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Cmc Project Jobs (NOW HIRING)

Avid Bioservices

Intern, CMC Project Management

Tustin, CA · On-site

$31.40K - $36.70K/yr

Description The Intern, CMC Project Management will support client facing program teams in the planning, coordination, and execution of Chemistry, Manufacturing & Controls (CMC) activities. Working ...

Avid Bioservices

Intern, CMC Project Management

Tustin, CA

$31.40K - $36.70K/yr

The Intern, CMC Project Management will support client facing program teams in the planning, coordination, and execution of Chemistry, Manufacturing & Controls (CMC) activities. Working closely with ...

Sanofi

Regulatory Affairs CMC Project Lead

Morristown, NJ · On-site +1

$154.30K - $203.70K/yr

Regulatory Affairs CMC Project Lead * Location: Morristown, NJ About the job As Regulatory Affairs CMC Project Lead within our R&D team , you will serve as a strategic regulatory expert who ...

Sanofi

Regulatory Affairs CMC Project Lead

Framingham, MA · On-site +1

$154.30K - $203.70K/yr

Regulatory Affairs CMC Project Lead * Location: Morristown, NJ About the job As Regulatory Affairs CMC Project Lead within our R&D team , you will serve as a strategic regulatory expert who ...

Sanofi

Regulatory Affairs CMC Project Lead

Morristown, NJ · On-site

$154.30K - $203.70K/yr

Regulatory Affairs CMC Project Lead * Location: Morristown, NJ About the job As Regulatory Affairs CMC Project Lead within our R&D team , you will serve as a strategic regulatory expert who ...

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Cmc Project information

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How much do cmc project jobs pay per hour?

As of May 30, 2026, the average hourly pay for cmc project in the United States is $21.55, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.28 per hour, depending on experience, location, and employer.

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

To thrive as a CMC (Chemistry, Manufacturing, and Controls) Project Manager, you need expertise in pharmaceutical development, regulatory requirements, and project management, often supported by a degree in life sciences or engineering. Familiarity with tools such as project management software (e.g., MS Project), quality management systems, and regulatory submission platforms is essential. Strong organizational skills, effective communication, and cross-functional leadership are critical soft skills for coordinating complex projects and teams. These abilities ensure that CMC projects meet regulatory standards, timelines, and quality objectives, leading to successful drug development and approval.

What are some common challenges faced by CMC Project Managers when coordinating cross-functional teams in pharmaceutical development?

CMC Project Managers often work with diverse teams, including scientists, regulatory specialists, and manufacturing experts, which can present challenges in aligning timelines, priorities, and communication styles. Navigating regulatory requirements while ensuring technical milestones are met requires strong organizational skills and proactive problem-solving. Effective CMC Project Managers facilitate clear communication, manage dependencies between functions, and adapt plans as project needs evolve, all while keeping the project on track for successful submissions.

What are CMC Project managers?

CMC Project managers oversee the Chemistry, Manufacturing, and Controls (CMC) aspects of drug development and production. They coordinate activities across various teams, ensuring that pharmaceutical products meet regulatory standards for quality, safety, and efficacy. Their responsibilities include managing timelines, budgets, documentation, and communication between research, manufacturing, and regulatory affairs. CMC Project managers play a critical role in bringing new drugs to market efficiently and compliantly.

What is the difference between Cmc Project vs Cmc Specialist?

AspectCmc ProjectCmc Specialist
CredentialsTypically requires a degree in life sciences or related field, with experience in project managementRequires a degree in chemistry, pharmacy, or related field, with knowledge of CMC regulations
Work EnvironmentInvolves managing cross-functional teams in pharmaceutical or biotech companiesFocuses on technical CMC activities, often within R&D or manufacturing settings
Industry UsageUsed in project planning, coordination, and oversight of CMC activitiesUsed in executing specific CMC tasks, data review, and regulatory submissions

The main difference is that a Cmc Project manages overall CMC activities and timelines, while a Cmc Specialist focuses on technical execution and data handling within those projects.

