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Resilience

Biologics and sterile injectables CDMO

Claims Specialist

Claims AdjudicationConfirmed live in the last 24 hours
Full-timeRemote in USA$130k - $150kRemote

About the Job

Requirements

  • Five years of experience in claims handling, claims advocacy, or cyber insurance coverage.
  • Ability to evaluate primary and excess coverage, manage increasingly complex cases, and communicate clearly with insureds, brokers, vendors, and underwriters.
  • Expertise handling third-party claims, particularly Technology Errors & Omissions and Miscellaneous Professional Lines.
  • Established connections within the cyber broking community, incident response, or cybersecurity sectors.

Responsibilities

  • Own the day-to-day investigation and management of Cyber, Technology Errors & Omissions, and Miscellaneous Professional Lines claims.
  • Conduct investigations, manage negotiations, and use insurance-contract expertise to recommend accurate claim reserves.
  • Collaborate with internal security and technology teams to provide policyholders with incident response and preventative services.
  • Manage external service providers during incidents to reduce losses.
  • Maintain meticulous claim-file documentation.
  • Establish a data and analytics feedback loop with the Underwriting team to refine risk selection.

About the Company

Resilience

Biologics and sterile injectables CDMO

Resilience is a North American CDMO focused on biologics and sterile drug products. It provides end-to-end services from development through commercial production, including biologics development and drug substance manufacturing, aseptic fill/finish, device assembly, packaging, logistics, regulatory support, and tech transfer, all coordinated via a stage-gate process and a digital quality management system. It differentiates itself with North American-based, integrated biologics and sterile capabilities, a focus on sterile injectables and device assembly, and recent expansion into injectable pen devices for diabetes and obesity medicines. Its goal is to broaden access to complex medicines while protecting North American biopharma supply chains with dependable capacity and strong regulatory support from clinical development to commercial scale.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$3.2B
Headquarters
Blue Ash, OH
Founded
2020

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