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CSL

Develops and delivers biotherapies and vaccines

Manager, CMO Quality

Regulatory & Quality (Life Sciences)Updated on Nov 15
Full-timeArgentinaNo salary listed

About the Job

Requirements

  • A bachelor's degree or higher in Pharmacy, Chemistry, Biology, Biochemistry, or a related scientific discipline.
  • A minimum of 5 years of experience in a GxP environment within the pharmaceutical, biotech, or another regulated industry.
  • Demonstrated knowledge of FDA, PIC/S, EU GMP, TGA, and Health Canada regulatory frameworks.
  • Ability to work effectively in a global matrix organization.
  • Strong quality system knowledge across internal and external manufacturing environments.
  • Fluency in written and spoken English and Spanish.

Responsibilities

  • Serve as the primary regional quality interface for assigned Contract Manufacturing Organizations (CMOs) and foster strong partnerships.
  • Ensure CMO quality systems align with CSL Seqirus standards and applicable regulatory requirements.
  • Represent CSL Seqirus Quality in Joint Operational Meetings, Business Reviews, and on-site CMO visits.
  • Draft, negotiate, and maintain CMO Quality Agreements in compliance with FDA, EMA, PIC/S, TGA, and Health Canada regulations.
  • Oversee execution of Quality Agreement commitments, including training, recalls, and complaint management.
  • Review, assess, challenge, and approve CMO deviations and corrective and preventive actions (CAPAs) to ensure product quality and compliance.
  • Manage CMO-initiated changes and communicate relevant updates to marketing authorization holder (MAH) stakeholders.
  • Review and approve good manufacturing practice (GMP)-controlled documents, including standard operating procedures (SOPs), specifications, and validation reports.
  • Track and report CMO quality performance through globally aligned key performance indicators (KPIs).
  • Identify quality trends and ensure timely corrective actions are implemented.
  • Escalate critical quality issues to senior stakeholders and drive resolution.
  • Harmonize quality processes across the CMO network, including change management, batch record review, complaints, and recalls.
  • Enhance CMO Quality Maturity and execute Quality Road Maps.
  • Support regulatory inspections and audits at CMO sites as needed.
  • Assess and communicate potential regulatory impacts on CSL Seqirus business.
  • Support technology transfer, product launches, and regulatory submissions for new CMO projects.
  • Act as the Quality subject matter expert (SME) in cross-functional commercial readiness teams.

Desired Qualifications

  • Prior experience in CMO or third-party quality management is highly preferred.

About the Company

CSL

Develops and delivers biotherapies and vaccines

CSL is a global biotechnology company that develops and delivers biotherapies and influenza vaccines. It focuses on plasma-derived and recombinant therapies for rare and serious diseases and sells to healthcare providers, hospitals, and governments across the Americas, Asia Pacific, and Europe. Its product range includes treatments for rare diseases, influenza vaccines, and antivenoms, produced through its R&D, manufacturing, and distribution operations. CSL differentiates itself by offering the broadest portfolio of plasma-derived and recombinant therapies and by leveraging its global footprint and emphasis on diversity to reach diverse markets. The company’s main goal is to save lives and protect health by expanding access to high-quality therapies and vaccines worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Parkville, Australia
Founded
1916

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