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From Home Cmc Consultant Jobs (NOW HIRING)

Atomic

CMC Consultant

Indomo is a clinical stage therapeutics company transforming clinic-based procedures into at-home ... Experience supporting programs from early clinical through late-stage development. Why Join Indomo:

ZS

Decision Analytics Consultant- CMC

Manhattan, NY · On-site

$160K - $177K/yr

As a management consulting and technology firm focused on improving life and how we live it, we ... A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS ...

Accenture

Travel is required for this role and could vary from 0-75%. HERE'S WHAT YOU'LL NEED: * Minimum ... consulting or industry in life sciences supply chain and manufacturing space in digital CMC and PLM

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From Home Cmc Consultant information

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How much do from home cmc consultant jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for from home cmc consultant in the United States is $49.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $62.50 per hour, depending on experience, location, and employer.

What is a from home CMC consultant?

From Home CMC (Chemistry, Manufacturing, and Controls) Consultants are professionals who provide expert advice and guidance on the development, manufacturing, and regulatory compliance of pharmaceutical products, all while working remotely. They assist companies in preparing CMC documentation for regulatory submissions, ensuring product quality, and developing efficient manufacturing processes. These consultants leverage their specialized knowledge to help organizations meet industry standards and regulatory requirements without being physically present at a client's site.

What skills and qualifications are needed to thrive as a from home CMC consultant?

To thrive as a From Home CMC (Chemistry, Manufacturing, and Controls) Consultant, a solid background in pharmaceutical sciences, regulatory affairs, and CMC documentation is essential, usually supported by a relevant science degree and industry experience. Familiarity with regulatory submission tools (such as eCTD), quality management systems, and databases like TrackWise is typically required. Strong project management, communication, and problem-solving abilities help consultants effectively liaise with clients and regulatory bodies remotely. These competencies ensure accurate regulatory submissions, compliance, and successful project outcomes in a virtual consulting environment.

What are common challenges faced by a from home CMC consultant and how can they be addressed?

As a remote CMC (Chemistry, Manufacturing, and Controls) Consultant, one common challenge is maintaining effective communication with clients and cross-functional teams spread across different locations and time zones. It’s important to establish clear communication channels, set regular check-in meetings, and use collaboration tools to stay aligned on project goals and regulatory timelines. Another challenge is accessing and reviewing confidential documents securely, which can be managed by using company-approved secure file-sharing platforms and adhering to strict data privacy protocols. Staying proactive and organized helps ensure smooth project execution and client satisfaction.

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

AspectFrom Home Cmc ConsultantFrom Home Regulatory Affairs Specialist
CredentialsBachelor's degree in life sciences, chemistry, or related field; industry certificationsBachelor's degree in life sciences, pharmacy, or related; regulatory certifications often preferred
Work EnvironmentRemote, project-based consulting for pharmaceutical companiesRemote or office-based, focusing on compliance and submissions
Industry UsageConsulting firms, pharmaceutical companies, biotechPharmaceutical, biotech, medical device companies
Common Search/ComparisonYesYes

While both roles involve working remotely in the pharmaceutical industry, From Home Cmc Consultants focus on product development, formulation, and manufacturing processes, providing expert advice. In contrast, From Home Regulatory Affairs Specialists handle compliance, submissions, and regulatory documentation to ensure products meet legal standards. Both require similar educational backgrounds and certifications but serve different functions within the industry.

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From Home Cmc Consultant jobs near you
Infographic showing various From Home Cmc Consultant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, and 3% Contract. Highlights an 71% Physical, 1% Hybrid, and 28% Remote job distribution, with an average salary of $103,425 per year, or $49.7 per hour.

CMC Consultant

Atomic

Remote

Contractor

Re-posted 3 days ago

Job description

About Us:
Indomo is a clinical stage therapeutics company transforming clinic-based procedures into at-home care via device-enabled therapeutics. Indomo's lead program couples a proven corticosteroid with an innovative intradermal self-injection device to create the first fast-acting at-home solution for inflammatory acne lesions.
Position Overview:
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 advancing our lead asset through the NDA pathway by guiding CMC development, managing external partners, and ensuring regulatory readiness.
This role is ideal for a senior CMC expert who thrives in a hands-on, advisory + execution capacity and is comfortable working closely with a lean internal team and external CDMOs. The consultant will provide both strategic direction and tactical oversight across drug product development, analytical strategy, and integration with our device-enabled delivery system.
Key Responsibilities:
CMC Strategy
  • Help define and execute the overall CMC development strategy to support clinical progression and trial readiness
  • Support outsourced drug substance and drug product development with CDMO, including formulation optimization, stability, and device compatibility
  • Establish critical quality attributes, specifications, and acceptance criteria
  • Guide analytical method development, validation, and lifecycle management

External Vendor & Manufacturing Oversight
  • Interface with external stakeholders, including CDMOs, CROs, and suppliers.
  • Support selection, onboarding, and management of external partners.
  • Review deliverables, ensure timelines are met, and mitigate technical risks.
  • Advise on quality systems and inspection readiness.

Regulatory Support
  • Partner with regulatory team to shape CMC strategy for IND submission.
  • Organize execution of and contribute to regulatory documents (IND, briefing packages, NDA modules).
  • Prepare for and support FDA interactions (e.g., IND, EOP2, Type C meetings).

Qualifications:
Required
  • Advanced degree (Ph.D. preferred) in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field.
  • 10+ years of drug development experience with demonstrated leadership of CMC strategy in biotech/pharmaceutical settings.
  • Expertise in formulation development, analytical method development/validation, stability programs, GMP manufacturing, and quality compliance.
  • Strong knowledge of FDA regulations, GMP guidelines, and global regulatory requirements.
  • Strong track record supporting INDs and/or NDAs.
  • Ability to operate independently in a fast-paced, dynamic startup environment.

Preferred
  • Experience with combination products (drug + delivery device).
  • Successful prior interactions with FDA on CMC topics.
  • Experience supporting programs from early clinical through late-stage development.

Why Join Indomo:
  • Opportunity to shape CMC strategy for an innovative combination product.
  • High-impact role with direct access to leadership and decision-making.
  • Collaborative, mission-driven team.
  • Flexibility in working style and scope.

We are focused on building a diverse and inclusive workforce. If you're excited about this role, but do not meet 100% of the qualifications listed above, we encourage you to apply.
Atomic is an Equal Opportunity Employer and considers applicants for employment without regard to race, color, religion, sex, orientation, national origin, age, disability, genetics or any other basis forbidden under federal, state, or local law.
Please review our CCPA policies here.

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