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Cmc Operations Jobs (NOW HIRING)

Retro

CMC Regulatory Lead

Redwood City, CA · On-site

$200K - $240K/yr

We're hiring an experienced CMC Regulatory Lead to own the strategy and operations for our Chemistry, Manufacturing, and Controls (CMC) regulatory work. As one of the earliest members of the ...

CMC

Lead Network Operations Engineer

Irving, TX · On-site

CMC is a Fortune 500 ® company that specializes in construction reinforcement and steel products. They are seeking a Lead Network Operations Engineer to oversee network operations, manage service ...

Retro

CMC Regulatory Lead

Redwood City, CA · On-site

$200K - $240K/yr

We're hiring an experienced CMC Regulatory Lead to own the strategy and operations for our Chemistry, Manufacturing, and Controls (CMC) regulatory work. As one of the earliest members of the ...

Retro

CMC Regulatory Lead

Redwood City, CA · On-site

$200K - $240K/yr

We're hiring an experienced CMC Regulatory Lead to own the strategy and operations for our Chemistry, Manufacturing, and Controls (CMC) regulatory work. As one of the earliest members of the ...

Atomic

CMC Consultant

Indomo is seeking an experienced CMC consultant to execute Chemistry, Manufacturing & Controls (CMC) strategy and operations on a fractional basis. This individual will play a critical role in ...

AbbVie

Director, RA CMC

North Chicago, IL · On-site

$160K/yr

Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...

AbbVie

Director, RA CMC

North Chicago, IL

$144K - $190K/yr

Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...

AbbVie

Director, RA CMC

Irvine, CA

$161K - $212K/yr

Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...

AbbVie

Director, RA CMC

North Chicago, IL · On-site

$144K - $190K/yr

Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...

AbbVie

Director, RA CMC

Waltham, MA · On-site

$160K/yr

Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...

AbbVie

Director, RA CMC

North Chicago, IL

$144K - $190K/yr

Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...

AbbVie

Director, RA CMC

Irvine, CA · On-site

$160K/yr

Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...

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All JobsCmc Operations Jobs

Cmc Operations information

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$11

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$53

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.

CMC Regulatory Lead

Retro

Redwood City, CA • On-site

$200K - $240K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 19 days ago

Job description

Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan.
 
We're hiring an experienced CMC Regulatory Lead to own the strategy and operations for our Chemistry, Manufacturing, and Controls (CMC) regulatory work. As one of the earliest members of the Regulatory Affairs team, you will work across Retro's programs and play a leading role in building out the regulatory CMC capabilities and strategies to achieve our ambitious mission and tackle aging. You will report directly to the leader of Regulatory Affairs.
 
This position is an onsite role based in Redwood City.
 
About you:
You are a builder and doer who can set clear, global CMC regulatory strategies and roll up your sleeves to execute them at speed. You are energized by complex CMC challenges, especially in cell therapy, and you anticipate questions before they become risks. You translate technical details into clear regulatory narratives that resonate with health authorities, and you are comfortable serving as the CMC regulatory point person in high-stakes health-authority interactions.
 
You have high-collaboration and low-ego tendencies, with the ability to align cross-functional technical teams and external partners around a shared regulatory CMC plan and clear deliverables. You bring strong operational discipline, enjoy creating structure when needed, and are mission-driven with genuine motivation to advance longevity and aging biology for the benefit of humanity.
In this role, you will:
  • Be accountable for the regulatory CMC activities for Retro's programs, which include both cell therapies and small molecules.
  • Develop the regulatory CMC strategy for each program and lead the execution of global CMC regulatory plans.
  • Lead the preparation of the CMC dossier for INDs/CTAs and marketing applications, as well as the CMC documents for amendments, annual reports, and other CMC regulatory submissions.
  • Act as Retro's regulatory liaison with health authorities for CMC communications and submissions.
  • Lead health-authority meetings with FDA and other health authorities for CMC-related topics.
  • Lead the responses to health-authority queries and information requests related to CMC.
  • Identify regulatory CMC risks and develop creative and innovative mitigation strategies.
  • Partner closely with key internal functions, including Analytical Development, Process Development, Scientific Operations, and Quality.
  • Provide regulatory CMC guidance and oversight to external CDMOs and other vendors.
  • Help establish scalable regulatory CMC processes and approaches in a growing biotech organization.
You will thrive in this role if you:
  • 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 strategy for cell therapies.
  • Experience working in early phase development (IND/CTA-enabling through Phase 1/2) with pragmatic, stage-appropriate CMC approaches.
  • Proven ability to lead cross-functional workstreams, manage multiple priorities, and deliver high-quality outputs under tight timelines.
  • Strong interest in longevity and aging biology, and motivation to work in a field where the playbook is still being written.
It's a bonus if you:
  • Have experience working on iPSC-derived cell therapies.
  • Have experience across multiple product modalities (e.g., cell/gene therapy, small molecules, biologics, etc.).
  • Experience in late phase development (e.g., Phase 3) and registrational/commercial settings.
  • Extensive global experience, including in non-traditional jurisdictions and emerging markets. 
$200,000 - $240,000 a year
At Retro, we don't use titles. New hires join as a "Member of X Team." Depending on experience, this role is approximate to Director level.
 
Total compensation also includes generous equity and benefits including:
- Medical, dental, and vision insurance for you and your family
- 401(k) plan with 4% matching
- Unlimited time off and 10 company holidays per year
- Paid parental leave
- Annual learning & development stipend 
- Monthly longevity stipend
- Free lunch and snacks
We take pride in cultivating an environment that fosters collaboration, open communication, and authenticity. We believe that great results are best delivered by a highly creative team working in concert. We are an equal opportunity employer; we do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We are diverse in background and singular in mission.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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