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Cmc Scientist Jobs (NOW HIRING)

Founded in 2002, Tang Capital is a life-sciences focused investment company that creates, acquires ... Position Summary The Director, CMC - Formulations will contribute to the oversight, planning and ...

CMC Writer

Paramus, NJ ยท On-site

CMC Writer Job Location: Paramus, NJ Job Type: Contract * Authors a range of clinical documents ... Work closely with scientists, regulatory affairs teams, and manufacturing experts to gather ...

CMC Writer

Paramus, NJ ยท On-site

$45 - $50/hr

CMC Writer Location: Paramus, New Jersey, 07652 Job Type: Contract Duration: 6 Months Work Type ... Work closely with scientists, regulatory affairs teams, and manufacturing experts to gather ...

CMC Regulatory Lead

Redwood City, CA ยท On-site

$200K - $240K/yr

Have a bachelor's degree in a life sciences discipline or equivalent (advanced degree preferred). * 7+ years of hands-on experience in regulatory CMC. * Demonstrated experience leading CMC regulatory ...

The ideal candidate possesses strong analytical chemistry/scientific expertise, excellent technical writing capabilities, a proven track record in CMC or analytical development for pharmaceuticals ...

Director, Regulatory CMC

Waltham, MA ยท On-site

$161K - $213K/yr

Lead and execute global CMC regulatory strategies for assigned programs across all phases of ... Bachelor's degree in life sciences or a related scientific discipline required; advanced degree ...

CMC Manager Duration: 12 Months Location: Morristown, NJ 07962 The CMC Documentation Team is ... Demonstrated ability/experience managing IT based scientific systems Thanks & Regards, Mayank Gupta ...

Director, Regulatory CMC

Waltham, MA ยท On-site

$161K - $213K/yr

Lead and execute global CMC regulatory strategies for assigned programs across all phases of ... Bachelor's degree in life sciences or a related scientific discipline required; advanced degree ...

Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose ... The Director of Regulatory CMC will lead the development and execution of global CMC regulatory ...

Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose ... The Director of Regulatory CMC will lead the development and execution of global CMC regulatory ...

OR ยท On-site

BA or BS degree in Science, Mathematics, Engineering, or a related scientific discipline required * 10+ years of relevant radiopharmaceutical/pharmaceutical/biopharma CMC experience with 5+ years of ...

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Cmc Scientist information

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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.
More about Cmc Scientist jobs

Director, CMC - Formulations

Codera

San Diego, CA โ€ข Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 26 days ago


Job description

Salary: 190,000 - 260,000

About Codera

Codera is a Tang Capital company that provides in-house, end-to-end drug development capabilities for its portfolio companies. Founded in 2002, Tang Capital is a life-sciences focused investment company that creates, acquires and finances companies that develop and commercialize pharmaceutical products.


Position Summary

The Director, CMC - Formulations will contribute to the oversight, planning and execution of Chemistry, Manufacturing and Controls (CMC) strategy, including drug product formulations, in support of Coderas development programs. In collaboration with internal departments, such as nonclinical, clinical pharmacology and regulatory teams, the Director, CMC - Formulations will contribute to all aspects of chemistry, manufacturing and controls, including design of drug product formulations, oversight of vendors and production of regulatory documents.


Essential Duties and Responsibilities

  • Assist with the design and evaluation of drug product formulations, primarily small molecule formulations, to achieve specific pharmacokinetic (PK) goals
  • Contribute to CMC and development strategy
  • Manage relationships with various contract development and manufacturing organizations (CDMOs), analytical labs and contract research organizations (CROs)
  • Assist with the clinical supply logistics
  • Prepare, analyze and interpret analytical data that integrate into regulatory and intellectual property (IP) documents
  • Draft, edit and review sections of regulatory and IP documents
  • Provide scientific input for analytical protocols and study reports
  • Contribute to a fast-paced, dynamic, data-driven scientific culture that embraces innovation and excellence
  • Research CMC and formulation topics to support Tang Capitals investments
  • Participate in business development activities, as requested


Qualifications

  • Bachelors degree or higher in life sciences or related discipline required
  • Masters degree preferred
  • Minimum of 5 years in relevant pharmaceutical industry work experience required
  • Experience with small molecule formulations required
  • Experience with biologics formulations preferred
  • Experience working with CDMOs and analytical labs
  • Experience with one or more of the following drug product formulation strategies: modified/delayed release, fixed-dose combinations, spray-dried dispersions
  • Experience with a wide range of excipients and formulation technologies
  • Experience with formulations for oral, subcutaneous and/or inhaled delivery
  • Ability to research, synthesize and summarize complex CMC topics
  • Experience writing and/or reviewing regulatory documents, including Investigational New Drug (IND)/New Drug Application (NDA) sections
  • Ability to effectively organize and manage multiple assignments with challenging timelines from project start-up through submission
  • Excellent knowledge of Food and Drug Administration (FDA) and International Council for Harmonisation (ICH) regulations and Good Manufacturing Practices (GMP)
  • Outstanding written and verbal communication skills, including the ability to use clear language to explain complex ideas
  • Ability to establish and maintain collaborative working relationships with internal and external stakeholders



The job description is not designed to cover or contain a comprehensive list of activities, duties or responsibilities that are required. They may change, or new ones may be assigned at any time with or without notice.


The estimated annual base salary for this position is $190,000 - $260,000, commensurate with experience and skills. This role may be eligible for discretionary bonuses and other incentive programs.


Codera provides a comprehensive benefits package designed to support employees physical, mental and financial health and include employer sponsored insurance plans including medical, dental and vision coverage; generous paid time off; retirement plan options and additional wellness and professional development programs


Codera provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.


Codera participate in EVerify. All newly hired employees are required to complete the EVerify process as part of their employment eligibility verification.