Validation Process Expert - Manufacturing Science & Tech

Novartis AG; Baarle-Nassau; Híbrido; EUR 46 000 - 85 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Hybrid working options

14 weeks paid parental leave

Insurance plans

Retirement plans

Resumo da oferta

Novartis AG is seeking a Process Expert in Baarle Nassau, Netherlands, to drive validation activities across manufacturing processes. The role focuses on maintaining robust, inspection-ready validation programs throughout the product lifecycle, including master plans and change controls.

The candidate will collaborate across functions to execute validation lifecycle activities, review documentation, and support risk assessments, while ensuring timely completion and compliance with GMP standards.

Qualificações

• Bachelor’s degree in a scientific discipline (Pharmacy/Pharmaceutical Technology/Chemistry).
• 1–2 years experience in Validation or Manufacturing in pharma (GMP).
• Experience in process validation activities within a regulated environment.

Responsabilidades

• Develop and maintain validation master plans for manufacturing, cleaning, packaging, and ongoing verification activities.
• Execute process validation lifecycle activities and support ongoing process verification to maintain process control.
• Review Master Batch Records and change controls for revalidation needs.

Conhecimentos

Pharma manufacturing

English fluent

Dutch advantageous

Project coordination

Problem solving

Formação académica

Bachelor's degree in Pharmacy/Pharmaceutical Technology/Chemistry

Ferramentas

Validation software

Descrição da oferta de emprego

Novartis AG is seeking a Process Expert in Baarle Nassau, Netherlands, to drive validation activities across manufacturing processes. The role focuses on maintaining robust, inspection-ready validation programs throughout the product lifecycle, including master plans and change controls.

The candidate will collaborate across functions to execute validation lifecycle activities, review documentation, and support risk assessments, while ensuring timely completion and compliance with GMP standards.