This is an on-site role located at 222 Jacobs Street, Cambridge, MA (Legacy Cerevel Therapeutics location).+ 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. ​+ This job is eligible to participate in our long-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 & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: $133,500 - $253,500