About Rephine Our clients refer to us as the Gold Standard in Life Sciences product quality . We are global experts in Quality Assurance and GxP compliance across Pharmaceutical, Biotech, and Medical Device manufacturing supply chains. Are you passionate about Pharma & Life Sciences? Do you enjoy working in a team, conducting audits, and traveling internationally? Are you ready to contribute to a fast-growing general company? We are looking for a GMP Senior Auditor based in Mexico , with the ability to conduct audits in Mexico, the United States, and Canada . You will join our technical team on a full-time basis and play a key role in ensuring compliance with GMP, GDP, GLP, and GCP standards across pharmaceutical and healthcare facilities. Conduct on-site and remote audits of API manufacturers, excipient suppliers, and pharmaceutical/healthcare facilities . Review documentation, procedures, and quality systems, proposing corrective and preventive actions. Prepare clear, accurate, and professional audit reports.
Proven experience as a GMP Auditor within the pharmaceutical or healthcare industry. Valid visa or legal authorization to perform audits in the United States and Canada (mandatory). Fluent English (additional languages are a plus). Remote working model , with extensive international exposure. Continuous training and professional development programs. A strong company culture with team-building activities, social events, and Rephiesta. Long-term career development in a growing global company . For over 20 years , Rephine has worked closely with some of the largest Life Sciences companies worldwide, supporting them directly at their facilities and helping improve manufacturing quality and compliance. Applications must be submitted in English. Seniority Level: Mid-Senior Pharmaceutical Manufacturing Employment Type: Full-time Job Function: Quality Assurance