Pharma Validation Specialist: GMP & Compliance

Nouryon

El Pino

On-site

MXN 350,000 - 550,000

Full time

14 days+

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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

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

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