Senior Scientist, Bioanalysis
About The Position
The candidate for this Senior Scientist position will be working in the Regulated Bioanalysis group in the Quantitative, Translational, and ADME Sciences (QTAS) department. The primary responsibility will be acting as a Principal Investigator to manage projects and studies throughout the bioanalytical lifecycle, which includes but not limited to bioanalytical sample analysis, data review, and report writing for GLP non-clinical and clinical studies. The candidate must be experienced with managing bioanalytical operation workflows in a regulated environment. The individual will also be expected to work cross functionality within QTAS and with Preclinical Safety and Clinical Pharmacology.
Requirements
- Bachelor’s Degree and 10 years of experience OR Master’s Degree and 8 years of experience, OR PhD in Analytical Chemistry or related field required and no experience necessary.
- 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: 5500, 6500, 7500).
- 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.
- 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.
Nice To Haves
- Experience with Hamilton Starlet automated liquid handling instruments is a plus.
Responsibilities
- Overseeing 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 and approve method documents for regulated analysis and scientific papers for publication
- Expertise in the cutting-edge assay technologies and excellent assay troubleshooting skills
Benefits
- paid time off (vacation, holidays, sick)
- medical/dental/vision insurance
- 401(k)
- short-term incentive programs
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What This Job Offers
Job Type
Full-time
Career Level
Senior
