Nouryon is a global, specialty chemicals leader. Markets and consumers worldwide rely on our essential solutions to manufacture everyday products, such as personal care, cleaning goods, paints and coatings, agriculture and food, pharmaceuticals, and building products. Furthermore, the dedication of approximately 7,650 employees with a shared commitment to our customers, business growth, safety, sustainability and innovation has resulted in a consistently strong financial performance.

We operate in over 80 countries around the world with a portfolio of industry-leading brands.

Validation Specialist

At Nouryon, our integral 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.

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).

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 #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.

Nouryon is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected under applicable federal, state, or local law.

📌 Validation Specialist (Morelos)
🏢 Nouryon
📍 Morelos