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Cmc Analytical Remote Jobs (NOW HIRING)

Allucent

Sr. Director, CMC

Cary, NC · Remote

We are looking for a Sr. Director, CMC to join our A-team (hybrid*/remote) in the USA. As a Sr. ... Lead end-to-end CMC strategy across drug substance, drug product, and analytical development--from ...

Allucent

Sr. Director, CMC

Cary, NC · On-site +1

We are looking for a Sr. Director, CMC to join our A-team (hybrid*/remote) in the USA. As a Sr. ... Lead end-to-end CMC strategy across drug substance, drug product, and analytical development-from ...

Allucent

Sr. Director, CMC

Cary, NC · Remote

We are looking for a Sr. Director, CMC to join our A-team (hybrid*/remote) in the USA. As a Sr. ... Lead end-to-end CMC strategy across drug substance, drug product, and analytical development-from ...

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$29.5K

$100.7K

$193.5K

How much do cmc analytical remote jobs pay per year?

As of Jun 7, 2026, the average yearly pay for cmc analytical remote in the United States is $100,673.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,500.00 and $125,000.00 per year, depending on experience, location, and employer.

What is a CMC Analytical Remote role?

A CMC Analytical Remote role involves supporting Chemistry, Manufacturing, and Controls (CMC) activities related to analytical testing and data review, but performed remotely rather than on-site. Professionals in this position are responsible for overseeing analytical method development, validation, and troubleshooting for pharmaceutical products. They often collaborate with cross-functional teams, review analytical data, ensure compliance with regulatory standards, and provide technical guidance, all while working from a remote location. This role is vital for ensuring product quality and regulatory submission readiness in the drug development process.

What are the key skills and qualifications needed to thrive as a CMC Analytical professional in a remote role, and why are they important?

To thrive as a CMC Analytical professional, you need expertise in analytical chemistry, method development, and regulatory compliance, typically supported by a degree in chemistry or related fields. Familiarity with chromatographic techniques (e.g., HPLC, GC), data analysis software, and regulatory documentation systems is essential. Strong attention to detail, problem-solving abilities, and effective remote communication skills help you excel in this position. These competencies are crucial for ensuring product quality, regulatory approval, and efficient collaboration in a distributed work environment.

What is the difference between Cmc Analytical Remote vs Cmc Analytical in-office?

AspectCmc Analytical RemoteCmc Analytical In-office
Work EnvironmentRemote, home-based setup with virtual collaborationOn-site laboratory or office environment
Required CredentialsLikely similar certifications in analytical chemistry or related fieldsSame certifications as remote role, with possible additional on-site training
Employer & Industry UsageUsed by companies offering remote analytical services or consultingTraditional laboratory or corporate settings in the industry
Work FlexibilityHigh flexibility in location and scheduleStandard office hours and location-based work

In summary, Cmc Analytical Remote roles offer flexibility and work-from-home options, while Cmc Analytical in-office positions involve on-site work. Both roles typically require similar credentials and serve the same industry, but differ mainly in work environment and scheduling.

How does a remote CMC Analytical professional typically collaborate with cross-functional teams to support drug development projects?

As a remote CMC Analytical professional, you’ll regularly interact with multidisciplinary teams such as formulation scientists, process engineers, and regulatory affairs. Collaboration usually happens through video meetings, shared project management tools, and cloud-based data analysis platforms. Clear communication and proactive updates are essential, as you’ll often provide analytical data to support decision-making in formulation and process development. While remote, you may also coordinate sample shipments and manage data review cycles to keep projects on track. This virtual teamwork structure helps ensure analytical activities align with overall project timelines and regulatory requirements.

Which job is best for work from home?

For a CMC Analytical role, remote work is common in positions such as laboratory scientists, quality assurance specialists, and regulatory affairs professionals, often requiring skills in data analysis, documentation, and familiarity with laboratory software. These roles typically involve tasks that can be performed using computers and communication tools from home, with some positions requiring periodic on-site visits or certifications. The suitability for remote work depends on the company's policies and the specific responsibilities of the role.
Infographic showing various Cmc Analytical Remote job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $100,673 per year, or $48.4 per hour.
Remote Analytical SME & CMC Technical Writer

Remote Analytical SME & CMC Technical Writer

Sigma Systems, Inc.

Ridgefield, CT • On-site, Remote

Full-time

Posted 4 days ago

Job description

37278373 Remote Analytical SME & CMC Technical Writer, 12 Months
Sigma Systems is seeking an Analytical SME & CMC Technical Writer to work remote

We are seeking an experienced Analytical Subject Matter Expert (SME) and CMC Technical Writer to support external drug substance (DS) and drug product (DP) development programs within External Alternative CMC development (EACD) at Boehringer Ingelheim.
This contract role combines deep expertise in DS/DP analytical development and quality control to support ongoing DS/DP external CMC development and demonstrated familiarity of Veera RIM system and technical writing capabilities to support documentation and global regulatory submissions (e.g., IND, CTA, NDA/MAA).
The successful candidate will collaborate with internal cross-functional teams and external partners (CDMOs/CROs) to ensure scientifically robust analytical strategies and clear, compliant CMC documentation aligned with global regulatory expectations.

Responsibilities:
Analytical Expertise

  • Provide scientific leadership in phase appropriate external DS/DP analytical development/QC for NCE and NCE-like (e.g., Oligonucleotide) entities, including method development, validation, transfer and lifecycle management
  • Contribute to development of DS/DP phase appropriate specifications and analytical control strategies in collaboration with internal and external teams
  • Contribute to development of DS/DP stability programs and assignment of DS retest period, DP shelf life and material holding times as needed, with internal and external teams to support FIH and following clinical trials
  • Independently propose or review quality agreement, SOW, study protocols/reports, batch/stability data, to support CMC deliverables in a timeline fashion.
  • Prepare and communicate clearly and independently technical plans, updates and deliverables as needed in the form of reports and/or presentations within the internal teams
  • Partner with internal teams and external vendors (CDMOs/CROs) to resolve technical challenges and quality events and ensure timely, compliant deliverables

CMC Technical Writing

  • Support departmental submission activities by managing documentation workflow workflow in Veeva RIM system
  • Demonstrated working experience in authoring, reviewing and editing (content and format) CTD Module 3 (Drug Substance and Drug Product) documents, in particular analytical related documents.
  • Contribute to preparation of regulatory submissions/briefings and responses to health authority inquirie

Requirements:

  • Advanced degree (e.g., PhD) is preferred, or Master's and Bachelor's degree in Analytical Chemistry, Pharmaceutical Sciences, or related discipline
  • Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development of NCE and NCE-like drug substance and solid and liquid formulations.
  • Demonstrated working experience in regulatory submissions
  • Familiarity with GMP and regulatory guidelines (e.g., ICH, FDA, EMA, USP, EP, etc.)

Preferred

  • Experience in global regulatory submissions (IND, CTA, NDA, MAA)
  • Experience working with external manufacturing or testing partners

Key Skills

  • Strong organization and technical writing skills
  • High attention to detail and scientific rigor
  • Effective communication and stakeholder collaboration
  • Ability to manage multiple priorities in a fast-paced environment