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Formulation Development Cmc Jobs in Chicago, IL (NOW HIRING)

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Formulation Development Cmc information

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How much do formulation development cmc jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for formulation development cmc 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 is the role of CMC in drug development?

In formulation development, CMC (Chemistry, Manufacturing, and Controls) ensures the quality, safety, and efficacy of a drug by establishing manufacturing processes, quality standards, and regulatory documentation. Formulation scientists and CMC teams collaborate to develop stable, scalable drug products that meet regulatory requirements throughout development and commercialization.

What is the salary of formulation R&D?

The salary for a Formulation Development CMC professional typically ranges from $70,000 to $130,000 annually, depending on experience, education, and location. Entry-level roles may start lower, while senior positions with specialized skills or certifications can earn higher salaries. Compensation often includes benefits such as health insurance and bonuses.

What is the highest paying job in pharmaceuticals?

In pharmaceuticals, senior roles such as Vice President of Research and Development or Chief Scientific Officer typically have the highest salaries, often exceeding several hundred thousand dollars annually. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee drug development, regulatory strategies, and company innovation.

What is the difference between Formulation Development Cmc vs Formulation Scientist?

AspectFormulation Development CmcFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fields; industry certificationsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields
Work EnvironmentPharmaceutical or biotech R&D labs, manufacturing settingsResearch labs, development facilities, pharmaceutical companies
Industry UsageRegulatory submissions, product development, manufacturing supportFormulation research, experimental design, product optimization

Formulation Development Cmc focuses on developing formulations suitable for regulatory approval and manufacturing, often involving documentation and compliance. Formulation Scientists primarily conduct research and experiments to create and optimize formulations. While both roles require similar educational backgrounds and work in related environments, Cmc roles emphasize regulatory and manufacturing aspects, whereas Scientists focus on experimental research and innovation.

Is formulation part of CMC?

In formulation development roles within CMC (Chemistry, Manufacturing, and Controls), formulation is a core component, involving the design and optimization of drug formulations to ensure stability, efficacy, and manufacturability. These professionals work with analytical tools, quality standards, and regulatory requirements to develop suitable formulations for clinical and commercial products.

What is Formulation Development CMC?

Formulation Development CMC (Chemistry, Manufacturing, and Controls) refers to the process of designing and optimizing the composition of a drug product, ensuring it is safe, effective, and stable for patient use. This role involves selecting appropriate excipients, developing the manufacturing process, and generating the data required to support regulatory submissions. CMC professionals collaborate with research, quality, and regulatory teams to ensure that the drug product meets all necessary standards throughout its lifecycle.

What are the key skills and qualifications needed to thrive as a Formulation Development CMC specialist, and why are they important?

To thrive as a Formulation Development CMC specialist, you need expertise in pharmaceutical sciences, chemistry, and regulatory guidelines, often supported by an advanced degree in a relevant field. Familiarity with analytical techniques, formulation equipment, and regulatory submission systems like eCTD is crucial. Strong problem-solving skills, attention to detail, and effective collaboration are essential soft skills in this role. These competencies ensure the successful development, optimization, and regulatory approval of safe and effective pharmaceutical products.

What are some typical challenges faced by professionals in Formulation Development CMC, and how are they addressed?

Professionals in Formulation Development CMC often encounter challenges such as ensuring formulation stability, meeting regulatory requirements, and scaling up from laboratory to manufacturing. Addressing these challenges requires close collaboration with analytical, regulatory, and manufacturing teams, as well as staying current with evolving guidelines. Effective project management, rigorous experimental design, and proactive risk assessment are key strategies to successfully navigate these complexities and ensure timely progress of drug development projects.
What job categories do people searching Formulation Development Cmc jobs in Chicago, IL look for? The top searched job categories for Formulation Development Cmc jobs in Chicago, IL are:
What cities near Chicago, IL are hiring for Formulation Development Cmc jobs? Cities near Chicago, IL with the most Formulation Development Cmc job openings:
Associate Scientist I, Solid State/Material Science

