Job Description

Overview

You are specialized in the design, implementation, and qualification of manufacturing systems, utility infrastructures, and automation technologies. Your work ensures that engineering solutions consistently meet high standards for quality, safety, and productivity, while fully complying with global regulatory frameworks such as cGMP and FDA guidelines. 

Key Responsibilities

Body of Knowledge & Standards

  • Develop and maintain CQV standards, SOPs, and technical guidelines.
  • Provide expert feedback on project compliance and mentor engineers on best practices.
  • Support readiness for regulatory inspections and internal audits.

    • Engineering Projects

  • Lead CQV scope across project phases: design, commissioning, qualification.
  • Define and execute CQV plans, manage resources, and mitigate risks.
  • Coordinate cross-functional teams and ensure seamless project delivery.

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    Job Details

    Location
    Lisbon, Lisbon, Portugal
    Job Type
    Full-time
    Category
    Engineers
    Posted Date
    February 19, 2026
    Deadline
    March 31, 2026