<h3>Job Description</h3><div>Job Description<div>Company Description At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit https://global.allerganaesthetics.com/. Follow Allergan Aesthetics on LinkedIn.Job Description Position Summary:Principal Research Scientist I (Team Lead) will be leading a group of scientists and drive protein delivery and formulation innovation to enable next generation of medical aesthetic products. The ideal candidate has a track record in developing innovative protein delivery technologies (e.g. solutions, particles or gels) to achieve clinically differentiating product profiles, has deep understandings of fundamental drug delivery sciences, is experienced with early pharmaceutical development and CMC practices for protein formulation products and is highly effective in driving collaborations in a complex corporate matrix. Knowledge of biopolymers as well as biochemical or biophysical characterization of proteins is a plus. Communication and leadership skills as required for cross-functional collaborations and people management are essential.Key Duties / Responsibilities:Scientific Leadership 20%<ul><li>Leads a technical team to advance a technology platform or a product.</li><li>Represents Biomaterials & Drug Delivery to provide technical leadership for research and development programs.</li><li>Represents Abbvie and provides leadership on external collaborations.</li><li>Steers the assessment of future delivery technologies according to pipeline needs; identifies internal as well as external technology opportunities and champions critical scientific assessment</li><li>Serves as a technical advisor and subject matter expert to the company’s business. Actively contributes to the company’s patent portfolio through continuous innovation.</li></ul>Scientific Execution 40%  <ul><li>Develops detailed project plans including scientific approaches and realistic deliverables with budgets and timelines.</li><li>Executes studies to develop a formulation or drug delivery technology.</li><li>Designs and develops analytical tools to characterize the formulation including drug interaction with excipients.</li><li>Aligns cross-functionally and executes study plans to advance a drug product through Discovery and early Development stages.</li><li>Organizes, leads, and/or participates in project team meetings to define and schedule project activities and review completed tasks.  </li><li>Writes, reviews and issues technical reports, technical memoranda, and other documents for internal and external distribution.</li></ul>Scientific Communication 25%<ul><li>Communicates project status to project team leaders, functional managers, and R&D committees as appropriate. Drives alignment with cross-functional teams and management for activities and deliverables.</li><li>Represent the Biomaterials & Drug Delivery to interface with cross functional management and internal customers. Remains as an internal subject matter expert through the entire product development life cycle.</li><li>Generates ROI’s and works closely with corporate patent counsel in generating IP documentation.</li></ul>External Scientific Interaction 10%<ul><li>Searches, reviews, and evaluates current technology landscape to maintain and extend internal technical competence.</li><li>Attends and participates in scientific meetings as company’s representative to gain knowledge about new products or technologies pertinent to corporate business interest.</li><li>Communicates and recommends new biomaterial, product, and technology related ideas to supervisor and other research managers to maintain and enhance company’s position in the marketplace.</li></ul>Talent Management 5%<ul><li>Manages/trains/mentors junior staff as direct reports or as part of a project team in a matrix-based organization.</li><li>Participates in identifying, interviewing, and hiring new talents.</li><li>Manages day to day performance of direct reports, as needed. </li></ul>Qualifications Minimum Requirements:<ul><li>Ph.D. or M.S.-level education in Biomaterials Science, Polymer Chemistry, Bioengineering, Chemical Engineering, Biochemistry, Pharmaceutical Sciences, Drug Delivery Sciences, or related fields.</li><li>6+ (Ph.D.), 12+ (M.S.) or 14+ (B.S.) years of applicable experience including industrial experience is required.</li><li>Work experience involving biomaterials for drug delivery systems and medical device and is preferred.</li></ul>Essential Skills & Abilities:Leadership/ Management  <ul><li>Ability to lead scientific innovations and translate them into new product concepts and opportunities</li><li>Ability to create scientific ideas and define research approaches to drive project deliverables within timelines</li><li>Ability to effectively present information and respond to questions from groups of managers or technical peers.</li><li>Ability to present facts and recommendations effectively in both oral and written form. </li><li>Ability to interface with multiple levels of employees at various disciplines within various departments</li><li>Ability to work/manage cross-functional teams</li><li>Ability to lead and mentor junior staff or serve as a senior technical advisor</li></ul>Technical<ul><li>Possess high degree of technical competence and expertise in Biomaterials Science (e.g., polymer synthesis, cross-linked/modified polymers, hydrogels, biodegradable polymers or vehicles, biomaterial-tissue interfaces, polymer fabrication processes, drug delivery systems, and tissue scaffolding/engineering)</li><li>Demonstrate critical thinking and problem-solving skills and excellent communication skills, both oral and written. </li><li>Working knowledge of general laboratory techniques and procedures including EHS practice. </li><li>Ability to accurately perform detail-oriented work.</li><li>Ability to prioritize and manage concurrent projects</li><li>Ability to maintain accuracy, consistency and quality of documentation while adhering to company deadlines.</li><li>Ability to learn and function in a controlled environment regulated by FDA GMPs and handle confidential data, as needed.</li><li>Ability to read, analyze, and interpret general business periodicals, professional journals, technical journals and procedures and governmental regulations.</li><li>Ability to write reports, business correspondence, documentation and procedures.</li><li>Ability to interact and negotiate successfully with suppliers and vendors.</li><li>Ability to take initiative and make decisions within own work content</li><li>Ability to use word processing, spreadsheet and database applications.</li><li>Ability to learn various software programs</li></ul> Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​<ul><li>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.​</li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​</li><li>This job is eligible to participate in our short-term incentive programs. ​</li></ul><ul><li>This job is eligible to participate in our long-term incentive programs. ​</li></ul> 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. ​<div></div>AbbVie 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.</div></div>