Associate Scientist I, Solid State/Material Science

AbbVie

North Chicago, IL • On-site

$58K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


AbbVie rating

8.6

Company rating: 8.6 out of 10

Based on 98 frontline employees who took The Breakroom Quiz

13th of 73 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
The Molecular Profiling and Drug Delivery (MPDD) function within the Synthetic Molecules CMC organization is accountable for a broad range of deliverables across various stages of drug discovery and development. During lead optimization and through candidate selection, MPDD scientists utilize state of the art automation and computational tools supported by expertise in biopharmaceutics, drug delivery, and solid-state chemistry to collaboratively progress candidates with higher probability of success into development and advise clinical formulation strategy. From candidate selection through clinical proof of concept and product launch, MPDD scientists work in cross functional teams to identify the commercial solid form of the active pharmaceutical ingredient (API) and establish structure-property-performance correlations to help deliver robust commercial processes and align control strategies across drug substance and product. They also transition drug substance isolation processes and relevant physical characterization methods to commercial manufacturing sites and work within teams to ensure successful regulatory submissions.
Solid State Chemist/Materials Scientist within AbbVie's MPDD organization work in cross-functional teams to support projects through all phases of development (Lead Optimization to Process Validation). In early development, they identify solid form of the active pharmaceutical ingredient (API) and develop scalable API isolation processes for early clinical studies. During Phase II, they work with engineers and formulation scientists to establish structure-property-performance correlations and deliver commercial API isolation processes with optimized physical properties. In the final stages of development, they collaboratively transition isolation processes and relevant physical characterization methods into the commercial manufacturing sites. Throughout development, they work with relevant teams to ensure successful regulatory submissions. In order to develop and implement robust solutions, Solid State Chemists/Materials Scientist at AbbVie use a very diverse set of experimental, analytical and modeling techniques and tools.
Job Description:
AbbVie's MPDD organization is seeking a highly motivated, talented, and creative scientist who is passionate in solid-state and materials characterization for an Associate Scientist I position. This person will support solid form development of clinical candidates, drug substance process development, and materials characterization spanning the drug substance and drug product interface.
Key Responsibilities:
  • Independently execute solid-state activities, including polymorph screening, salt screening, and materials characterization to support pipeline projects.
  • Support API crystallization, isolation, and milling process development to enable timely clinical deliveries with MPDD project leads.
  • Demonstrate strong data interpretation and troubleshooting skills by evaluating experiments and instrumentation, and by suggesting, designing, and pursuing relevant experiments.
  • Lead and support group safety, lab management, instrument maintenance, and overall laboratory operations to ensure efficient use of time, equipment, supplies, and reagents.
  • Learn and effectively implement new experimental techniques and protocols, while applying basic scientific principles and consulting relevant literature to place data in proper scientific context.
  • Maintain excellent documentation of all work, including electronic lab notebooks, test methods, and protocols.
  • Present results and experimental information in team meetings and communicate scientific findings clearly.
  • Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.

Qualifications
Basic:
  • BS with 0-3 years of experience in pharmaceutical or related industry. Preferred educational background includes but is not restricted to Chemical Engineering, Organic Chemistry, Physical Pharmacy, Pharmaceutical Sciences, or Materials Science.
  • Theoretical and practical knowledge to carry out job functions.

Preferred:
  • A working knowledge of drug substance physical properties, polymorphism, and solid-state characterizations (e.g. particle size, microscopy, flowability, surface area, thermal analysis, PXRD, etc.) relevant to pharmaceutical development and drug product manufacturability/stability.
  • Excellent oral and written communication skills.
  • Strong organizational, planning and troubleshooting skills.
  • Ability to work in a fast-paced environment and adapt to changing conditions.
  • Demonstrated ability to work collaboratively in a cross-functional team setting.

Key Competencies:
  • Independently generate precise, reliable and reproducible data in a timely manner.
  • Demonstrate experimental precision and strong data interpretation skills.
  • Competently perform routine tasks with attention to detail. Independently review and scrutinize both own and others' data.
  • Learn fast, grasp the "essence" and can change the course quickly where indicated.
  • Raise the bar and is never satisfied with the status quo.
  • Create a learning environment, open to suggestions and experimentation for improvement.
  • Embrace the ideas of others, nurture innovation and manage innovation to reality.
  • Keep accurate and current experiments and/or records of research according to AbbVie policies.

Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.
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 roleat the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on manyfactors 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 isearned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits thatare 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 andabsolute 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