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Cardinal Health

We currently have a career opening for a Scientist III CMC. What Chemistry, Manufacturing and Controls contributes to Cardinal Health The Scientist III CMC is a senior-level contributor responsible ...

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How much do cmc scientist jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for cmc scientist in the United States is $42.08, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $48.56 per hour, depending on experience, location, and employer.

Do pharmaceutical scientists make a lot of money?

Pharmaceutical scientists, including those working as CMC (Chemistry, Manufacturing, and Controls) scientists, typically earn competitive salaries that vary by experience, education, and location. According to industry data, the median annual salary for pharmaceutical scientists ranges from $70,000 to over $120,000, with senior roles and specialized skills commanding higher pay. Factors such as advanced degrees, certifications, and expertise in regulatory requirements can influence earning potential.

What are CMC jobs?

CMC jobs refer to roles in Chemistry, Manufacturing, and Controls within the pharmaceutical and biotech industries. These positions involve developing, manufacturing, and ensuring the quality of drug products, often requiring knowledge of regulatory standards, Good Manufacturing Practices (GMP), and laboratory skills.

What are CMC Scientists?

CMC Scientists, or Chemistry, Manufacturing, and Controls Scientists, are professionals who focus on the development, production, and quality control of pharmaceutical products. They play a critical role in ensuring that drugs are manufactured consistently, safely, and according to regulatory standards. Their responsibilities include designing experiments, analyzing data, and preparing documentation required for regulatory submissions. CMC Scientists often work closely with other departments such as regulatory affairs, quality assurance, and manufacturing to ensure product integrity throughout the drug development process.

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

To thrive as a CMC (Chemistry, Manufacturing, and Controls) Scientist, you need a strong background in chemistry, pharmaceutical sciences, or chemical engineering, typically supported by an advanced degree and industry experience. Familiarity with analytical instrumentation, regulatory submission tools, and quality management systems such as GMP are essential. Strong problem-solving, project management, and communication skills help coordinate cross-functional teams and manage complex projects. These capabilities ensure regulatory compliance, efficient development processes, and the successful delivery of safe, effective pharmaceutical products.

What are some common challenges CMC Scientists face when collaborating with cross-functional teams during drug development?

CMC Scientists often work closely with regulatory, analytical, and manufacturing teams to ensure a drug's quality and compliance throughout development. A common challenge is aligning timelines and priorities, as different teams may operate on varying schedules or have distinct objectives. Effective communication and flexibility are essential to manage the complex data requirements, address technical hurdles, and respond to regulatory feedback. By fostering strong cross-departmental relationships, CMC Scientists can help streamline processes and mitigate potential delays.

What is a CMC scientist?

A CMC scientist specializes in Chemistry, Manufacturing, and Controls (CMC) within the pharmaceutical industry, focusing on developing and ensuring the quality of drug products. They work on formulation, process development, and regulatory documentation, often using laboratory techniques and regulatory guidelines to support drug approval processes.

What is the highest paid scientist job?

In the field of CMC (Chemistry, Manufacturing, and Controls) science, senior roles such as Director of CMC or Vice President of CMC typically have the highest salaries, often exceeding $150,000 annually. These positions require extensive experience, leadership skills, and expertise in regulatory compliance and drug development processes.
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What job categories do people searching Cmc Scientist jobs look for? The top searched job categories for Cmc Scientist jobs are:
Cmc Scientist jobs near you
Global Regulatory CMC Scientist (Atlanta)

Global Regulatory CMC Scientist (Atlanta)

UCB

Atlanta, GA • Hybrid

Other

Posted 18 days ago

Job description

Make your mark for patients

We are looking for a Regulatory CMC Scientist to join us in our Global Regulatory team, based in our Raleigh, NC, or Atlanta, GA offices.

About the role

Define the strategy, planning and preparation (writing and review) of CMC submission documentation for regulatory submissions (new marketing applications, variations) from a global/regional perspective to achieve timely approvals to meet business needs.

Who you'll work with

You will work within the Regulatory CMC team and partner with other technical and regulatory functions across the business.

What you'll do

Responsible for regional and global CMC submissions in line with agreed global regulatory strategy, and within agreed timelines.

Contribute and ensure adequate provision of regulatory CMC input to all Health Authority (HA) interactions on CMC matters in all regions

Ensures effective communication of CMC regulatory strategy, risks, and overall plan to GRA Teams, Technical, Development and Commercial Teams

Highlights anticipated and ongoing critical issues arising through the product life cycle in a timely manner to senior management to enable communication to key stakeholders

Lead or contribute to ongoing process improvement and department initiatives within the CMC Regulatory Affairs function, including process improvements, SOP review and development, and evaluation/implementation of digital strategies and tools.

Interested? For this position you'll need the following education, experience and skills:

Bachelor's degree, Master's preferred in a relevant life science or business-related discipline

Demonstrated ability to leverage digital tools, structured data, and regulatory information systems to enhance CMC and Device regulatory strategy, submission quality, lifecycle management, and decisionmaking across global markets

Significant relevant experience in the pharmaceutical industry preferably in Regulatory Affairs CMC with focus on biological entities

Proven track record of successful authoring and contribution to delivering CMC sections of marketing authorisations for new biological entities

Knowledge of GMP requirements, standard systems (e.g. change management systems and tools)

Effective interpersonal, presentation and communication skills with established internal and external stakeholders

Proven leadership, problem-solving ability, flexibility, influence, and effective teamwork skills.

Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer.All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.


Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Employment Type: OTHER

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