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Resilience

Biologics and sterile injectables CDMO

Associate 2 - Quality Assurance

Regulatory & Quality (Life Sciences)Posted on Nov 13
Full-timeWest Chester Township, OH, USA

About the Job

Requirements

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

Responsibilities

  • Maintain a high level of understanding of relevant production processes and quality systems.
  • Perform QA review and approval of GMP documentation that directly impacts activities performed by, and facilities utilized in, corresponding areas, including Change Requests; Batch Records and associated documentation; Product and Component Release transactions in SAP; Quality Investigations, including Deviations and Product Complaints; Validation Plans, Protocols and Reports; and Standard Operating Procedures.
  • Collaborate with and influence other Quality professionals across the organization to ensure consistent application and execution of key quality systems.
  • Execute QA processes, including batch record review, product disposition, and quality issue resolution, to maintain the flow of products and documents and meet site objectives.
  • Interface with applicable site support groups on capital and non-capital projects that impact the PET or assigned area, and proactively ensure GMP compliance during planning, execution, and closeout.
  • Collaborate with and influence other PET or assigned-area members to facilitate process improvements and risk assessments; benchmark internal and external QA practices to identify efficient and effective practices.
  • Stay abreast of evolving regulatory compliance practices and recommend implementation strategies to site leaders.
  • Collaborate in data analysis and report creation on quality metrics and key performance indicators.
  • The incumbent may initially specialize in one or more responsibilities while developing knowledge of the supported process and applicable cGMPs.

Desired Qualifications

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

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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