Senior Scientist I - Bioanalytics

AbbVie; North Chicago (IL); On-site; USD 97,000 - 184,000; Full time

Benefits offered by this job

Paid time off

Medical, dental, vision insurance

401(k) plan with company match

Short-term incentive programs

Job summary

AbbVie is seeking a Senior Scientist to lead the Regulated Bioanalysis group within QTAS. You will manage projects through bioanalytical lifecycle, review data, and author reports for GLP nonclinical and clinical studies.

The role requires expertise in LC-MS, regulatory bioanalysis, and cross-functional collaboration with Preclinical Safety and Clinical Pharmacology. Strong leadership and troubleshooting skills are essential.

Qualifications

• Ph.D. with zero years’ experience, M.S. with 8 years, or B.S. with 10+ years of pharma/CRO experience in Analytical Chemistry.
• Experience with regulated bioanalysis during drug development.
• Familiarity with ALCOA principles in regulated environments.

Responsibilities

• Oversee sample analysis in support of nonclinical and clinical trials.
• Manage internal/external stakeholders on deliverables and priorities.
• Stay updated on separations and mass spectrometry trends.

Skills

Bioanalysis

Regulated environment

Data review

Project management

Mass spectrometry

LC systems

Report writing

Team collaboration

Education

Ph.D.

M.S. in Analytical Chemistry or related

B.S. in Analytical Chemistry or related

Tools

AB Sciex triple quadrupole MS

WATSON LIMS

Analyst/Sciex OS

Shimadzu LC instruments

Hamilton Starlet

Job description

• Compensation: USD 96,500 - USD 183,500 - yearly

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

Job Description

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.

Key responsibilities include:

• 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

Qualifications

Qualifications

• Ph.D. with zero years’ experience, M.S. with 8 years, or B.S. with 10+ years of pharma or CRO experience and a degree in Analytical Chemistry or related field required.
• 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.
• 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.
• 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.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable 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.