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Cmc Jobs in California (NOW HIRING)

Vaxcyte

Associate Director, Regulatory CMC

San Carlos, CA · On-site

$180K - $210K/yr

Provides regulatory CMC guidance to various cross-functional teams and ensures all applicable global regulatory requirements are considered and incorporated into product development. Conducts routine ...

Codera LLC

Director, CMC - Formulations

San Diego, CA · On-site

$190K - $260K/yr

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 ...

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Cmc information

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$13

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$66

How much do cmc jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for cmc in California is $30.83, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $36.06 per hour, depending on experience, location, and employer.

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

To thrive as a CMC professional, you need expertise in pharmaceutical sciences, regulatory requirements, and process development, typically supported by a degree in chemistry, pharmacy, or a related field. Familiarity with regulatory submission systems, analytical tools, and quality management software is essential. Strong project management, attention to detail, and effective communication are vital soft skills for coordinating cross-functional teams and ensuring compliance. These skills and qualities are critical to guarantee the safety, efficacy, and regulatory approval of pharmaceutical products.

What are some common challenges faced by a CMC professional when coordinating between R&D, manufacturing, and regulatory teams?

CMC professionals often encounter challenges in aligning the timelines and priorities of R&D, manufacturing, and regulatory teams. Ensuring that product development meets both regulatory requirements and manufacturing feasibility can require extensive cross-functional communication and problem-solving. Additionally, adapting to evolving regulatory guidelines and integrating feedback from multiple stakeholders demands strong project management skills. Overcoming these challenges is essential for maintaining project momentum and ensuring successful product submissions.

What is a CMC?

CMC stands for Chemistry, Manufacturing, and Controls. CMC professionals are responsible for ensuring that pharmaceutical products are developed, manufactured, and controlled in compliance with regulatory standards. Their work includes overseeing formulation development, analytical testing, process validation, and documentation required for regulatory submissions. CMC experts play a critical role in bringing safe and effective drugs to market by ensuring product quality and consistency throughout the development and manufacturing process.

What is the difference between CMC vs Regulatory Affairs Specialist?

AspectCMCRegulatory Affairs Specialist
Required CredentialsBachelor's degree in life sciences, chemistry, or pharmacy; often additional certifications in pharmaceutical sciencesBachelor's degree in life sciences, pharmacy, or related field; certifications in regulatory affairs are common
Work EnvironmentLaboratories, manufacturing sites, and R&D departments within pharmaceutical companiesRegulatory agencies, pharmaceutical companies, and consulting firms
Industry UsageFocuses on drug development, manufacturing, and quality documentationFocuses on compliance, submissions, and communication with regulatory bodies

While both CMC and Regulatory Affairs Specialists work within the pharmaceutical industry, CMC professionals primarily handle the chemistry, manufacturing, and control aspects of drug development. Regulatory Affairs Specialists focus on ensuring compliance with regulations and managing submissions to authorities. Both roles often collaborate but serve distinct functions in bringing a drug to market.

What are the most commonly searched types of Cmc jobs in California? The most popular types of Cmc jobs in California are:
What are popular job titles related to Cmc jobs in California? For Cmc jobs in California, the most frequently searched job titles are:
What job categories do people searching Cmc jobs in California look for? The top searched job categories for Cmc jobs in California are:
What cities in California are hiring for Cmc jobs? Cities in California with the most Cmc job openings:
Cmc jobs near you
Infographic showing various Cmc job openings in California as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $64,135 per year, or $30.8 per hour.

Vice President, Global CMC Regulatory

Revolution Medicines

Redwood City, CA • Hybrid

$183K - $242K/yr

Other

Re-posted 3 days ago

Job description

The Opportunity:

We are seeking an accomplished, strategic and execution-oriented leaders, Vice President, Global CMC Regulatory, reporting to SVP of Pharmaceutical Development and Manufacturing (PDM) Regulatory, to lead our global chemistry, manufacturing, and controls (CMC) regulatory strategy and execution across all development programs and commercial assets.  This leader will drive regulatory strategy development, lead regulatory interactions, and provide expertise throughout the product lifecycle, from early development to post-approval variations ensuring the timely submission and approval of high-quality CMC regulatory filings to support our company's pipeline and global growth. 

The successful candidate will serve as a senior leadership role within Pharmaceutical Development and Manufacturing (PDM) organization, overseeing CMC regulatory activities and ensuring alignment with health authority expectations globally (FDA, EMA, PMDA, NMPA, etc.).    The role requires expertise in small molecule pharmaceutical development and manufacturing, an understanding of the oncology development lifecycle, and the ability to thrive in a dynamic, fast-paced environment.

Responsibilities:

Global CMC Regulatory Strategy

  • Develop and execute global CMC regulatory strategies in alignment with product development plans for clinical and commercial programs / marketed products.

  • Provide strategic CMC regulatory leadership to support global filings, approvals, and post-approval lifecycle management.

  • Proactively identify and manage CMC regulatory risks, anticipate challenges and develop mitigation strategies to support business objectives and ensure global alignment and compliance.

Health Authority Engagement

  • Serve as the primary CMC regulatory interface with global health authorities, including FDA, EMA, EU National Competent Authorities, and PMDA.

  • Lead and support CMC-related regulatory meetings, scientific advice, and responses to health authority questions.

Regulatory Submissions & Lifecycle Management

  • Oversee the preparation, review, and submission of high-quality CMC sections for NDAs, MAAs, J-NDAs, and global post-approval variations.

  • Ensure consistency, compliance, and scientific rigor across global CMC regulatory filings.

  • Provide strategic oversight for post-approval changes, including site changes, process improvements, and supply chain optimization.

  • Interpret and apply evolving CMC regulatory requirements and guidance globally.

Cross-Functional Collaboration

  • Partner closely with Drug Substance, Drug Product, Analytical Development and QC, Manufacturing, Supply Chain, Quality, and Program Management to align regulatory strategy with technical and operational plans.

  • Act as a regulatory subject matter expert for tech transfer, global site registration, comparability protocols and control strategy development.

Team Development & Leadership

  • Build, mentor, and lead a high-performing global CMC regulatory team, fostering accountability, development, and innovation.

  • Manage external regulatory consultants and regional partners to ensure consistent global execution and local expertise.

Required Skills, Experience and Education:

  • Advanced degree (PhD, PharmD, or MS) in Chemistry, Pharmaceutical Sciences or related scientific discipline.

  • Minimum of 18 years of experience in the biotech/pharmaceutical industry, with at least 10 years in CMC regulatory affairs and global submission experience.

  • Demonstrated success leading global CMC regulatory strategies for small-molecule products.

  • Proven success scaling CMC regulatory function in a public, late-stage biotech/pharma company.

  • Deep understanding of global regulatory frameworks and guidelines (FDA, ICH, EMA, PMDA, NMPA, etc.).

  • Strong leadership and collaboration skills with a demonstrated ability to work cross-functionally and influence stakeholders at all levels.

  • Strong written and verbal communication skills, with the ability to clearly articulate regulatory strategy and risk.

  • Ability to thrive in a fast-paced, matrixed, and science-driven environment.

Preferred Skills:

  • Experience with oncology development programs and familiarity with accelerated or expedited pathways.

  • Experience with Japan-specific CMC regulatory requirements (e.g., consultations, GQP/GMP compliance, J-NDA format).

  • Exposure to lifecycle management activities including global variations, site changes, and supply chain adaptations. 

    #LI-Hybrid  #LI-GL1

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