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Cmc Auditor Jobs (NOW HIRING)

Socket.dev

Sr. Consultant, CMC

Virginia, MN · On-site

Senior Consultant, CMC Position Summary The Senior Consultant, CMC is a mid- to senior-level role ... Knowledge of Quality Management Systems and auditing for GMP in the manufacturing and QC ...

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Jobtailor

Senior Accounting Manager

San Francisco, CA · On-site

* Manage general accounting areas such as R&D and CMC accruals and other liabilities * Support the ... Support internal and external audits by preparing audit schedules and responding to auditor ...

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Latigo Biotherapeutics

Senior Accountant

San Francisco, CA · On-site

$87K - $109K/yr

Manage general accounting areas such as R&D and CMC accruals and other liabilities, among others ... Support internal and external audits by preparing audit schedules, responding to auditor requests ...

New

Latigo Bio

Senior Accountant

San Francisco, CA · On-site

$87K - $109K/yr

Manage general accounting areas such as R&D and CMC accruals and other liabilities, among others ... Support internal and external audits by preparing audit schedules, responding to auditor requests ...

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Cmc Auditor information

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How much do cmc auditor jobs pay per year?

As of Sep 13, 2026, the average yearly pay for cmc auditor in the United States is $72,633.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,000.00 and $98,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Cmc Auditor jobs?

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

Head of Chemistry, Manufacturing, and Controls (CMC)

Boston, MA • On-site

Voisin Consulting SARL
See more jobs at Voisin Consulting SARLexternal

Other

Re-posted 9 days ago

Job description

We are seeking an experienced and strategic Head of Chemistry, Manufacturing, and Controls (CMC) to lead the development and execution of global CMC strategy across a diverse therapeutic portfolio. This individual will provide technical and organizational leadership for biologics, combination products, oligonucleotides, and cell and gene therapy programs, spanning early development through late-stage development and commercialization readiness.

The successful candidate will combine deep drug development expertise, strong cross‑functional leadership, and proven experience building, managing, and developing teams. Consulting experience is a plus.

Key Responsibilities
  • Define and lead phase‑appropriate global CMC strategies across modalities for a diverse range of global clients
  • Provide thought leadership to raise the VCLS profile, including speaking at conferences, presenting webinars, and meeting VCLS clients
Technical Oversight
  • Enable our clients’ development of biologics, oligonucleotides, combination products, and cell & gene therapies
  • Guide scalable manufacturing and analytical strategies
  • Write and review technical documentation, and provide input and support for CMC team members
Regulatory Leadership
  • Oversee IND, CTA, BLA, NDA, MAA, and IMPD CMC documentation
  • Represent CMC in health authority interactions
Vendor Management
  • Manage external partners, including external auditing and consulting partners
  • Drive performance and issue resolution
People Leadership
  • Lead and develop a team of 5–10 staff
  • Build a high‑performing and collaborative culture
Cross‑functional Collaboration
  • Partner with Regulatory, non‑clinical, clinical, and business development teams to bring phase‑appropriate solutions to VCLS clients and build the VCLS business
Qualifications
  • Degree in a relevant scientific discipline
  • Significant industry experience in CMC and drug development
  • Expertise across biologics, oligonucleotides, combination products, and cell & gene therapies
  • Experience managing mid to large teams
  • Strong regulatory submission experience (US and/or UK/EU)
  • Knowledge of GMP and global regulatory requirements
  • Experience with CDMOs
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