More about Cmc Project jobs
What are the most commonly searched types of Cmc Project jobs? The most popular types of Cmc Project jobs are:
What job categories do people searching Cmc Project jobs look for? The top searched job categories for Cmc Project jobs are:
Cmc Project jobs near you
Infographic showing various Cmc Project job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $44,814 per year, or $21.5 per hour.
Senior Director, CMC Project Management

Senior Director, CMC Project Management

Mirum Pharmaceuticals

Foster City, CA • Hybrid

$270K - $300K/yr

Other

Posted 29 days ago

Job description

POSITION SUMMARY

We are looking for a Senior Director of CMC Project Management who is upbeat, organized, self-motivated, collaborative, detail-oriented, and has a strong technical background and knowledge base.  The person filling this player/coach role will partner with the Head of Tech Ops, Biologics to provide strategic and operational leadership to the brelovitug CMC program, overseeing the development and implementation of integrated CMC plans from PPQ campaigns through global regulatory submission, approval, commercial launch, and lifecycle management activities. This role requires being able to prioritize to meet both short-term and long-term goals. This is a fantastic opportunity to make an impact, wear many hats, and be a part of an exciting growing biotech company.  This position is located in Foster City.

JOB FUNCTIONS/RESPONSIBILITIES

  • Manage program CMC budgets and related contracts, partnering with internal Finance and Contract functions.
  • Serve as the primary business lead for external partners, ensuring technical transfers,  manufacturing campaigns, testing, and other externally sourced activities stay on schedule and within budget.
  • Maintain dashboards and reporting mechanisms for program status, risks, decisions, and critical path updates for team and senior/executive leadership.
  • Facilitate cross-functional communications to gather inputs, align priorities, resolve conflicts, and share project updates; ensure clarity of owners, deliverables, and deadlines.
  • Maintain an integrated program timeline identifying critical decision points, governance reviews, team events, and key milestones.
  • Partner with Program Project Management to ensure appropriate integration with overall product strategy, timelines, and reporting, including alignment between development activities and portfolio-level planning as needed.
  • Support preparation for governance reviews and executive program presentations, ensuring materials are accurate, aligned, decision-oriented, and delivered on schedule.
  • Drive disciplined change control and documentation of scope/timeline changes, ensuring impacts are understood and communicated to stakeholders.

QUALIFICATIONS

Education /Experience:

  • Bachelor's degree; advanced degree (M.S., Ph.D, or MBA) preferred.
  • At least 15+ years of work experience in the pharmaceutical/biotech industry with a significant focus on CMC project management for biologics.
  • Experience managing relationships with biologics CDMOs.
  • Able to effectively communicate updates, issues, and strategic solutions to problems.
  • PMP (Project Management Professional) or equivalent accreditation is desired.

KNOWLEDGE, SKILLS, AND ABILITIES

  • Strong interpersonal skills and ability to collaborate across functions; proven ability to influence without authority.
  • Strong PM fundamentals (meeting management, timeline/critical path management, risk and issue management, decision tracking, action management, governance preparation).
  • Proactive, forward-thinking, and able to anticipate needs in dynamic environments with competing priorities.
  • Exceptional facilitation and communication skills (including executive-ready written and presentation skills) with success influencing at all levels cross-functionally.
  • Strategic, able to identify long term needs and risks and to incorporate these into a long-term plan. Proven ability to make smart business decisions while balancing scientific, technical, and risk-based factors.
  • Highly collaborative with outstanding relationship-building skills; ability to lead teams, navigate ambiguity, and resolve conflict effectively.
  • Experience with project/portfolio management tools and systems and strong working knowledge of common collaboration tools (e.g., MS Office, Smartsheet, SharePoint).
  • Willing to travel and to participate in teleconferences during non-business hours.

The salary range for this position is $270,000 to $300,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee's geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.

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