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Resilience

Biologics and sterile injectables CDMO

Quality Assurance Associate 2

Regulatory & Quality (Life Sciences)Posted on Nov 13
Full-timeBlue Ash, OH, USA

About the Job

Requirements

  • Experience in the pharmaceutical industry, an operations environment, or Quality Assurance.
  • Strong ability and motivation to learn.

Responsibilities

  • Maintain an understanding of relevant production processes and quality systems.
  • Perform Quality Assurance review and approval of Good Manufacturing Practice documentation, including change requests, batch records and associated documentation, product and component release transactions in SAP, quality investigations involving deviations and product complaints, validation plans, protocols and reports, and standard operating procedures.
  • Collaborate with Quality professionals across the organization to ensure consistent application and execution of key quality systems.
  • Execute Quality Assurance processes, including batch record review, product disposition, and quality issue resolution, to maintain product and document flow and meet site objectives.
  • Interface with applicable site support groups on capital and non-capital projects affecting the assigned area, and ensure Good Manufacturing Practice compliance during project planning, execution, and closeout.
  • Collaborate with assigned-area members to facilitate process improvements and risk assessments, and benchmark internal and external Quality Assurance practices to identify efficient and effective practices.
  • Stay informed about evolving regulatory compliance practices and recommend implementation strategies to site leaders.
  • Collaborate in data analysis and create reports on quality metrics and key performance indicators.
  • Initially specialize in one or more responsibilities as needed while developing knowledge of the supported process and applicable current Good Manufacturing Practices.

Desired Qualifications

  • A bachelor's degree; a master's degree in science is desirable.
  • Previous experience in a Lean, process-centric organization with an emphasis on continuous improvement.
  • Multi-site or multi-functional experience.

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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