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Cmc Technical Lead Jobs (NOW HIRING)

Pathos

Director, CMC - Biologics & ADC

New York, NY · On-site

$210K - $250K/yr

About the Role We are seeking a Director, CMC - Biologics & ADC to lead the chemistry ... This is a foundational hire on the Pathos CMC/Technical Operations team. You will help build and ...

Pathos

Director, CMC - Biologics & ADC

Manhattan, NY · On-site

About the Role We are seeking a Director, CMC - Biologics & ADC to lead the chemistry ... This is a foundational hire on the Pathos CMC/Technical Operations team. You will help build and ...

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Cmc Technical Lead information

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$30K

$156.3K

$206K

How much do cmc technical lead jobs pay per year?

As of Sep 11, 2026, the average yearly pay for cmc technical lead in the United States is $156,348.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,000.00 and $205,000.00 per year, depending on experience, location, and employer.

What is the difference between Cmc Technical Lead vs Cmc Project Manager?

AspectCmc Technical LeadCmc Project Manager
Primary FocusTechnical oversight and leadership of CMC activitiesProject planning, execution, and delivery management
Required CredentialsScientific or engineering degree, industry-specific certificationsProject management certifications (PMP), relevant degrees
Work EnvironmentLaboratories, manufacturing sites, R&D settingsOffice-based, cross-functional teams, client interactions
Industry UsagePharmaceutical, biotech, or life sciences companiesPharmaceutical, biotech, or life sciences companies

The Cmc Technical Lead primarily focuses on technical leadership within CMC functions, ensuring scientific and manufacturing processes meet quality standards. In contrast, the Cmc Project Manager oversees project timelines, budgets, and coordination across teams. Both roles are essential in the drug development process but serve different strategic purposes.

What are typical Cmc Technical Lead job responsibilities?

A CMC Technical Lead oversees the development, validation, and manufacturing processes related to chemistry, manufacturing, and controls for pharmaceutical products. They coordinate cross-functional teams, ensure compliance with regulatory standards, and review technical documentation. Strong knowledge of GMP regulations, project management skills, and experience with CMC development tools are essential for this role.

What states have the most Cmc Technical Lead jobs?

States with the most job openings for Cmc Technical Lead jobs include:

What are popular job titles related to Cmc Technical Lead jobs?

For Cmc Technical Lead jobs, the most frequently searched job titles are:

Infographic showing various Cmc Technical Lead job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 10% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $156,348 per year, or $75.2 per hour.

Manager, CMC Project Management

Waltham, MA

Crescent Biopharma
See more jobs at Crescent Biopharmaexternal

$140K - $180K/yr

Full-time

PTO

Re-posted 22 days ago

Job description

Crescent Biopharma's vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company's clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X.

We are seeking a Manager, CMC Project Management who is responsible for driving cross-functional execution of CMC activities in support of early and late-stage clinical development programs. Working closely with Technical Operations  - including Drug Substance, Drug Product, Analytical Development, Regulatory CMC, Quality, Supply Chain and external partners, this role leads integrated project planning, facilitates cross-functional alignment, manages risks and timelines, and enables successful delivery of CMC milestones in support of regulatory and development objectives. This role is based in Waltham, MA and you must have experience in the oncology space.

Responsibilities
  • Lead cross-functional CMC project management for clinical-stage development programs, developing and maintaining integrated project plans, timelines, critical path activities, milestones, risks, and decision logs.
  • Drive project execution by facilitating cross-functional meetings, tracking actions and decisions, proactively identifying risks and dependencies, and escalating issues to ensure program objectives are achieved.
  • Coordinate activities across Drug Substance, Drug Product, Analytical Development, Quality Control, Quality Assurance, Supply Chain, Regulatory CMC, and other Technical Operations functions to ensure alignment of priorities and deliverables
  • Partner with CDMOs, CROs, testing laboratories, and other external vendors to monitor deliverables, manufacturing activities, timelines, and issue resolution.
  • Coordinate planning and execution of CMC regulatory submissions, including INDs, IMPDs, amendments, and health authority responses, ensuring cross-functional deliverables are completed on schedule.
  • Support program budgeting, forecasting, resource planning, purchase order tracking, and financial reporting to enable effective execution of CMC development activities.
  • Identify and implement process improvements to strengthen CMC project execution, governance, resource planning, and organizational effectiveness.
Education & Experience
  • Bachelor's degree in a scientific, engineering, or related discipline required.
  • 5-8 years of biotech or pharmaceutical industry experience.
  • Experience in CMC, Technical Operations, Project Management, Manufacturing, Supply Chain, or related functions.
  • Familiarity with GMP manufacturing and external partner management.
  • Strong project management and organizational skills.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Excellent communication and collaboration skills.
  • Experience with project planning and tracking tools.
  • Ability to identify risks and drive issue resolution.
  • Detail-oriented with strong follow-through and accountability
What We Offer
  • Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment
  • Competitive compensation, including base salary, performance bonus, and equity
  • 100% employer-paid benefits package
  • Flexible PTO; also, two, one-week company-wide shutdowns each year
  • A commitment to your professional development, with access to resources, mentorship, and growth opportunities
$140,000 - $180,000 a year
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