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Vp Technical Operation Cmc Jobs (NOW HIRING)

Stackinfra

Vice President, Technical Operations

Plano, TX · On-site

$216K - $249K/yr

STACK is looking for a Vice President of Technical Operations to support all data centers across ... equipment/system operation * Demonstrate technical knowledge and experience in data center ...

Stackinfra

Vice President, Technical Operations

Denver, CO · On-site +1

$216K - $249K/yr

STACK is looking for a Vice President of Technical Operations to support all data centers across ... equipment/system operation * Demonstrate technical knowledge and experience in data center ...

Korsana Biosciences, Inc.

VP, CMC

Waltham, MA · On-site

$250/hr

VP, CMC Korsana Biosciences, Inc. Waltham, Massachusetts, United States About this positionAbout Us ... Provide technical leadership and oversee biologics product development, scale-up and tech transfer ...

Korsana Biosciences, Inc.

VP, CMC

Waltham, MA · On-site

$300K - $340K/yr

Position Overview The Vice President of CMC (Chemistry, Manufacturing, and Control) at Korsana ... Provide technical leadership and oversee biologics product development, scale-up and tech transfer ...

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Vp Technical Operation Cmc information

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How much do vp technical operation cmc jobs pay per year?

As of Sep 9, 2026, the average yearly pay for vp technical operation cmc in the United States is $145,590.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,500.00 and $187,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Vp Technical Operation Cmc jobs?

For Vp Technical Operation Cmc jobs, the most frequently searched job titles are:

VP, Technical Operations

Waltham, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$250/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago

Job description

Summary

The Vice President, Technical Operations will lead end-to-end CMC Technical Operations strategy across Drug Substance, Drug Product, and CMC Program Management, advancing small-molecule products from candidate selection and IND-enabling development through clinical development, registration, validation, commercial launch, ongoing manufacturing, and lifecycle management.

Responsibilities
  • Lead and develop Technical Operations and CMC Program Management; integrate/prioritize/execute Drug Substance, Drug Product, and cross-functional CMC activities across the product lifecycle.
  • Develop and execute phase-appropriate CMC strategies (Drug Substance, Drug Product, analytical development, manufacturing, controls, stability, validation, regulatory CMC, supply) from IND-enabling through registration, commercialization, and post-approval lifecycle management.
  • Provide technical leadership for small-molecule Drug Product development (formulation/process development, scale-up, technology transfer, characterization, control strategy, validation/PPQ, commercial readiness).
  • Provide oversight for Drug Substance development/manufacturing (scale-up, technology transfer, validation, control strategy, commercial readiness, lifecycle support).
  • Ensure CMC Program Management across the portfolio (deliverables, dependencies, critical paths, risks, resources, budgets, governance, decisions).
  • Oversee CDMOs/external manufacturing partners for development, validation, and clinical/commercial manufacturing.
  • Lead commercial manufacturing and lifecycle management (investigations, CAPAs, change controls, improvements, site transfers, continued process verification, supply continuity).
  • Partner with Supply Chain, Regulatory Affairs, Quality, and Program leadership to meet FDA/ICH/global regulatory and cGMP expectations.
  • Represent Technical Operations in cross-functional teams, executive governance, due diligence, portfolio planning, and risk management.
  • Manage resources, operating plans, budgets, and portfolio priorities.
Qualifications
  • MS/Ph.D. in Pharmaceutics/Pharmaceutical Sciences/Chemical Engineering/Chemistry (or related) with progressive pharmaceutical industry experience for a VP-level role.
  • Extensive small-molecule development/manufacturing experience; deep Drug Product expertise (formulation/process development, scale-up, technology transfer, characterization, control strategy, validation/PPQ, regulatory approval, commercial launch, ongoing manufacturing), including leading PPQ/commercial validation at external sites.
  • Broad Drug Substance technical knowledge to lead and challenge an experienced organization.
  • Demonstrated end-to-end CMC strategy development and integration across Drug Substance, Drug Product, analytical, regulatory, quality, manufacturing, and supply.
  • Strong CMC program/portfolio management (risks, dependencies, resources, budgets, timelines, governance, executive decision support).
  • Significant CDMO/external manufacturing partner management experience.
  • Strong cGMP and FDA/ICH/global regulatory knowledge; experience supporting INDs, NDAs, and post-approval submissions.
  • Ability to lead multidisciplinary technical teams and influence senior stakeholders.
  • Small-molecule Drug Product development across multiple dosage forms (oral solids and liquids).
  • Commercial lifecycle management and global manufacturing network experience (post-approval changes, site transfers, optimization, supply risk, international submissions).
  • Technical due diligence experience for licensing/acquisitions/partnerships.
Compensation and Benefits
  • Targeted Base Salary: $291,349 USD - $359,902 USD.
  • Additional benefits include health care, vision, dental, retirement, PTO, etc.
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