Senior GMP Auditor – International Life Sciences

Rephine; Barcelona; Presencial; MXN 600.000 - 900.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary

Remote working model

Training and professional development

Descripción de la vacante

Rephine is seeking a GMP Senior Auditor based in Mexico to conduct on-site and remote audits across Mexico, the United States, and Canada. You will ensure compliance with GMP, GDP, GLP, and GCP across pharmaceutical facilities, and review quality systems and documentation.

The role requires travel, strong analytical skills, and fluent English. We offer a remote working model and opportunities in a growing global team with continuous professional development.

Formación

• Proven experience as a GMP Auditor in pharma or healthcare.
• Strong knowledge of GMP and GDP; GLP and GCP a plus.
• Excellent analytical and communication abilities.
• Willingness to travel internationally and work remotely as needed.
• Fluent English; other languages a plus.

Responsabilidades

• Conduct on-site and remote audits of API manufacturers and excipient suppliers.
• Evaluate compliance with GxP regulations and identify gaps and risks.
• Review quality systems and propose corrective actions.
• Stay up to date with regulatory requirements and industry practices.
• Prepare clear, professional audit reports.

Conocimientos

GMP knowledge

GMP Auditor

GDP knowledge

GLP knowledge

GCP knowledge

Analytical thinking

Attention to detail

Communication

Travel readiness

English fluency

Descripción del empleo

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.

Rephine Barcelona is part of the Rephine Group, with offices in Spain (Barcelona), the UK (Stevenage), and China (Shanghai), supporting clients worldwide.

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 global company?

If so, this opportunity is for you.

The Role

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.

Key Responsibilities

• Conduct on-site and remote audits of API manufacturers, excipient suppliers, and pharmaceutical/healthcare facilities.
• Evaluate compliance with GxP regulations and identify gaps, risks, and improvement opportunities.
• Review documentation, procedures, and quality systems, proposing corrective and preventive actions.
• Stay up to date with regulatory requirements and industry best practices.
• Prepare clear, accurate, and professional audit reports.

Requirements

This role is for you if you have:

• Proven experience as a GMP Auditor within the pharmaceutical or healthcare industry.
• Strong knowledge of GMP and GDP (knowledge of GLP and GCP is a plus).
• Excellent analytical and critical-thinking skills.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal abilities.
• Full availability to travel internationally.
• Valid visa or legal authorization to perform audits in the United States and Canada (mandatory).
• Fluent English (additional languages are a plus).

What We Offer

• Competitive salary, aligned with experience and market standards.
• Remote working model, with extensive international exposure.
• A multicultural and highly experienced team always willing to support each other.
• 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.

Why Rephine?

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.

We are looking for professionals who want to grow with us, build a long-term career, and be part of our continued success.

Applications must be submitted in English.