Gmp Senior Auditor (Pharma)

Rephine; A distancia; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A leading company in Life Sciences is seeking a GMP Senior Auditor based in Mexico. This full-time role involves conducting compliance audits across the pharmaceutical sector, including international travel. Ideal candidates will have proven GMP auditing experience, strong analytical skills, and excellent communication abilities. The company offers a competitive salary, remote working options, and a supportive multicultural team environment. Join us for a long-term career in a growing global firm.

Servicios

Competitive salary

Remote working model

Continuous training

Professional development

Team-building activities

Formación

• Proven experience as a GMP Auditor in the pharmaceutical or healthcare industry.
• Fluent in English; other languages are a plus.
• Valid visa/authorization to conduct audits in the US and Canada.

Responsabilidades

• Conduct audits of API manufacturers and healthcare facilities.
• Evaluate compliance with GxP regulations.
• Prepare clear and accurate audit reports.
• Stay updated with regulatory requirements.

Conocimientos

GMP knowledge

GDP knowledge

Analytical skills

Attention to detail

Excellent communication

Critical-thinking skills

Descripción del empleo

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.

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

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.

Seniority Level :

Mid-Senior

Industry :

Pharmaceutical Manufacturing

Employment Type :

Full-time

Job Function :

Quality Assurance

Our recruitment process :

1. Interview with HR
2. Interview with Hiring Manager
3. Last interview
4. Offer