Quality Validation Engineer II

☞ Takeda

View: 150

Update day: 26-11-2025

Location: Lessines Hainaut

Category: Quality Assurance / Quality Control

Industry: Pharmaceuticals

Position: Entry level

Job type: Full-time

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Job content

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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
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    Deadline: 10-01-2026

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