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Formulation Development Cmc Jobs in Naperville, IL

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Formulation Development Cmc information

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$29

$50

$96

How much do formulation development cmc jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for formulation development cmc in Naperville, IL is $50.81, according to ZipRecruiter salary data. Most workers in this role earn between $34.57 and $81.35 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 Naperville, IL look for? The top searched job categories for Formulation Development Cmc jobs in Naperville, IL are:
What cities near Naperville, IL are hiring for Formulation Development Cmc jobs? Cities near Naperville, IL with the most Formulation Development Cmc job openings:
Formulation Development Cmc jobs near you
Infographic showing various Formulation Development Cmc job openings in Naperville, IL as of July 2026, with employment types broken down into 2% Locum Tenens, 24% Internship, 58% Full Time, 12% Part Time, 2% Contract, and 2% Summer. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $105,691 per year, or $50.8 per hour.
Director/Senior Director, Program Leadership

Director/Senior Director, Program Leadership

EVOZYNE INC

Chicago, IL • Remote

$175K - $250K/yr

Full-time

Posted 6 days ago

Job description

Evozyne is an AI-native biotech company building a new way to design therapeutic proteins. Our generative AI platform was purpose-built to create entirely novel proteins that expand what’s possible beyond traditional drug discovery. We are applying this platform to develop transformative therapies for serious diseases with significant unmet need, working at the intersection of AI, biology, and protein engineering to solve complex scientific problems that conventional approaches cannot easily address.

As the Director/Senior Director, Program Leadership, you will own the operations and execution of advancing assets through IND-enabling studies, CMC, and regulatory submission across multiple programs. You will play a central role in moving programs efficiently toward the clinic while helping shape how program leadership operates and scales within the company.

Reporting to the Chief Operating Officer, you will bring deep experience in preclinical program leadership, strong strategic and operational judgment, and clear communication to ensure programs progress effectively across complex, interdependent workstreams.

Location: Remote

What You’ll Do

  • Own the full program lifecycle from candidate nomination through IND clearance and Phase 1 enablement across multiple assets in parallel
  • Drive the critical path, including timelines, budgets, dependencies, and decision points
  • Build and maintain integrated development plans spanning nonclinical, CMC, analytical, formulation, and regulatory workstreams
  • Translate program progress into clear, actionable updates and recommendations for leadership
  • Own external partnerships with CROs and CDMOs, including vendor selection, scope definition, and ongoing performance management
  • Negotiate scope, cost, timelines, and deliverables and hold partners accountable to outcomes
  • Coordinate across multiple vendors simultaneously, managing handoffs, data flow, and interdependencies
  • Partner with internal technical experts to design studies and translate program needs into effective external workstreams
  • Oversee development of study protocols, incorporating cross-functional input and aligning stakeholders
  • Build the internal playbooks, processes, and operating structures needed to scale program execution across the pipeline

Who You Are

You are the central operator in all aspects of advancing IND programs, bringing in internal stakeholders, external consultants, and technical partners as needed. You thrive in a dynamic environment where you’re balancing speed, cost, and risk to ensure successful IND submissions. You think big on high-level regulatory and technical strategy while maintaining the attention to detail required to plan multiple steps ahead. You have a strong ownership mentality acting as the operational leader for our development programs.

Required Experience

  • Direct operational ownership of multiple IND programs in biologics, with at least one specifically in functional protein therapeutics
  • Advanced degree in biochemical, pharmacology, toxicology or related field such as biology and life sciences
  • 8+ years (Ph.D.) to 12+ years (Master’s) of relevant industry experience
  • Demonstrated success leading programs through CROs and CDMOs, including global vendors.
  • Deep understanding of the drug development process from discovery through IND filing
  • Strong familiarity with GxP, ICH guidelines, and FDA preclinical requirements
  • Proven ability to align and influence stakeholders across functions and organizations

What We’re Looking For

  • Strong strategic and operational judgment
  • Clear, concise communicator who can simplify complex programs
  • Highly organized and detail-oriented, with the ability to anticipate challenges
  • Hands-on leader who is comfortable owning outcomes directly
  • Effective at influencing without formal authority
  • Comfortable operating in a fast-moving, evolving environment

Why Evozyne

  • Opportunity to drive multiple programs from early development through IND and into the clinic in a highly integrated, fast-moving environment 
  • Ability to work at the intersection of AI, biology, and experimental science on problems where the path forward is not always clear 
  • Significant ownership and influence on how programs are executed, prioritized, and scaled as the pipeline grows 
  • Exposure to both strategic decisions and hands-on execution in a lean team where your work directly impacts program outcomes

Additional Information
Compensation Range: $175,000 - $250,000. 

Individual compensation within this range is determined by a combination of factors, including but not limited to level, years of relevant job-related experience, and internal equity. This is what we believe in good faith is the range of possible base salary for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future.

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