Quality Validation Engineer II

☞ Takeda

Ver: 150

Día de actualización: 26-11-2025

Ubicación: Lessines Hainaut

Categoría: Seguro de Calidad / Control de Calidad

Industria: Pharmaceuticals

Posición: Entry level

Tipo de empleo: Full-time

Loading ...

Contenido de trabajo

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Summary

Job Description

The Quality Validation Engineer II is responsible to perform the quality oversight of validation activities including process, product, cleaning, equipment, material, shipping, IT and computerized systems validation at the Lessines facility.

She/He will have authority to make decisions in her/his projects, and if needed is supported by a Quality Validation Senior Engineer or Quality Validation Lead.

Essential Duties And Responsibilities

  • Review/approve validation documentation from projects (RA, DQ, IQ, OQ, PQ, PPQ) and associated specification documents (URS, Functional/ Design Specification) with a priority to complex projects.
  • Coach of Quality Validation Engineers I, or external contributors review of documents prepared by Quality Validation Engineers I or external contributors
  • Review periodic evaluation maintaining the accurate validation state of processes, facilities and systems ensuring compliance to procedures and regulatory requirements
  • Provide quality guidance for the development strategy and risk analysis related to the validation
  • Provide support in quality-related issues, including GMP regulations, compliance with internal SOPs, and all aspects of safe, reliable and consistent operation of the system with the support of a Quality Validation Senior or the Quality Validation Lead, if needed.

    • Main Skills & Experience
    • Knowledge of regulations related to validation activities in pharmaceutical industry
    • Exposure and/or knowledge of Validation and Engineering functions.
    • Quality pillars experience (QA, QC, Systems and Compliance) including cGMP regulations.
    • Strong oral and written communication skills with teams, peers, global partners
    • Teamwork skills.
    • Ability to develop and maintain good working relationships with customer groups and support a positive environment of teamwork and collaboration.
    • Critical thinking and demonstrated problem solving skills.
    • Good Organizational skills
    • Assertiveness
    • Autonomy
    • Flexibility

    Education
    • Master degree with at least 2 years of experience in Validation and/or Quality Assurance/Systems – pharmaceutical industry, or equivalent.

    Locations

    BEL - Lessines

    Worker Type

    Employee

    Worker Sub-Type

    Regular

    Time Type

    Full time
    Loading ...
    Loading ...

    Plazo: 10-01-2026

    Haga clic para postularse como candidato gratuito

    Aplicar

    Reporte trabajo
    Loading ...

    TRABAJOS SIMILARES

    Loading ...
    Loading ...