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 Biologics Analytical R&D group in Irvine develops analytical capabilities for the development of neurotoxin biologics.
We are looking for a scientist with expertise both in bioassay development (cell-based bioassays and ELISAs) and digital automation (Power Query, Power Automate, coding in C++ / Python is a plus). The candidate must be proactive in identifying workflows that can be automated, results-driven to deliver improvements in the ways we work, and flexible to prioritization of bioassay testing as needed.
In addition to implementing digital automation solutions, the Scientist will collaborate on expanding the use of laboratory automation devices (Hamilton, Opentrons) and support the development and qualification of analytical methods for the analysis and characterization of neurotoxin and biologics entities.
He/She collaborates with scientific staffs to plan 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.
• Support development of phase appropriate separation methods to support toxin development programs
• 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.
• 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.
• 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.
• 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).
• 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.
Qualifications
Position will be hired based on level of experience:
• Scientist I – Bachelor’s Degree or equivalent education with typically 5 years of experience, or Master’s Degree or equivalent education with typically 2 years of experience.
• Scientist II – BS or equivalent education with typically 7 or more years of experience or MS or equivalent education with typically 5 or more years of experience.
• Experience with liquid handler systems (e.g. Hamilton, HighRes BioSolutions, Opentrons) and software is a plus
• Experience with Power Query, Power Automate, coding in Python and C++ is a plus
• Experience in the area of designing and qualifying in vitro cell-based assays to reflect the relevant molecular mode of action.
• Experience in cell culture and state-of-the-art cell and molecular
Location: United States
Posted: Sept. 23, 2024, 8:28 p.m.
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