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Cmc Consultant Jobs (NOW HIRING)

Immatics NV

Senior CMC Program Manager

Houston, TX

$110K - $111K/yr

Experience coordinating external vendors, CMOs, CDMOs, or consulting partners * Strong ... Manage CMC deliverables, milestones, and critical paths while ensuring alignment with overarching ...

Argenx

Director, Regulatory CMC Device Leader

Boston, MA · On-site

$163K - $215K/yr

... consultants etc.) to ensure Reg CMC alignment and to integrate the global device strategy into submissions * Ensures goals are met, processes are aligned to ensure efficiencies and to promote ...

Immatics NV

Senior CMC Program Manager

Houston, TX · On-site

$110K - $111K/yr

Experience coordinating external vendors, CMOs, CDMOs, or consulting partners * Strong ... Manage CMC deliverables, milestones, and critical paths while ensuring alignment with overarching ...

Amoria Group

Sales Consultant

Dallas, TX · On-site

$85K - $100K/yr

As an Associate Consultant at CMC, you'll develop core sales skills including relationship building, negotiation, and business development. You'll start by focusing on candidate sourcing and, as you ...

Amoria Group

Sales Consultant

Dallas, TX

$85K - $100K/yr

As an Associate Consultant at CMC, you'll develop core sales skills including relationship building, negotiation, and business development. You'll start by focusing on candidate sourcing and, as you ...

Actalent

Senior Manager Of CMC Regulatory

Morristown, NJ · On-site

$140K - $165K/yr

Senior Manager CMC Regulatory A Partner to Actalent is seeking an experienced Manager of CMC ... With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada ...

CMC Phoenix

Overnight Pharmacist

Phoenix, AZ

$61 - $64/hr

College Medical Center Phoenix (CMC Phoenix) is seeking a full-time Pharmacist to join our team and ... Provide medication therapy consultations and support to healthcare staff and patients. * Document ...

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Cmc Consultant information

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$10

$38

$82

How much do cmc consultant jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for cmc consultant in the United States is $38.02, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $48.08 per hour, depending on experience, location, and employer.

What does a CMC specialist do?

A CMC (Chemistry, Manufacturing, and Controls) specialist is responsible for ensuring that pharmaceutical products meet regulatory standards throughout development and manufacturing. They prepare documentation, oversee quality processes, and collaborate with regulatory agencies to support product approval. Strong knowledge of GMP, regulatory guidelines, and laboratory practices is essential for this role.

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

To thrive as a CMC Consultant, you need a deep understanding of Chemistry, Manufacturing, and Controls (CMC) regulations, pharmaceutical development, and quality assurance, often supported by an advanced degree in life sciences or a related field. Familiarity with regulatory submission systems, GMP compliance tools, and relevant documentation software is typically required. Strong project management, analytical thinking, and effective communication skills help you collaborate with cross-functional teams and interpret complex regulatory requirements. These skills ensure successful regulatory submissions, product quality, and compliance throughout the drug development lifecycle.

How does a CMC Consultant typically interact with cross-functional teams during a project?

As a CMC (Chemistry, Manufacturing, and Controls) Consultant, you'll frequently collaborate with cross-functional teams such as regulatory affairs, quality assurance, and product development. Your role involves translating technical manufacturing and analytical requirements into documentation that meets regulatory standards, while also ensuring alignment with project timelines and goals. Regular meetings, written reports, and collaborative problem-solving are integral parts of daily responsibilities, helping to ensure seamless communication and efficient progress toward regulatory submissions and product launches.

What are CMC consultants?

CMC consultants are professionals who specialize in Chemistry, Manufacturing, and Controls (CMC) within the pharmaceutical, biotechnology, and related industries. Their primary role is to provide expert guidance on the development, manufacturing, and regulatory submission of drug products, ensuring compliance with international standards. They assist companies in preparing CMC documentation for regulatory agencies, troubleshooting manufacturing issues, and optimizing processes for quality and efficiency. CMC consultants often work on projects involving drug formulation, process validation, analytical method development, and quality control. Their expertise is crucial for bringing safe and effective therapies to market.

Is 30 too old to get into consulting?

Cmc Consultants, like many consulting roles, value experience and skills over age, and individuals can successfully enter the field at 30 or older. Relevant skills such as problem-solving, communication, and industry knowledge, along with certifications like PMP or MBA, can enhance prospects regardless of age.

What does a CMC consultant do?

A CMC (Chemistry, Manufacturing, and Controls) consultant provides expertise in pharmaceutical development, focusing on ensuring that drug products meet regulatory standards. They assist with documentation, process validation, and compliance for regulatory submissions, often working with teams to prepare for inspections and audits. Strong knowledge of GMP regulations and regulatory guidelines is essential for this role.

What is the highest paid consultant job?

Cmc consultants, specializing in chemistry, manufacturing, and controls for pharmaceutical and biotech industries, can earn high salaries, especially with extensive experience and advanced certifications. Senior-level consultants or those working in highly regulated or specialized fields often have the highest compensation, which can exceed six figures annually.

What is the difference between Cmc Consultant vs Regulatory Affairs Specialist?

AspectCmc ConsultantRegulatory Affairs Specialist
Required CredentialsBachelor's degree in life sciences, often with certifications in CMC or related fieldsBachelor's degree in life sciences, with certifications in regulatory affairs or compliance
Work EnvironmentConsulting firms, pharmaceutical or biotech companies, project-based rolesIn-house regulatory departments, pharmaceutical companies, government agencies
Industry UsageCommonly hired for CMC-related projects, product development, and compliance consultingResponsible for ensuring regulatory compliance, submissions, and communication with authorities

The main difference between a Cmc Consultant and a Regulatory Affairs Specialist lies in their focus and work setting. Cmc Consultants typically work on product development and compliance projects within consulting firms or client companies, while Regulatory Affairs Specialists handle ongoing regulatory submissions and compliance within organizations. Both roles require similar educational backgrounds but differ in scope and daily responsibilities.

More about Cmc Consultant jobs
What cities are hiring for Cmc Consultant jobs? Cities with the most Cmc Consultant job openings:
What are the most commonly searched types of Cmc Consultant jobs? The most popular types of Cmc Consultant jobs are:
What job categories do people searching Cmc Consultant jobs look for? The top searched job categories for Cmc Consultant jobs are:
Cmc Consultant jobs near you
Infographic showing various Cmc Consultant job openings in the United States as of June 2026, with employment types broken down into 25% Locum Tenens, 23% Full Time, 51% Part Time, and 1% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $79,074 per year, or $38 per hour.
Vice President, Global CMC Regulatory

Vice President, Global CMC Regulatory

Revolution Medicines

Redwood City, CA • On-site

$183K - $242K/yr

Full-time

Posted 11 days ago

Job description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
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

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$294,000-$367,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

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