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Pharmaceutical Cmc Jobs (NOW HIRING)

NY ยท On-site

$120 - $190/hr

Partner with pharmaceutical CMC clients to identify high-value opportunities for computational modeling, advanced analytics, and AI/ML across process development, scale-up, manufacturing, and ...

New

$120 - $190/hr

Partner with pharmaceutical CMC clients to identify high-value opportunities for computational modeling, advanced analytics, and AI/ML across process development, scale-up, manufacturing, and ...

New

CMC Writer

Paramus, NJ ยท On-site

$45 - $50/hr

Hybrid * A Pharmaceutical CMC (Chemistry, Manufacturing, and Controls) Writer plays a crucial role in regulatory submissions by preparing technical documents related to drug development ...

The primary responsibility of this role is to deliver projects in the pharmaceutical CMC development area for ZS clients. This includes serving as a subject matter expert on drug substance and drug ...

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Pharmaceutical Cmc information

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$14

$19

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How much do pharmaceutical cmc jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for pharmaceutical cmc in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What is a pharmaceutical CMC?

Pharmaceutical CMC professionals are experts who manage the Chemistry, Manufacturing, and Controls (CMC) aspects of drug development and production. They ensure that pharmaceuticals are consistently manufactured with the required quality, safety, and efficacy by overseeing the development, scale-up, and regulatory submission processes. Their work involves coordinating formulation, analytical testing, process validation, and compliance with regulatory guidelines, such as those from the FDA or EMA. CMC professionals play a critical role in bringing new drugs to market by ensuring all manufacturing and quality controls meet stringent regulatory standards.

What skills and qualifications are needed to thrive as a pharmaceutical CMC?

To thrive as a Pharmaceutical CMC professional, you need a strong background in chemistry, pharmaceutical sciences, and regulatory compliance, often supported by a relevant degree or advanced qualification. Familiarity with regulatory submission systems (e.g., eCTD), analytical instrumentation, and quality management systems is typically required. Critical thinking, attention to detail, and effective cross-functional communication are vital soft skills for excelling in this role. These skills ensure that pharmaceutical products are developed, manufactured, and documented in compliance with global regulations, supporting product quality and successful regulatory approvals.

What are common challenges faced in a pharmaceutical CMC role, and how can they be addressed?

One of the main challenges in a Pharmaceutical CMC role is ensuring regulatory compliance while managing tight timelines for product development and approval. Professionals must coordinate across cross-functional teams, including R&D, quality assurance, and manufacturing, to ensure all documentation and processes meet evolving regulatory standards. Staying updated with global regulatory requirements and maintaining clear communication channels can help address these challenges. Additionally, adaptability and strong project management skills are essential to navigate unexpected technical or regulatory hurdles that may arise during the drug development lifecycle.

What is the difference between Pharmaceutical Cmc vs Pharmaceutical Quality Assurance?

AspectPharmaceutical CmcPharmaceutical Quality Assurance
Primary FocusDevelopment, manufacturing, and control of drug substances and productsEnsuring product quality through audits, compliance, and process validation
Required CredentialsDegree in pharmacy, chemistry, or related field; knowledge of GMP regulationsDegree in pharmacy, chemistry, or related field; understanding of quality systems
Work EnvironmentLaboratories, manufacturing sites, R&D facilitiesQuality control labs, regulatory agencies, manufacturing oversight
Industry UsageDrug development, formulation, manufacturingQuality management, compliance, validation processes

Pharmaceutical Cmc professionals focus on the development and manufacturing of drug substances, ensuring formulation and process control. In contrast, Pharmaceutical Quality Assurance specialists concentrate on maintaining product quality through audits, validation, and compliance. Both roles require similar educational backgrounds and work within the pharmaceutical industry, but their core responsibilities differ significantly.

What cities are hiring for Pharmaceutical Cmc jobs?

Cities with the most Pharmaceutical Cmc job openings:

What states have the most Pharmaceutical Cmc jobs?

States with the most job openings for Pharmaceutical Cmc jobs include:

Infographic showing various Pharmaceutical Cmc job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Computational Modeling Associate Consultant - CMC

ZS

Chicago, IL โ€ข On-site

$120K - $137K/yr

Full-time

This job post hasย expired today.ย Applications are no longer accepted.


Job description

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning, bold ideas, courage and passion to drive life-changing impact to ZS.
Insights & Analytics
ZS's Insights & Analytics group partners with clients to design and deliver solutions to help them tackle a broad range of business challenges. Our teams work on multiple projects simultaneously, leveraging advanced data analytics and problem-solving techniques. Our recommendations and solutions are based on rigorous research and analysis underpinned by deep expertise and thought leadership.
ZS is seeking a Computational Modeling Expert to help pharmaceutical clients apply advanced modeling, simulation, and AI/ML to complex CMC and process development challenges. In this role, you will combine deep scientific and engineering expertise with first-principles and data-driven modeling to improve process understanding, accelerate development, support scale-up and technology transfer, and enable more informed decision-making. You will work closely with scientists, engineers, data teams, and senior CMC stakeholders to translate complex technical questions into scalable computational solutions that can be integrated into real-world scientific and manufacturing workflows.
What You'll Do
  • Partner with pharmaceutical CMC clients to identify high-value opportunities for computational modeling, advanced analytics, and AI/ML across process development, scale-up, manufacturing, and technology transfer.
  • Develop and apply first-principles and mechanistic models, including CFD, DEM, computational chemistry, and other physics-based approaches, to solve complex CMC and process development challenges.
  • Build and apply AI/ML models that complement first-principles approaches and improve process understanding, prediction, optimization, and decision-making.
  • Translate scientific and business questions into modeling strategies, analytical approaches, and implementation plans.
  • Assess available experimental, process, and manufacturing data and determine the appropriate data, modeling methods, and computational techniques required to address client needs.
  • Develop robust, reusable, and production-ready modeling solutions, including code development, testing, deployment, documentation, versioning, and ongoing model lifecycle management.
  • Integrate computational models with relevant CMC data sources and systems, including ELN, LIMS, ERP, and PLM platforms.
  • Interpret modeling results and translate complex technical findings into clear recommendations for scientists, engineers, and senior CMC leaders.
  • Support model validation, adoption, and integration into scientific and operational workflows.
  • Apply modeling expertise across modalities and manufacturing processes, adapting approaches to new scientific and technical challenges as needed.
  • Lead technical workstreams and collaborate with multidisciplinary teams across process development, data science, engineering, manufacturing, and technology.
  • Contribute to the development of ZS capabilities, methodologies, and reusable assets in computational modeling and digital CMC.

