Validation Specialist

Nouryon; Los Reyes; Presencial; MXN 420.000 - 540.000; Jornada completa

Descripción de la vacante

Nouryon is seeking a Validation Specialist for its Los Reyes site in Mexico. The role focuses on qualifying manufacturing, testing, storage, and distribution processes and ensuring GMP compliance.

You will develop and execute IQ/OQ/PQ protocols, coordinate validation of processes and systems, and support audits and documentation lifecycle. The ideal candidate has a bachelor’s degree in Chemical Engineering, Pharmaceutical Chemistry, or Parasitological Chemistry and at least 3 years of

Formación

• Bachelor’s degree in Chemical Engineering, Pharmaceutical Chemistry, or Parasitological Chemistry.
• Minimum 3 years of experience in pharmaceutical validation (processes and systems) and GMP.
• English language required.

Responsabilidades

• 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 lifecycle management of quality documentation.

Conocimientos

IQ/OQ/PQ protocols

GMP knowledge

Regulatory compliance

English language

Validation coordination

Educación

Chemical Engineering degree

Pharmaceutical Chemistry degree

Parasitological Chemistry degree

Descripción del empleo

Los Reyes La Paz, México (Bundesstaat), Mexico Apply until: Open until further noticeValidation SpecialistAt 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 jobEnsure 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 willDevelop 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 bringBachelor’s degree in Chemical Engineering, Pharmaceutical Chemistry, or Parasitological Chemistry.Minimum 3 years of experience in pharmaceutical validation (processes and systems) and GMP.LanguageEnglish required (identified as a significant limitation in the local market).Have we got your interest?This is a permanent position on a full-time basis, reporting to the GMP Quality Specialist and based in Los Reyes, MX.Please apply via our online recruitment system. We will not accept applications via e-mail. Once it's with us we will review to see if we have a match between your skills and the role! For more information about our hiring process, visit: nouryon.com/careers/how-we-hire/We look forward to receiving your application!We kindly ask our internal candidates to apply with your Nouryon email via Success Factors.#WeAreNouryon #ChangemakersWe 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.#LI-OnsiteStandardVacancy dataClosing dateOpen until further noticeVacancy numberN0014481OrganizationContinentNorth AmericaCountryMexicoState/Region/ProvinceMéxico (Bundesstaat)SiteLos Reyes La PazBusinessIntegrated Supply ChainJob characteristicsJob areaHealth Safety & QualityHierarchy levelProfessional/Experienced/SpecialistFull time/part timeFulltimeContract typePermanent