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Cmc Scientist Jobs (NOW HIRING)

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 ...

Cardinal Health

$31.50 - $40.41/hr

We currently have a career opening for a Scientist I - CMC What Chemistry, Manufacturing and Controls contributes to Cardinal Health The Scientist I - CMC supports regulatory activities for pre ...

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How much do cmc scientist jobs pay per hour?

As of Jul 28, 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
Infographic showing various Cmc Scientist job openings in the United States as of July 2026, with employment types broken down into 2% Internship, 1% As Needed, 80% Full Time, 14% Part Time, 2% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $87,519 per year, or $42.1 per hour.
Global Regulatory CMC Scientist (Raleigh)

Global Regulatory CMC Scientist (Raleigh)

UCB

Raleigh, NC • On-site

Full-time

Posted 10 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 decision-making 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.
Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities.
Unless explicitly stated in the description, this role is hybrid with 40% of your time spent in the office, regardless of your current contractual agreement. If your current working arrangements differ, please contact your Talent Partner to discuss before submitting your application.
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.
Requisition ID: 93424
Recruiter: Kevin Ross
Hiring Manager: Wanja Muthoga
Talent Partner: Bianca Hinshaw
Job Level: MM II
Please consult HRAnswers for more information on job levels.

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