What You'll Bring
  • Bachelor's, Master's, or PhD in Chemical Engineering, Mechanical Engineering, Materials Science, Chemistry, Biotechnology, Computational Science, or a related quantitative or scientific discipline.
  • At least 2.5 years of relevant experience, preferably within pharmaceutical CMC, process development, manufacturing, or a closely related environment.
  • Hands-on experience developing first-principles or mechanistic models, such as CFD, DEM, computational chemistry, process models, or other physics-based modeling approaches, for pharmaceutical process development or manufacturing.
  • Experience developing and applying AI/ML models to scientific, engineering, or process development problems.
  • Strong programming skills and experience developing production-quality modeling code and managing models across their lifecycle.
  • Strong understanding of pharmaceutical CMC concepts, including unit operations, process development, Quality by Design, technology transfer, process validation, critical quality attributes, and development and regulatory milestones.
  • Experience working with scientific and manufacturing data and familiarity with systems such as ELN, LIMS, ERP, or PLM.
  • Ability to combine first-principles modeling, data-driven modeling, and domain expertise to solve complex scientific and engineering problems.
  • Ability to translate modeling approaches and technical results into clear business and scientific recommendations.
  • Experience communicating with senior scientific, technical, and business stakeholders.
  • Ability to lead multiple technical workstreams and effectively manage priorities, timelines, and deliverables.
  • Ability to apply expertise developed in one modality or process area to new modalities and scientific contexts.
  • Fluency in English
  • Client-first mentality
  • Intense work ethic
  • Collaborative spirit and problem-solving approach

Preferred Qualifications
  • Advanced degree in a relevant engineering, scientific, or computational discipline.
  • Experience with hybrid modeling approaches that combine mechanistic models with AI/ML.
  • Experience deploying computational models into production or decision-support environments.
  • Familiarity with CMC regulatory submission requirements and expectations for model validation, traceability, and documentation.
  • Experience across multiple pharmaceutical modalities, such as small molecules, biologics, cell and gene therapies, or other advanced therapies.
  • Consulting or client-facing experience in pharmaceutical R&D, CMC, or manufacturing.

How you'll grow:
  • Cross-functional skills development & custom learning pathways
  • Milestone training programs aligned to career progression opportunities
  • Internal mobility paths that empower growth via s-curves, individual contribution and role expansions

Perks & Benefits:
At ZS, your growth matters. We offer a comprehensive total rewards package that supports your health and well-being, financial future, time away, and professional development. With robust skills-building programs, multiple career progression paths, internal mobility, and a deeply collaborative culture, you'll have the opportunity to do meaningful work, expand your capabilities, and thrive as part of a global community. For details on total rewards in United States, visit ZS US office locations | Where we work | ZS.
Hybrid working model:
We are committed to giving our employees a flexible and connected way of working. A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS offices for the majority of our week. The magic of ZS culture and innovation thrives in both planned and spontaneous face-to-face connections.
Travel:
Travel is a requirement at ZS for client facing ZSers; business needs of your project and client are the priority. While some projects may be local, all client-facing ZSers should be prepared to travel as needed. Travel provides opportunities to strengthen client relationships, gain diverse experiences, and enhance professional growth by working in different environments and cultures.
Considering applying?
At ZS, we honor the visible and invisible elements of our identities, personal experiences, and belief systems-the ones that comprise us as individuals, shape who we are, and make us unique. We believe your personal interests, identities, and desire to learn are integral to your success here. We are committed to building a team that reflects a broad variety of backgrounds, perspectives, and experiences. Learn more about our inclusion and belonging efforts and the networks ZS supports to assist our ZSers in cultivating community spaces and obtaining the resources they need to thrive.
If you're eager to grow, contribute, and bring your unique self to our work, we encourage you to apply.
ZS is an equal opportunity employer and is committed to providing equal employment and advancement opportunities without regard to any class protected by applicable law.
Work Authorization:
This position is not eligible for visa sponsorship. Candidates must have authorization to work in the United States that does not now or in the future require employer sponsorship.
To complete your application:
An on-line application, including a full set of transcripts (official or unofficial), is required to be considered.
NO AGENCY CALLS, PLEASE.
Find Out More At:
www.zs.com

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About ZS

Sourced by ZipRecruiter

Industry

Business management consulting

Company size

10,000+ Employees

Headquarters location

Evanston, IL, US

Year founded

1983