AbbVie
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Senior Scientist, II
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AbbVie This range is provided by AbbVie. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$106,500.00/yr - $202,500.00/yr 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. Job Description AbbVie Parenteral Product Development Science & Technology (PDS&T) is a global organization responsible for all CMC activities related to the development and commercialization of AbbVie's parenteral products. Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologics medicines, including monoclonal antibodies, antibody drug conjugates (ADC), and other novel modalities, and spans from clinical proof of concept through commercial product launch. The Analytical Development group within Parenteral PDS&T is responsible for biologics programs that are transitioning from development stage to optimization and commercialization. We lead final method development, optimization, and validation, ensuring all analytical methods are fit for use in commercial QC laboratories. Key Responsibilities: Routinely demonstrate scientific initiative and creativity in research and development activities to solve difficult problems and champion new analytical technologies to achieve project goals. Perform method development, optimization, and validation for late-stage biologics programs. Independently responsible for project activities within area of expertise while also contributing within the project team to the overall progress of the program. Deliver results in a team-oriented setting and willing to work across scientific disciplines to drive programs through critical milestones. Generate new scientific proposals and lead those efforts. Anticipate and critically evaluate scientific or regulatory advances or competitive threats and respond with appropriate new strategies. Effectively organize and present scientific plans and data. Author technical documents (e.g., methods, protocols, reports, etc.), scientific publications, presentations, and regulatory documents. Qualifications PhD (4+ years), Master’s Degree (10+ years), or Bachelor’s Degree (12+ years) in scientific discipline (e.g., Analytical Chemistry, Biochemistry, or Biology) with previous laboratory experience. Practical experience with method validation and working in a GMP environment is required. Practical experience and strong knowledge of protein HPLC (e.g., SEC, IEX, HIC), capillary electrophoresis (e.g., icIEF, CE-SDS), and other separation techniques as applied to protein analysis is preferred. Solid understanding of protein chemistry and biochemistry, particularly as related to biologics drug development, is preferred. Maintain a laboratory notebook in compliance with Good Laboratory/Manufacturing Practices. Demonstrated independent problem-solving ability in science and technical proficiency. Demonstrated ability to learn, understand, and master new experimental techniques. Ability to multitask and work within timelines. Demonstrated scientific writing skills and strong verbal communication skills. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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Senior Scientist, II
role at
AbbVie This range is provided by AbbVie. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$106,500.00/yr - $202,500.00/yr 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. Job Description AbbVie Parenteral Product Development Science & Technology (PDS&T) is a global organization responsible for all CMC activities related to the development and commercialization of AbbVie's parenteral products. Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologics medicines, including monoclonal antibodies, antibody drug conjugates (ADC), and other novel modalities, and spans from clinical proof of concept through commercial product launch. The Analytical Development group within Parenteral PDS&T is responsible for biologics programs that are transitioning from development stage to optimization and commercialization. We lead final method development, optimization, and validation, ensuring all analytical methods are fit for use in commercial QC laboratories. Key Responsibilities: Routinely demonstrate scientific initiative and creativity in research and development activities to solve difficult problems and champion new analytical technologies to achieve project goals. Perform method development, optimization, and validation for late-stage biologics programs. Independently responsible for project activities within area of expertise while also contributing within the project team to the overall progress of the program. Deliver results in a team-oriented setting and willing to work across scientific disciplines to drive programs through critical milestones. Generate new scientific proposals and lead those efforts. Anticipate and critically evaluate scientific or regulatory advances or competitive threats and respond with appropriate new strategies. Effectively organize and present scientific plans and data. Author technical documents (e.g., methods, protocols, reports, etc.), scientific publications, presentations, and regulatory documents. Qualifications PhD (4+ years), Master’s Degree (10+ years), or Bachelor’s Degree (12+ years) in scientific discipline (e.g., Analytical Chemistry, Biochemistry, or Biology) with previous laboratory experience. Practical experience with method validation and working in a GMP environment is required. Practical experience and strong knowledge of protein HPLC (e.g., SEC, IEX, HIC), capillary electrophoresis (e.g., icIEF, CE-SDS), and other separation techniques as applied to protein analysis is preferred. Solid understanding of protein chemistry and biochemistry, particularly as related to biologics drug development, is preferred. Maintain a laboratory notebook in compliance with Good Laboratory/Manufacturing Practices. Demonstrated independent problem-solving ability in science and technical proficiency. Demonstrated ability to learn, understand, and master new experimental techniques. Ability to multitask and work within timelines. Demonstrated scientific writing skills and strong verbal communication skills. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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