Serve as a technical expert responsible for independently investigating, identifying, developing, and optimizing innovative methods and techniques to address critical project objectives. Proactively drive continuous improvement of existing laboratory processes and methodologies. Critically review and apply relevant scientific literature to fulfill project assignments. Demonstrate comprehensive expertise across a broad range of experimental techniques and data analysis methods.
Independently design, execute and interpret critical experiments to answer scientific questions. Understand the broad objectives of the project as well as their role in achieving those objectives, and modify experimental plan when required, to respond. Learn, understand and master new experimental techniques, and act as a resource or mentor for others. Innovate and implement new experimental protocols. Demonstrate a high level of proficiency in his/her field. Set and meet experimental timelines. Effectively organize and present scientific plans and data. Contribute to writing and conceptual framework of publications, presentations, and patents. Routinely read and apply relevant scientific literature. Impact projects mostly through lab and/or pilot plant based activities where applicable.
BS, preferably in Chemical Engineering or equivalent education with typically 7 or more years of experience or MS or equivalent education with typically 5 or more years of experience. Demonstrated ability to independently design, execute and interpret critical experiments to answer scientific questions. 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.
Possess thorough theoretical and practical understanding of own scientific discipline. Experience in the Medical Device field. Experience with biomaterial devices. Experience in working with cross functional teams. Experience with hydrogels. Experience in Process Development and/or Process Validation.
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. 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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Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.
Tagged as: Life Sciences
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