Product Steward (M / F / D)

buscojobs España; Zaragoza; Presencial; EUR 35.000 - 55.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical industry is seeking a dedicated Product Steward to enhance product quality and processes. This role involves working with the MS&T team, ensuring compliance, and monitoring critical process variables, all while fostering patient-centric improvements. Join a passionate team focused on making a tangible impact in healthcare.

Formación

• BSc. in Pharmacy, Biotechnology, Chemical or Pharmaceutical Technology required.
• Strong knowledge in statistical activities necessary.
• Thorough understanding of manufacturing processes and related equipment required.

Responsabilidades

• Maintain oversight and knowledge of the entire manufacturing process.
• Ensure inspection readiness and support root cause investigations.
• Track and evaluate product performance, detect issues, and implement CAPAs.

Conocimientos

Statistical activities

Manufacturing processes knowledge

Proficiency in Spanish

Proficiency in English

Educación

BSc. in Pharmacy

Ms. Sc. in Pharmaceutical Industry

Herramientas

Minitab

Descripción del empleo

We are seeking a dedicated Product Steward to join our team. In this role, you will be instrumental in enhancing the quality of our products and processes. You will collaborate with a talented team, all committed to significantly improving the lives of our patients. If you are passionate about making a meaningful impact, we would love to hear from you.

This role will work directly with the MS&T team and reports to the MS&T Site Head RLT.

About The Role

Key Responsibilities :

Your Responsibilities Include, But Are Not Limited To

• Maintain oversight and knowledge of the entire manufacturing process performed on site.
• Monitor all critical variables and key variables as appropriate using statistical analysis and conduct regular product-specific data trending.
• Ensure inspection readiness for all process-related aspects of assigned products.
• Track and evaluate product performance, trending, detect issues, and implement CAPAs.
• Support root cause investigations of process failures, initiate and lead product improvement projects, assess technical changes and their feasibility.
• Support registration activities and the creation / maintenance of the Master Batch Record.
• Ensure the continued validation of processes, cleaning, and ongoing verification.
• Establish the ongoing verification report (OPV) on time in alignment with the APQR.
• BSc. in Pharmacy, Biotechnology, Chemical or Pharmaceutical Technology.
• Strong knowledge in statistical activities.
• Thorough understanding of manufacturing processes and related process equipment.
• Proficiency in Spanish & English.
• Knowledge of RLT, OPV, and Minitab.
• Ms. Sc. in Pharmaceutical Industry.

Why Novartis

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other to achieve breakthroughs that change patients’ lives. Create a brighter future together .

Benefits and Rewards

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally.

Commitment To Diversity And Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams that are representative of the patients and communities we serve.

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