Senior Scientist II, Biologics Analytical R&D

AbbVie; North Chicago (IL); On-site; USD 106,000 - 203,000; Full time

Job summary

AbbVie is seeking a Senior Scientist II in Biologics Analytical R&D, focusing on developing advanced analytical techniques for the evaluation of biologics. The successful candidate will lead efforts in method development and contribute to regulatory submissions, working in a dynamic environment to address complex scientific challenges. Candidates should have a strong educational background with a focus on innovation in the field of pharmaceuticals.

Qualifications

• Ph.D. in Biochemistry, Analytical Chemistry, or a related discipline.
• Hands-on expertise with HPLC/UPLC and CE-SDS required.
• Proven record of creativity and scientific accomplishment.

Responsibilities

• Develop and optimize early-stage analytical methods.
• Collaborate with cross-functional teams on project readiness.
• Drive the development of automated workflows for liquid handling.

Skills

Analytical Method Development

Biophysics Techniques

Chromatography

Regulatory Strategy

Statistical Analysis

Project Management

Education

Ph.D. in Biochemistry

MS in Pharmaceutical Sciences

Tools

HPLC/UPLC

CE-SDS

Hamilton Liquid-handling Platforms

Tecan Liquid-handling Platforms

Job description

Senior Scientist II, Biologics Analytical R&D

Join to apply for the Senior Scientist II, Biologics Analytical R&D role at AbbVie

Senior Scientist II, Biologics Analytical R&D

Join to apply for the Senior Scientist II, Biologics Analytical R&D role at AbbVie

This range is provided by AbbVie. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$106,500.00/yr - $202,500.00/yr

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 X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Group

AbbVie Biologics Analytical Research & Development (Biologics Analytical R&D) is a global analytical sciences organization responsible for all CMC analytical activities related to the development of AbbVie's pharmaceutical products. Our Early Analytical Development team owns analytical strategy, method development, release & stability testing for IND-enabling biologic programs developed internally, partnering closely with Drug Substance, Drug Product, Regulatory Affairs, QA and Process Development Sciences & Technology.

Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologic medicines and spans from the selection of Discovery candidate molecules through the transition of analytical methods and testing to commercial labs to support product launch. We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines. Careers in AbbVie Biologics Analytical R&D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies.

The biologics early analytical development group develops state-of-the-art analytical techniques for analysis of therapeutic proteins and other novel biologic molecules using separation science and other biophysical techniques. We are looking for diverse candidates with strong scientific and leadership experience to join the AbbVie Analytical R&D team and can offer exciting and rewarding career opportunities for these candidates.

Overview

The candidate will focus on development and implementation of analytical assays for the analysis of complex biologics including antibodies, antibody drug conjugates, and new modalities. The candidate will use and develop a variety of analytical techniques including chromatography, electrophoresis, spectroscopy, and automated methods. The successful candidate will contribute to the development and testing of complex and automated assays and will contribute to the continuous improvement and innovation within the group.

Key Responsibilities

• Effectively function as a scientist, generating original technical ideas and research or development strategies.
• Develop and optimize early-stage analytical methods using HPLC/UHPLC, CE-SDS and other separation/biophysical techniques.”
• Drive the development of automated workflows for liquid handling platforms to improve method robustness and throughput.
• Author CMC analytical sections of IND/IMPD filings and contribute to global regulatory strategy alongside Reg Affairs.
• Collaborate daily with DS, DP, QA, late-stage stakeholders, and external CROs to align on method readiness and data packages.
• Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.
• Independently responsible for project science within his/her area of expertise on one or more project teams leading the method development and validation for complex biologic therapeutics.
• Proactively seek out new information in the literature and incorporate this into individual projects as well as the overall program.
  
  

Qualifications

• Ph.D. degree in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences or a closely related discipline or MS degree with 8 years of experience.
• Qualification for Senior Scientist I: Ph.D. with 0-4 years of experience is required with relevant experience or MS with 8 years of experience.
• Qualification for Senior Scientist II: Ph.D. with 4+ years of experience is required with relevant experience or MS with 10 years of experience.
• Hands-on expertise with HPLC/UPLC and CE-SDS, plus working familiarity with Hamilton or Tecan liquid-handling platforms.
• Working knowledge of cGMP expectations for early clinical materials; routine QC execution is not expected.
• Experience applying chemometrics / multivariate data analysis (e.g., PCA, MVM) and statistics to model-based method development.
• Demonstrated record of independent thought, creativity and scientific accomplishment (e.g. peer reviewed journal publications, patents).
• Must have a solid understanding of protein/oligonucleotide chemistry and biochemistry, particularly as related to biologics drug development.
• Strong data and time organization/management skills coupled with strong interpersonal and effective communication skills for facilitating collaborations with a demonstrated ability to lead cross functional process development teams.
• Demonstrated scientific curiosity, creativity and comfort operating in ambiguity—key to inventing from scratch.
• Effective writer and communication of research or other regulatory materials.
• Experience with analytical Multivariate Analytical Procedures development and/or validation a plus.
  
  

Additional Information

• This is an on-site opportunity based in AbbVie's Abbott Park location in IL.
• Leveling will be commensurate to experience.
  
  

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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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