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How much do cmc operations jobs pay per hour?

As of Aug 1, 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 3% Locum Tenens, 26% Internship, 55% Full Time, 9% Part Time, 2% Contract, and 5% Summer. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $54,588 per year, or $26.2 per hour.

Manager, CMC Operations Program Management

ElevateBio

Waltham, MA • Hybrid

Other

Posted 8 days ago

Job description

The Role:

The Manager, CMC Operations and Program Management will lead the cross-functional activities between CMC groups and other departments at ElevateBio BaseCamp including process development, analytical development, facilities and engineering, MSAT, manufacturing and supply chain within the scope of various programs.  The Manager will be a part of the BaseCamp CMC and Program Management department and will aid in supporting both internal portfolios at BaseCamp. This position will contribute to ensuring alignment with corporate goals and timelines. The position is hybrid with 2-3 days onsite a week.

 

Here's What You'll Do:

  • Build and maintain strong internal relationships with SMEs at Base Camp (PD, MSAT, Manufacturing, AD/QC, QA, Regulatory, Commercial) and external relationships with scientific and program management staff at partner organization to ensure program goals and accountabilities 
  • Develop, maintain and track CMC project plans (e.g., detailed Gantt, budget, resources, etc.) with SMEs to encompass key program milestones and deliverables in alignment with overall program objectives with experience/familiarity in the following: 
  • Autologous / allogeneic cell therapy tech transfers
  • Facilitate internal CMC team meetings and meetings with BaseCamp partners using meeting management best practices (both what and how) to drive cross-functional communication, timely and effective decision-making, and successful execution of program activities  
  • Proactively identify risks, gaps, and resource bottlenecks, and work with impacted teams to develop and implement mitigation plans 
  • Generate dashboards indicating key program milestones, updates, risks and challenges
  • Maintain risk registers, decision logs, and change requests
  • Help prepare content for Joint Leadership Meetings
  • Support the standardization of processes and communication(s) in order to build efficiencies within the department 
  • Contribute to the management and review of KPIs at BaseCamp 
  • Hold weekly 1:1s with BaseCamp partner counterparts to ensure program milestones are being met
  • Work closely with finance and department leads for invoicing

Requirements:

  • S. in a scientific or engineering discipline
  • 3 or more years of relevant experience in the CMC environment. Cell/gene therapy preferred.
  • cGMP program management experience is required
  • Strong understanding of US FDA and EU EMA regulations and ICH guidelines for cell and gene therapy products is preferred
  • Extensive experience is leading product/process program within a GMP setting
  • Program management skills, including strategic and tactical programs/tasks, tracking and adhering to budgets, reporting program and campaign metrics, and other program management tools
  • Strong verbal and written skills are required as well as effective interpersonal, technical, and troubleshooting skills
  • Outstanding planning, organization, and multitasking skills

The budgeted range for this position is $125,000 - $165,000. This range is a good faith estimate of the expected salary range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law. 

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