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Validation Engineer

Job in Boxborough, Middlesex County, Massachusetts, 01719, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-07-22
Job specializations:
  • Engineering
    Quality Engineering, Test Engineer
Job Description & How to Apply Below
Location: Boxborough

Roles & Responsibilities :

  • Test Stand & Lab View experience along with some Manufacturing equipment validations (IQ/OQ /PQ) experience
  • Test Engineer that can help qualify Automated Functional Testers.
  • Would be responsible for writing all the documentation (requirement| trace matrix| protocols| reports using the Healthcare templates) and executing the validations.
  • The code for the testers will be written by an internal resources with whom Candidate would work closely in order to complete the paperwork and qualify the systems.
  • Candidate may also help assemble the hardware side of the tester.
  • Good To have - Background in Test Stand | Lab View that would be a bonus to help debug and trace requirements.
  • Qualify automated functional test systems and support troubleshooting.
  • Develop and maintain validation documentation| including requirements| trace matrices| test protocols| and reports.
  • Execute verification and validation testing| document results| and manage deviations.
  • Ensure compliance with internal quality systems and regulatory standards.
  • Collaborate with cross functional teams to support product testing and continuous improvement.
Requirements:
  • Bachelors degree in Engineering or related discipline.
  • Experience in verification validation testing| preferably in medical devices or other regulated industries.
  • Familiarity with automated test systems and documentation best practices.
  • Strong analytical| documentation| and problem solving skills.
  • About Client Medical device customer USP of the Role and Project
  • Would be responsible for writing all the documentation (requirement| trace matrix| protocols| reports using this.
  • The code for the testers will be written by an internal resources with whom this person would work closely in order to complete the paperwork and qualify the systems.
  • They may also help assemble the hardware side of the tester.
  • Candidate should have experience as tester development for Manufacturing
  • Candidate should have experience with the validations within the MFG environment - IQ| OQ| PQ
  • Responsible for writing all the documentation (requirement| trace matrix| protocols| reports using the Healthcare templates) and executing the validations.
  • If they have background in Test Stand Lab View that would be a bonus to help debug and trace requirements.
  • Essential

    Skills:

    Functional Testing
  • Skills:

    Functional Testing
  • Skills:

    MFG/PRO Domain (QAD)
  • Experience

    Required:

    4-6
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