Senior Scientist I, tLNP Formulation

BioSpace; North Chicago (IL); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k) plan

Job summary

A pharmaceutical company is seeking a Senior Scientist in North Chicago to lead initiatives in the development of targeted lipid nanoparticle assets. The successful candidate will design and execute formulation and process development activities, prioritize safety and quality, and collaborate across teams. A PhD in Pharmaceutics or related field is required, along with proven experience in formulation development. The company offers a comprehensive benefits package including medical and 401(k).

Qualifications

• PhD in Pharmaceutics, Chemical Engineering or Biotechnology required.
• Experience in formulation and process development for drug products.
• Ability to analyze multidisciplinary datasets effectively.

Responsibilities

• Lead formulation screening studies under stress conditions.
• Facilitate scale-up and technology transfer.
• Develop and communicate stability strategies for clinical-stage programs.

Skills

Formulation development

Process development

Statistical analysis

Communication skills

Education

PhD in Pharmaceutics or related field

Tools

Dynamic Light Scattering (DLS)

Differential Scanning Calorimetry (DSC)

RP-HPLC

Job description

Overview

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

About the Team
The Targeted Lipid Nanoparticle (tLNP) drug product development group within AbbVie’s tLNP CMC team is committed to advancing clinical-stage tLNP assets from First-in-Human (FIH) through Phase 2. The team collaborates across biologics discovery, CMC partners, Clinical Operations, Regulatory Affairs, Quality Assurance, and external manufacturing to support development and commercialization of tLNP products. Key focus areas include establishing robust formulation and process development capabilities, leading critical CMC activities for pipeline programs, devising formulation development strategies, conducting stability evaluations, optimizing clinical in-use strategies, developing innovative product presentations, implementing stage-based quality risk management, and driving scientific initiatives to ensure the strong development of current and future tLNP programs.

Purpose

We are seeking a Senior Scientist to lead key scientific initiatives and provide leadership in the development of early stage targeted Lipid Nanoparticle (tLNP) assets within AbbVie’s pipeline. This role is responsible for designing, executing, and effectively communicating hypothesis-driven formulation and process development activities. The successful candidate will collaborate closely with analytical teams, process development groups, and subject matter experts across AbbVie to advance research and development in the tLNP space.

Responsibilities

• Assess tLNP liabilities under practical worst-case stress conditions to inform excipient selection and formulation screening strategies
• Design and execute comprehensive formulation screening studies, evaluating variables such as pH, buffer, antioxidants, surfactants, cryoprotectants, and other stabilizing excipients
• Lead process development, optimization, and robustness studies, with a focus on sterile fill-finish operations
• Facilitate scale-up, technology transfer, and manufacturing readiness in close collaboration with internal and external stakeholders
• Utilize statistical methods and Design of Experiments (DoE) to optimize formulations and process parameters
• Develop and communicate clinical in-use strategies for investigational products, including assessment of in-use stability for clinical-stage programs
• Plan and conduct experiments to evaluate innovative tLNP product presentations, such as lyophilized forms, spray-dried powders, nonaqueous suspensions, and other advanced formats
• Interpret and present critical data, key findings, and recommendations in both internal and cross-functional team forums
• Maintain high laboratory productivity while ensuring strict adherence to corporate safety, quality, and good research practices
• Practice robust documentation standards by accurately recording experimental data, results, and conclusions in electronic lab notebooks, technical reports, and scientific presentations

Qualifications

Required

• PhD in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, Biotechnology, or a related field (0+ years industry experience); or MS with 6+ years of relevant industry experience
• Comprehensive theoretical knowledge of ICH regulations governing drug product formulation and sterile process development
• Proven experience in formulation, process development, and analytical characterization of protein therapeutics
• Experience characterizing thermal (glass transition, recrystallization) and physico-chemical (pH shifts) events taking place at sub-zero temperatures (typically -20C to -80C) in frozen drug product solutions
• Proficient in formulation characterization methods such as Dynamic Light Scattering (DLS), Differential Scanning Calorimetry (DSC), and chromatographic techniques (RP-HPLC, SEC, IEX)
• Demonstrated ability to independently design, execute, and troubleshoot complex formulation experiments
• Skilled at analyzing and interpreting multidisciplinary datasets to enable scientific decision-making
• Exceptional written and verbal scientific communication skills

Preferred

• Hands-on experience in mRNA, lipid nanoparticles (LNP), targeted LNP systems, or biologics drug product development
• Demonstrated expertise in biologics manufacturing processes, including sterile fill-finish operations, lyophilization, and spray drying
• Strong familiarity with LNP and protein formulation characterization techniques such as mRNA encapsulation efficiency assays and antibody binding assays (qELISA)
• Proficient in utilizing statistical software and Design of Experiments (DoE) methodologies for process and formulation optimization.

Additional Information

• 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.

AbbV ie 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, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

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