<h3>Job Description</h3><div>Job Description<div>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 Envision working with energetic colleagues and inspirational leaders. Now, place yourself in that mix; leading discussions, asking the right questions, and driving results. The Principal Research Scientist is responsible for supporting the development, qualification, transfer and validation of analytical methods for the analysis and characterization of neurotoxin and biologics entities.He/She independently plans experimental work and executes protocols in support of biologics process development, formulation development, and stability studies. The individual independently generates, compiles, and evaluates data for technical reports to support regulatory filings for new and currently marketed biological products. The individual is also responsible for writing sections or subsections of technical reports, method and/or operational SOPs. He/She independently carries out multiple analytical methods to support AbbVie biologics projects depending on departmental needs. Maintains a productive and collaborative laboratory environment consistent with regulatory and company expectations.The position requires the individual to work with and in areas requiring select agents and toxins access (i.e. Biosafety level 2 laboratories). Access to and use of select agents is regulated by federal policies. Therefore, the candidate must conduct all work activities in compliance with AbbVie internal and applicable regulatory requirements. AbbVie internal requirements include compliance with ethics, environmental health and safety, financial, human resources, and general business policies, requirements and objectives.Key Responsibilities  <ul> <li>Lead development of phase appropriate separation methods to support toxin development programs at various phases by managing direct reports</li> <li>Execute the development and validation of analytical methods for the analysis and characterization of biopharmaceuticals. Create written procedures and protocols. Transfer, qualify or validate methods as needed.</li> <li>Represent department for important organization-wide initiatives to support establishment of infrastructures</li> <li>Apply routine and specialized analytical techniques to characterize and quantify biopharmaceuticals. Maintain reagent supplies, notebooks, summarizes results in written reports and communicates observations to ensure that the end user receives quality methods in a timely manner. Comply with Quality Principals related to data generation and reporting.</li> <li>Actively participate on cross-functional teams within Biologics Development and provide support to external departments. Openly share scientific expertise and collaboratively help the team to formulate rational solutions to problems.</li> <li>Develop protocols and SOPs, train staff and maintain the laboratory consistent with departmental and company requirements. Understand, document, and adjust Quality Systems to match the project stage (e.g. pre-development or development).</li> <li>Maintain a good and current knowledge of the scientific and technical literature pertinent to the project and necessary for development of state-of-the-art analytical methods, including the acquisition of necessary equipment.</li> <li>Keep up-to-date on current and cutting-edge developments in the biologics characterization field.</li> <li>Make high quality scientific presentations at internal management, regional and national meetings to help advance AbbVie’s image as the thought and product leader in the neuromodulator field. Present and defends product, assay and process data to regulatory agencies.</li> <li>Make staffing recommendations related to direct reports and communicates desired forward path to mid-and-senior level management for endorsement/implementation. Evaluates performance for direct reports and assists with staff development via recommendations for internal and external technical training and scientific conferences. Consistently treats direct reports and other team members and all Abbvie employees with respect</li> <li> </li></ul>Qualifications <ul><li>BS or equivalent education and extensive, typically 14+ years of experience; MS or equivalent education with typically 12+ years of experience; PhD with typically 6+ years of experience in area or scientific area of discipline.</li><li>Advanced knowledge and experience in developing, validating and transferring separation methods for biologics, including HPLC (RP, SEC,  HIC, IEX), gel and capillary electrophoresis (SDS-PAGE, native-PAGE, CE, cIEF)</li><li> A strong analytical and instrument skills and a thorough understanding and working knowledge of analytical method development and validation.</li><li> A solid understanding of methods and procedures related to the production and characterization of biopharmaceuticals in a regulated environment is expected.</li><li>Extensive working knowledge of the requirements of working in a cGMP/GSP environment is desired.</li><li>Prior experience of supervising staffs is highly desired</li><li>Thorough understanding in CMC development strategy of biologics drugs is expected.</li></ul>  Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​​<ul><li>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.​</li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​</li><li>This job is eligible to participate in our short-term incentive programs. ​</li><li>This job is eligible to participate in our long-term incentive programs​</li></ul>​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. <div></div>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 </div></div>

