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Pharmaceutical Formulation Development Jobs in Chicago, IL

Freseniusglobal

Sr Project Engineer

Melrose Park, IL

$96K - $126K/yr

... development of new/alternative complex formulation and processing technologies for the improvement of current commercial projects for parenteral nutrition and generic pharmaceuticals. Salary Range ...

Fresenius Kabi

Sr Project Engineer

Melrose Park, IL · On-site

$96K - $126K/yr

... development of new/alternative complex formulation and processing technologies for the improvement of current commercial projects for parenteral nutrition and generic pharmaceuticals. Salary Range ...

Frontage Laboratories

Analytical Chemist

Chicago, IL · On-site

$65K - $80K/yr

Prepare and review Method Development/Validation and Dose Formulation Analysis (DFA) reports for ... Pharmaceutical Sciences, or related field. * Hands-on experience with HPLC and UPLC systems.

Tekni-Plex

Development Engineer I

Schaumburg, IL · On-site

... pharmaceutical, food & beverage, beauty, and personal care. Here, your ideas count and your work ... formulation technologies, key internal processes, and customer processes. * The Product Development ...

Tekni-Plex

Development Engineer I

Schaumburg, IL · On-site

... pharmaceutical, food & beverage, beauty, and personal care. Here, your ideas count and your work ... formulation technologies, key internal processes, and customer processes. * The Product Development ...

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Pharmaceutical Formulation Development information

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How much do pharmaceutical formulation development jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for pharmaceutical formulation development in Chicago, IL is $52.42, according to ZipRecruiter salary data. Most workers in this role earn between $35.67 and $83.94 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in pharmaceutical formulation development?

To thrive in Pharmaceutical Formulation Development, you generally need a strong background in pharmaceutical sciences, chemistry, or related fields, and experience with drug formulation principles and analytical techniques. Familiarity with laboratory instrumentation (such as HPLC, dissolution testers), regulatory documentation systems, and GMP/GLP compliance is essential. Excellent problem-solving abilities, attention to detail, and cross-functional communication skills help you excel in a team-oriented environment. These competencies ensure the creation of safe, effective, and commercially viable pharmaceutical products that meet regulatory standards.

What are the main responsibilities of someone working in pharmaceutical formulation development?

Professionals in Pharmaceutical Formulation Development are typically responsible for designing and optimizing drug formulations, conducting laboratory experiments, and ensuring products meet safety, efficacy, and stability standards. Their work often involves collaborating closely with analytical, manufacturing, and regulatory teams to advance products from early development to commercial scale-up. They may also troubleshoot formulation issues, document experimental results, and contribute to regulatory submissions. The role requires careful attention to detail, a strong scientific foundation, and the ability to work both independently and as part of a multidisciplinary team.

What is pharmaceutical formulation development?

A Pharmaceutical Formulation Development job involves designing and optimizing drug formulations to ensure safety, efficacy, and stability. Professionals in this role work on selecting appropriate excipients, determining dosage forms, and improving drug delivery methods. They collaborate with regulatory teams to meet compliance standards and conduct tests to assess product performance. This role is essential for bringing new medications from the research phase to commercial production.

What are the most commonly searched types of Pharmaceutical Formulation Development jobs in Chicago, IL? The most popular types of Pharmaceutical Formulation Development jobs in Chicago, IL are:
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Pharmaceutical Formulation Development jobs near you
Infographic showing various Pharmaceutical Formulation Development job openings in Chicago, IL as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $109,040 per year, or $52.4 per hour.

Senior Scientist I / II - Biologics Analytical R&D

AbbVie

North Chicago, IL • On-site

$109K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 days ago

AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 100 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

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
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 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.
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.
  • 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.
  • Work in partnership with colleagues from Discovery, Process Chemistry/Engineering Formulation Development, and Characterization departments, among others.

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.
  • Practical experience and strong knowledge in one or more of the following areas: protein/oligonucleotide HPLC, capillary electrophoresis, MALS, automation and/or spectroscopy for biologics.
  • Previous cGMP or GLP experience and attention to detail in documentation.
  • 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.
  • Effective writer and communication of research or other regulatory materials.
  • Experience with analytical Multivariate Analytical Procedures development and/or validation a plus.

Leveling will be commensurate to experience.
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.

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.
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

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines 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, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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