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Mantell Associates Logo Mantell Associates · Manufacturing

Manufacturing Analyst

Argentina, Buenos Aires · Job Posted February 17, 2026
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Job Description

This opportunity offers the chance to join a globally recognized biosimilars CDMO and play a key role in ensuring production excellence and regulatory compliance within a high-performance manufacturing environment.

Job Responsibility

  • Support day-to-day production activities and ensure accurate and timely documentation of Batch Records
  • Review raw manufacturing data and QC results to confirm compliance with approved manufacturing specifications and GMP standards
  • Assist in investigations related to deviations, OOS/OOX events, and non-conformances, ensuring appropriate documentation and follow-up actions
  • Collaborate closely with QA and QC teams to maintain GMP compliance across manufacturing processes
  • Contribute to the preparation and participation in internal and external audits
  • Support continuous improvement initiatives within production operations to enhance efficiency, compliance, and documentation accuracy
  • Ensure manufacturing documentation is complete, traceable, and aligned with internal procedures and regulatory requirements

Requirements

  • Experience within a biopharmaceutical manufacturing or related production environment
  • Strong knowledge of GMP requirements and manufacturing documentation standards
  • Demonstrated ability to review and interpret Batch Records, raw data, and QC results
  • Excellent organizational skills with strong attention to detail
  • Effective communication skills and the ability to collaborate cross-functionally
  • Availability to work on-site in Buenos Aires, 5 days per week
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