Research Scientist - Deep Learning We are currently partnered with an AI-driven Security startup (based near Irvine) who use AI & Deep Learning to transform the way in which digital assets are protected and safeguarded. They are looking to bring a Senior Research Scientist into the team to work alongside their existing ML Scientists & Engineers. The current team consists of ex-Microsoft & Amazon researchers who work at the intersection of complex, uncharted AI & Security research, and the position would see you leading streams of Deep Learning Research and publishing in top-tier conferences and journals. The position would have both an Applied and Theoretical focus, meaning your work would have a tangible impact on the roadmap for their product and the innovation behind it. We are looking for individuals with: -> PhD in Machine Learning, Computer Science, Computer Vision or a related field-> Publications in top-tier conferences & journals - NeurIPS / ICCV / ICLR etc-> Strong Deep Learning Research experience This is a great chance to join a startup with customers, significant traction, features in TechCrunch, Forbes and more and who are working on a brand new problem area. Please apply ASAP for more detail.

Research Scientist Jobs in Irvine, CA

Principal Research Scientist I Biomaterials Drug Delivery
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July 26, 2024

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Principal Research Scientist I Biomaterials Drug Delivery
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Director Biological Researchsenior Principal Research Scientist
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Principal Research Scientist Ii Biomaterials Drug Delivery
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Research Scientist Deep Learning
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Research Scientist Jobs in Irvine, CA

Principal Research Scientist I Biomaterials Drug DeliveryJuly 26, 2024

Principal Research Scientist I Biologics Analytical Rd SeparationJuly 26, 2024

Principal Research Scientist I Biologics Analytical RdJuly 16, 2024

Principal Research Scientist I Biomaterials Drug DeliveryJuly 8, 2024

Director Biological Researchsenior Principal Research ScientistJuly 8, 2024

Principal Research Scientist Ii Biomaterials Drug DeliveryJuly 8, 2024

Research Scientist Deep LearningJune 30, 2024