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Validation Engineer Boxmeer SIRE Life Sciences

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Gevraagd

  • 37 - 40 uur
  • HBO of hoger
  • Medior/Senior

Aanbod

  • Vast contract
 

Vacature in het kort

Boxmeer
Join a global leader in animal health as a Validation Engineer, where you'll play a pivotal role in advancing the Science of Healthier Animals. You'll be at the forefront of Equipment and Sterilization Validation, overseeing commissioning and qualification activities for engineering projects. Enjoy working with cutting-edge technologies that support animal identification, traceability, and monitoring. Collaborate with cross-functional teams and contribute to impactful projects in a dynamic environment. Read on to discover how you can shine in this role.
 

Over het bedrijf

SIRE Life Sciences
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The company
As a global leader in animal health, we are dedicated to advancing the Science of Healthier Animals. Our portfolio includes a broad range of veterinary medicines, vaccines, and health management solutions and services. We also offer a comprehensive suite of connected technologies that support animal identification, traceability, and monitoring.

Role Description
As a Validation Engineer, you are responsible for Equipment Validation and Sterilization Validation, planning, coordinating, and overseeing commissioning and qualification activities across engineering projects.

Responsibilities

  • Provide validation support for projects, particularly cleaning and sterilization validation
  • Develop and author Validation Master Plans (VMPs)
  • Create and update SOPs and related documentation
  • Write validation protocols and final reports
  • Execute validation studies and analyze collected data
  • Troubleshoot and resolve technical issues during study execution
  • Collaborate with cross-functional teams and work independently as needed
  • Work under moderate supervision with sound knowledge and skills relevant to the role
Requirements
  • HBO/WO degree in a technical or scientific field
  • Experience in equipment validation and sterilization validation
  • 3–5 years of relevant experience in pharma or food industry (QA or C&Q)
  • Strong coaching, communication, and problem-solving skills
  • Fluent in Dutch and English
  • Experience with GMP, commissioning, qualification, and (optionally) CSV
Other Information
Are you interested in this or a similar role? Click the apply button below, and I will contact you as soon as possible.
 

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