TransPerfect is looking for a Quality Assurance Auditor Jr to join our QA team In this role, you will play a key part in maintaining and continuously improving our Integral Quality Management System (QMS), ensuring compliance with international standards, regulatory requirements, and industry best practices. You will work closely with internal teams, clients, suppliers, and external auditors to support audit activities, drive corrective and preventive actions (CAPA), and promote a culture of quality and continuous improvement.

Key Responsibilities
• Plan, coordinate, and conduct internal, external, customer, and supplier audits.
• Support customer audits and regulatory inspections, including preparation, coordination, and follow-up.
• Manage audit findings and ensure timely implementation of corrective and preventive actions (CAPA).
• Monitor compliance with international standards and regulations, including ISO 9001, ISO 17100, and GxP.
• Analyze audit results, identify trends, and prepare reports for management.
• Contribute to the development and continuous improvement of QA processes, policies, and procedures.
• Collaborate with internal and external stakeholders to ensure quality standards and customer requirements are met.

Requirements:




• Bachelor’s degree or equivalent.
• Excellent written and verbal communication skills in English.
• At least 2 years of experience in the Life Sciences industry, preferably in Quality Assurance or audit-related activities.
• Experience with QA audits, CAPA, change control, deviation management, complaint handling, and regulatory compliance.
• Knowledge of international quality standards such as ISO 9001, ISO 17100, ISO 27001, and/or GxP.
• Experience managing multiple projects and audits simultaneously.
• Strong analytical, organizational, problem-solving, and communication skills.
• Proficiency in Microsoft Office. Nice to Have:
• Experience in regulated industries such as Pharmaceutical, Healthcare, CRO, or Medical Devices.
• Lead Auditor Certification (ISO 9001, ISO 27001, etc.).
• Knowledge of clinical development processes, ICH E6, and 21 CFR Part 11.
• Experience with Six Sigma, Lean, or other quality improvement methodologies.
• Fluency in an additional language. ? Interested in applying? Please submit your CV in English. #Hiring #QualityAssurance #QAAuditor #LifeSciences #Auditing #QualityManagement #TransPerfect #Careers #Regulatory Affairs

📌 Quality and Regulatory Affairs Auditor Jr (Argentina)
🏢 Transperfect
📍 Argentina