Validation Specialist

Nouryon; El Pino; On-site; MXN 350,000 - 550,000; Full time

Job summary

Nouryon is seeking a Validation Specialist to join our Los Reyes, MX team. You will ensure that manufacturing processes, equipment, and systems are properly qualified and validated in line with GMP and regulatory requirements.

Reporting to the GMP Quality Specialist, you will develop IQ/OQ/PQ protocols, coordinate validation activities, manage revalidations, and support audits. A chemical engineering or pharmaceutical chemistry degree with at least 3 years of pharma validation experience is

Qualifications

• Bachelor's degree in Chemical Engineering, Pharmaceutical Chemistry, or Parasitological Chemistry.
• Minimum 3 years of experience in pharmaceutical validation (processes and systems) and GMP.
• Language English required (identified as a significant limitation in the local market).

Responsibilities

• Develop and execute IQ/OQ/PQ protocols.
• Coordinate process, cleaning, and computerized systems validation.
• Manage revalidations and maintain the validated state.
• Participate in risk assessments, change controls, and deviation investigations.
• Support internal, corporate, and regulatory audits.
• Prepare and issue final validation and qualification reports.
• Support the preparation and lifecycle management of quality documentation.

Skills

GMP experience

IQ/OQ/PQ knowledge

English proficiency

Education

Bachelor's degree in Chemical Engineering or Pharmaceutical Chemistry

Tools

IQ/OQ/PQ protocols

Job description

Validation Specialist At Nouryon

our global team of Changemakers takes positive action every day, to reach higher collectively and individually. We create innovative and sustainable solutions for our customers to answer society's needs - today and in the future.

We are looking for team members who bring ideas forward, champion others and work together to do better. Does that sound like you?

About the job

Ensure that the processes, equipment, computerized systems, facilities, and critical utilities used in the manufacturing, testing, storage, and distribution of pharmaceutical products are properly qualified and validated, ensuring compliance with GMP and regulatory requirements.

Responsibilities

• Develop and execute IQ/OQ/PQ protocols.
• Coordinate process, cleaning, and computerized systems validation.
• Manage revalidations and maintain the validated state.
• Participate in risk assessments, change controls, and deviation investigations.
• Support internal, corporate, and regulatory audits.
• Prepare and issue final validation and qualification reports.
• Support the preparation and lifecycle management of quality documentation.

We believe you bring

• Bachelor's degree in Chemical Engineering, Pharmaceutical Chemistry, or Parasitological Chemistry.
• Minimum 3 years of experience in pharmaceutical validation (processes and systems) and GMP.
• Language English required (identified as a significant limitation in the local market).

This is a permanent position on a full-time basis, reporting to the GMP Quality Specialist and based in Los Reyes, MX.

Have we got your interest?

For more information about our hiring process, visit: nouryon.com/careers/how-we-hire/

#WeAreNouryon #Changemakers

We have already chosen our sourcing channels for this recruitment and kindly ask not to be contacted by any advertising agents, recruitment agencies or staffing companies.

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