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Cmc Program Manager Jobs in Antioch, CA (NOW HIRING)

Cerus

Technical Operations Manager CMC

Concord, CA · On-site

$160K - $175K/yr

... Manager with expertise across Chemistry, Manufacturing, and Controls (CMC) activities supporting ... Lead stability programs for API and combination drug product. * Ensure compliance with FDA, EMA ...

New

Cerus

Technical Operations Manager CMC

Concord, CA · Hybrid

$160K - $175K/yr

... Manager with expertise across Chemistry, Manufacturing, and Controls (CMC) activities supporting ... Lead stability programs for API and combination drug product. * Ensure compliance with FDA, EMA ...

New

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All JobsCmc Program JobsCmc Program Manager JobsCmc Program Manager Jobs in Antioch, CA

Cmc Program Manager information

See Antioch, CA salary details

$43.8K

$122.2K

$178.5K

How much do cmc program manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for cmc program manager in Antioch, CA is $122,179.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,400.00 and $150,600.00 per year, depending on experience, location, and employer.

What is a CMC Program Manager?

CMC Program Managers are professionals responsible for overseeing the Chemistry, Manufacturing, and Controls (CMC) aspects of pharmaceutical or biotechnology product development. They coordinate cross-functional teams to ensure that drug development activities related to product formulation, manufacturing, quality, and regulatory submissions are completed on time and within budget. Their role is crucial in advancing products through clinical development to commercialization while ensuring compliance with global regulatory requirements.

What are the key skills and qualifications needed to thrive as a CMC Program Manager?

To thrive as a CMC Program Manager, you need expertise in chemistry, manufacturing, and controls (CMC), project management experience, and an advanced degree in life sciences or a related field. Familiarity with regulatory submission systems, quality management tools, and certifications such as PMP or Six Sigma are highly valued. Strong leadership, cross-functional communication, and problem-solving skills help manage diverse teams and complex projects effectively. These skills ensure the successful development, regulatory compliance, and timely delivery of pharmaceutical products.

What are some typical challenges a CMC Program Manager faces when coordinating cross-functional teams?

A CMC Program Manager often encounters challenges in aligning the goals and timelines of diverse teams such as process development, analytical, regulatory, and manufacturing. Communication gaps and shifting priorities can complicate project execution, especially when managing external partners or contract manufacturing organizations. Proactive stakeholder engagement and clear documentation are essential to ensure that everyone remains on track and regulatory requirements are met. Successfully navigating these complexities is key to advancing products efficiently through the development pipeline.

What is the difference between Cmc Program Manager vs Cmc Project Manager?

AspectCmc Program ManagerCmc Project Manager
CredentialsTypically requires a Bachelor's degree in life sciences, engineering, or related field; often certifications like PMP or PgMPUsually holds a Bachelor's degree in a relevant field; PMP certification is common
Work EnvironmentOversees multiple projects within a program, coordinating cross-project activities in biotech or pharma industriesManages individual projects, focusing on specific deliverables within the CMC scope
Employer & IndustryPharmaceutical, biotech, or life sciences companies managing complex product developmentSimilar industry, often within the same companies, focusing on specific project execution

The Cmc Program Manager oversees multiple related projects, ensuring alignment with strategic goals, while the Cmc Project Manager focuses on executing individual projects within the CMC domain. Both roles require similar credentials and work in the same industry, but differ in scope and responsibilities.

What job categories do people searching Cmc Program Manager jobs in Antioch, CA look for?

The top searched job categories for Cmc Program Manager jobs in Antioch, CA are:

What cities near Antioch, CA are hiring for Cmc Program Manager jobs?

Cities near Antioch, CA with the most Cmc Program Manager job openings:

Cmc Program Manager jobs near you
Infographic showing various Cmc Program Manager job openings in Antioch, CA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $122,179 per year, or $58.7 per hour.

Technical Operations Manager CMC

Cerus

Concord, CA • On-site

$160K - $175K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

New

Job description

About Cerus:
Cerus aims to be the global leader and trusted partner of blood centers and hospitals whose technology, services, and commitment are the lifeblood of safe and accessible blood for patients around the world.
This is a hybrid opportunity based out of Concord, CA where you'll work twice a week in the office.
Position Summary
Cerus is seeking an experienced Technical Operations Manager with expertise across Chemistry, Manufacturing, and Controls (CMC) activities supporting commercial and development-stage products. This role will serve as a key technical resource responsible for driving process development, process validation, technology transfer, manufacturing and analytical support, regulatory submissions, and lifecycle management activities across medical device, pharmaceutical, small and large molecule combination products.
The role will work closely with internal cross-functional teams, Cerus internal development and analytical laboratories, contract manufacturing organizations (CMOs) contract testing laboratories (CTLs), and regulatory partners to ensure successful execution of CMC programs. The individual will leverage internal laboratory capabilities where appropriate while coordinating and overseeing external partners to execute analytical development and testing, process development, technology transfer, validation, and manufacturing activities. The ideal candidate will possess deep expertise in pharmaceutical and/or medical device manufacturing, analytical sciences, regulatory compliance, process validation, and commercialization activities, with demonstrated success supporting global regulatory filings and product lifecycle management. In addition, the role will provide operational oversight for site activities including material management, shipping and receiving, inventory control, and equipment maintenance and coordination of internal and external technical resources to ensure efficient execution of development and manufacturing programs.
Primary Responsibilities
  • Provide technical expertise for development and commercial products.
  • Support process development, characterization, scale-up, analytical (development, release and stability testing) and commercialization activities internally and at CMOs.
  • Support manufacturing and analytical testing-related investigations
  • Manage change controls, deviations, CAPAs, and risk assessments.
  • Lead stability programs for API and combination drug product.
  • Ensure compliance with FDA, EMA, ICH, USP, ISO, and ASTM requirements.
  • Author and review technical documentation, specifications, protocols, and reports.
  • Author, review, interpret data for CMC sections for global regulatory submissions.
  • Collaborate with RA, QA, Supply Chain, Manufacturing, and R&D teams.
  • Manage shipping and receiving activities for clinical and development materials, ensuring compliance with applicable quality and regulatory requirements.
  • Coordinate inventory management activities, including tracking of raw materials, components, consumables, reference standards, and development samples.

Qualifications
  • B.S or M.S. in, Pharmaceutical Sciences, Chemistry, Biomedical Engineering, or related scientific discipline preferred.
  • 10 years of experience in pharmaceutical, biotechnology, medical device, or combination product industries with a minimum of 5 years experience with CMC development, process validation, analytical development and validation, stability management, tech transfer, change controls, and regulatory submissions preferred
  • Demonstrated success managing CMOs and cross-functional project teams.
  • Excellent technical writing, communication, and project management skills.
  • AI-enabled process and analytical development and manufacturing optimization is a plus.
Travel
Up to 15% domestic and international travel as required.
We understand that our people are essential to our success. This philosophy is revealed in our competitive benefits package, designed to improve employees' lives both on and off the job.
Benefits plans: medical, dental, vision, domestic partner benefits, paid maternity and paternity leaves, healthcare and dependent care flexible spending, life and accidental death insurance, long-term and short-term disability insurance, matching 401(k), RSUs
Work and family: EAP, legal and financial services, health club membership discounts, tuition reimbursement
Compensation: The base salary range for this position in the selected city is $160,000-$175,000 annually. Base pay is one part of the total package to compensate and recognize employees for their work.
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About Cerus

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

201 - 500 Employees

Headquarters location

Concord, CA, US

Year founded

1991

Social media

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