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Evp Technical Operation Jobs (NOW HIRING)

Scorpion Therapeutics

VP, Technical Operations

Waltham, MA · On-site

$291K - $359K/yr

Represent Technical Operations in cross-functional teams, executive governance, due diligence ... for a VP-level role. * Extensive small-molecule development/manufacturing experience; deep Drug ...

Stackinfra

Vice President, Technical Operations

Plano, TX · On-site

$216K - $249K/yr

... equipment/system operation * Demonstrate technical knowledge and experience in data center ... Proven ability to influence executive stakeholders and lead through collaboration across complex ...

Stackinfra

Vice President, Technical Operations

Denver, CO · On-site +1

$216K - $249K/yr

... equipment/system operation * Demonstrate technical knowledge and experience in data center ... Proven ability to influence executive stakeholders and lead through collaboration across complex ...

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As of Sep 9, 2026, the average yearly pay for evp technical operation in the United States is $152,287.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,500.00 and $181,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Evp Technical Operation job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 6% Part Time, 4% Contract, and 1% Nights. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $152,287 per year, or $73.2 per hour.

VP, Technical Operations

Waltham, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$291K - $359K/yr

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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