Sr Scientist II, Pharmacology
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Job Location:
North Chicago, IL - USA
Monthly Salary:
Not Disclosed
Posted on:
23 days ago
Vacancies:
1 Vacancy
Job Summary
The Senior Scientist II position will be working in the Regulated Bioanalysis group in the Quantitative Translational and ADME Sciences (QTAS) department. The primary responsibility will be to manage projects throughout the bioanalytical lifecycle including bioanalytical sample analysis data review and report writing for GLP non-clinical through clinical studies. The Senior Scientist II must be experienced in developing and validating LC-MS based methods in a regulated environment. The individual will also be expected to work cross functionality within QTAS and with Preclinical Safety and Clinical Pharmacology.
Key responsibilities include:
- Overseeing method development validation and sample analysis of Abbvie assets in support of nonclinical and clinical trials according to regulatory requirements.
- Managing internal and external stakeholders on deliverables and priorities
- Maintain awareness of evolving trends in separations and mass spectrometry
- Maintain and troubleshoot complex LC systems and ultra-sensitive mass spectrometers
- Author method documents for regulated analysis and scientific papers for publication
- Expertise in the cutting-edge assay technologies and excellent assay troubleshooting skills
Key Leadership Competencies:
- Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance.
- Learns fast grasps the essence and can change course quickly where indicated.
- Raises the bar and is never satisfied with the status quo.
- Creates a learning environment open to suggestions and experimentation for improvement.
- Embraces the ideas of others nurtures innovation and manages innovation to reality.
Qualifications :
Qualifications
- Bachelors Degree and typically 12 years of experience Masters Degree and typically 10 years of experience PhD and typically 4 years of experience.
- Experience with regulated bioanalysis support in the drug development process.
- Experience with regulatory guidelines for bioanalysis and experience working in a regulated environment (ALCOA principles).
- Experience developing and validating bioanalytical methods for small molecules large molecules and peptides.
- Experience with operating AB Sciex triple quadrupole mass spectrometers or equivalents (ex:).
- Experience with electronic laboratory notebook software WATSON Laboratory Information Management Software (LIMS) and AB Sciex Analyst/Sciex OS Software.
- Experience with operating Shimadzu Liquid Chromatography instruments or equivalents.
- Experience with Hamilton Starlet automated liquid handling instruments is a plus.
- Strong interpersonal skills the ability to work independently with minimal supervision in managing multiple projects and priorities and work well within a team and a desire to learn specific techniques for bioanalysis.
Additional Information :
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
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 Companys sole and absolute discretion unless and until paid and may be modified at the Companys 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.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Key Skills
- Laboratory Experience
- Immunoassays
- Machine Learning
- Biochemistry
- Assays
- Research Experience
- Spectroscopy
- Research & Development
- cGMP
- Cell Culture
- Molecular Biology
- Data Analysis Skills
About Company
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more
