Validation Specialist

Nouryon; Los Reyes Acaquilpan; Presencial; MXN 300.000 - 540.000; Jornada completa

Descripción de la vacante

Nouryon is seeking a Validation Specialist in Los Reyes, MX. You will ensure that pharmaceutical processes, equipment, and computerized systems are properly qualified and validated to GMP standards.

The role focuses on IQ/OQ/PQ execution, risk assessment and regulatory audit support, with reporting to the GMP Quality Specialist. The candidate should have 3+ years in pharmaceutical validation, a relevant bachelor’s degree, and English proficiency.

Formación

• Bachelor's degree in Chemical Engineering, Pharmaceutical Chemistry, or Parasitological Chemistry.
• 3+ years of pharmaceutical validation experience and GMP knowledge.

Responsabilidades

• Develop and execute IQ/OQ/PQ protocols.
• Coordinate validation of processes, cleaning and computerized systems.
• 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 lifecycle management of quality documentation.

Conocimientos

English proficiency

Educación

Bachelor's degree in Chemical Engineering, Pharmaceutical Chemistry, or Parasitological Chemistry

Descripción del empleo

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.

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.

In your future role as Validation Specialist you will

• 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.

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.