M5
jf_chemistry_manufacturing_controls_cmc::M5
Director, Chemistry, Manufacturing & Controls

Director, Chemistry, Manufacturing & Controls

manufacturingChemistry, Manufacturing & Controls (CMC) · M5 — M5 — Senior Director · Management

Directs CMC strategy and leads teams responsible for manufacturing processes, analytical controls, and regulatory compliance across a product portfolio.

Median pay · United States · annual

$194,360 USD

+120% vs M1 on this ladder

Typical range ()

$142,769$264,593

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5 of 8

Track

Management

11-0000

manufacturing

Coordinates

3 / 4 spaces

pay@2 · 2026-07

What this role is

Directs CMC strategy and leads teams responsible for manufacturing processes, analytical controls, and regulatory compliance across a product portfolio. At the Senior Director (M5) level, the role owns multiple functions or a large department, org-level trade-offs and investment, and drives multi-function results. Leads directors and managers.

What this level does

  • Directs the CMC organization through department managers, impacting division-wide development and commercial manufacturing operations
  • Defines the methods and standards for CMC regulatory strategy across the full development lifecycle, including post-approval lifecycle management
  • Influences executives and major regulatory-agency counterparts on complex, org-wide CMC issues and precedent-setting negotiations
  • Builds and partners with a network of subject matter experts across diverse CMC product development areas to strengthen organizational capability
Knowledge applied
Defines org-wide CMC methods and regulatory-strategy standards across the full development lifecycle and post-approval management.
Complexity & problem solving
Tackles complex, division-wide CMC problems, defining approaches with business-wide implications.
Collaboration & interaction
Influences executives and major regulatory-agency counterparts on key strategic issues and builds SME networks.
Typical experience
10–12+ years including second-level management and CMC strategy work.

Skills at this level

Core laboratory chemistry
Directs synthesis and purification of drug substances and applies organic chemistry and chemical-safety knowledge to govern bench execution and troubleshooting.
CMC regulatory strategy
Develops and manages content strategy for CMC submissions — INDs/CTAs and amendments, marketing applications, and supplements/variations — to enable first-pass health-authority approvals.
Technology transfer and manufacturing scale-up
Leads transfer of drug substance and drug product processes from development into scaled manufacturing, ensuring readiness across upstream and downstream operations.
Statistical and trend analysis
Uses statistical and trend analysis of process, stability, and analytical data to resolve OOS, OOT, stability, and manufacturing issues.
Health authority interaction
Plans and manages regulatory agency interactions — responding to health authority questions and negotiating CMC positions during submission review.
Global regulatory strategy
Manages global CMC regulatory strategy, agency negotiations, and corporate policy at senior and executive levels.
Cross-functional collaboration
Works across regulatory affairs, quality assurance, and manufacturing to align CMC deliverables and ensure product integrity.
Full development lifecycle CMC input
Provides strategic CMC guidance from early development through Phase 2b–3 pivotal studies, BLA/NDA submissions, and post-approval lifecycle management.
CMC practice development and business growth
Builds the CMC service offering through business development, team building, and market-visibility activities at industry and client events.
Budget and resource ownership
Owns CMC departmental budgets and vendor/resource allocation, shifting toward strategic vendor selection as scope grows.

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As of · 2026-07-30

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