This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
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