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How much do cmc operations jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for cmc operations in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $30.29 per hour, depending on experience, location, and employer.

What are CMC operations?

CMC operations refer to the activities involved in Chemistry, Manufacturing, and Controls within the pharmaceutical industry, focusing on the development, production, and quality assurance of drug products. Professionals in this field ensure compliance with regulatory standards and often work with laboratory techniques, documentation, and process validation.

What are CMC jobs?

CMC jobs refer to roles in Chemistry, Manufacturing, and Controls within the pharmaceutical and biotech industries. These positions involve developing, validating, and overseeing manufacturing processes, ensuring compliance with regulatory standards, and preparing documentation for drug approval. Skills in quality assurance, regulatory knowledge, and technical expertise are often required.

Is CMC a good career path?

CMC Operations involves managing chemistry, manufacturing, and controls processes in the pharmaceutical industry, requiring knowledge of regulatory standards and quality assurance. It offers opportunities for career growth, especially for those with a background in science, engineering, or quality management. The role often involves collaboration across departments and adherence to strict compliance requirements.

Are CMC jobs in high demand?

CMC operations roles are in steady demand within the pharmaceutical and biotech industries due to the need for compliance, quality control, and process management in drug development. These positions often require knowledge of regulatory standards and experience with manufacturing processes, making them valuable for candidates with relevant skills and certifications.

What is the difference between Cmc Operations vs CMC Regulatory Affairs?

AspectCmc OperationsCMC Regulatory Affairs
Required CredentialsBachelor's degree in life sciences, engineering, or related field; experience in manufacturing or quality controlDegree in life sciences, pharmacy, or related; regulatory certifications often preferred
Work EnvironmentManufacturing plants, quality control labs, supply chainRegulatory agencies, corporate offices, compliance teams
Industry UsageManufacturing, quality assurance, supply chain managementRegulatory submissions, compliance, documentation
Common Search/ComparisonYesYes

While both Cmc Operations and CMC Regulatory Affairs are essential in the pharmaceutical industry, Cmc Operations focuses on manufacturing, quality control, and supply chain processes. In contrast, CMC Regulatory Affairs handles regulatory submissions, compliance, and documentation to ensure products meet legal standards. Understanding these differences helps professionals and employers align roles with their expertise and industry needs.

What cities are hiring for Cmc Operations jobs? Cities with the most Cmc Operations job openings:
What states have the most Cmc Operations jobs? States with the most job openings for Cmc Operations jobs include:
What job categories do people searching Cmc Operations jobs look for? The top searched job categories for Cmc Operations jobs are:
Cmc Operations jobs near you
Infographic showing various Cmc Operations job openings in the United States as of July 2026, with employment types broken down into 35% Internship, 1% As Needed, 50% Full Time, 8% Part Time, 1% Contract, and 5% Summer. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $54,588 per year, or $26.2 per hour.

Director, CMC Project Management (Biologics)

Enigma Search

Redwood City, CA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Director, CMC Project Management (Biologics) About Our Client

Our client is stealth stage biopharmaceutical company dedicated to developing next-generation antibody biotherapeutics. They are currently seeking a highly skilled and strategicBiologics CMC Project Manager to spearhead their chemistry, manufacturing, and controls (CMC) operations from Post-Candidate Selection (PCC) through IND submission.

This is a fantastic opportunity to join a lean, high-performing team where your leadership will directly impact the acceleration of life-changing therapies to clinical trials.

Responsibilities
  • Develop comprehensive project plans, timelines, and budgets for biologics CMC development projects from PCC nomination to IND submission.
  • Participate in screening, selection, and qualification of Contract Development and Manufacturing Organizations (CDMOs) for various biotherapeutic modalities including mAb, BsAb, TsAb, fusion protein, protein conjugates etc.
  • Support due diligence efforts associated with CMC development activities, support service contract negotiations and other CDMO related activities.
  • Drive multidisciplinary CMC teams, including cell line development, upstream and downstream process development, formulation development, analytical method development and qualification, drug substance and drug product manufacturing, quality control, regulatory filing, and supply chain management to maximize the value of development work and ensure effective communications and quality decisions.
  • Keep all the stakeholders fully apprised of project status and issues at the right level of detail. Understand and elevate issues to teams and stakeholders appropriately.
  • Identify technical gaps in development and manufacturing and implement proactive remediations and strategies to ensure project success.
  • Ensure adherence to regulatory requirements for both development and manufacturing activities.
Requirements
  • BS/BA and above degree in biochemistry, biochemical engineering or other life science disciplines.
  • Minimum of 10+ years of biologic therapeutic development / commercialization experience with BS/BA degree or minimum of 6+ years biologic therapeutic development experience with an advanced degree.
  • Demonstrated deep understanding and experience in biologic modality drug development and manufacturing processes for mAb, BsAb, TsAb, fusion protein, protein conjugates etc.
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