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Validations/ Verifications Engineer

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Onsite

Validations/ Verifications Engineer

Katalyst CRO

Validations/ Verifications Engineer

Skills

Risk Management

1 month ago

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Important information


Contract type:

Freelance / Contract

Location:

Boston, MA, USA

Work mode:

Onsite

Published on:

14 September 2026

What they need


Role Descriptions Must Have Technical/Functional Skills

Desirable Skills Skills: EIS: Medical Device & Regulations ~EIS: New Product Development (NPD) Methodology and Management Experience Required: 4-6 5+ years of work experience in medical device industry Required

  • A bachelor's degree in Technical or Scientific discipline
  • 5+ years of work experience in medical device industry
  • Experience conducting Process Verifications / Validations
  • Experience conducting Design and/or Process Failure Modes Effects and Analysis
  • Excellent problem solving and decision-making skills
  • Interpersonal skills that foster collaboration as they relate to technical situations
  • Strong initiative and follow-through in executing project responsibilities, overcoming obstacles, and balancing multiple priorities effectively through strong technical and/or project leadership experience
  • Design Quality Engineering experience
  • Design Control experience

Preferred

  • An advanced degree
  • A bachelor's degree in mechanical engineering or Bioengineering
  • New Product Development experience
  • Experience with Blueprint reading/literacy/inspection methods & techniques including GD&T
  • Strong experience with Design Excellence, Six Sigma, or Lean
  • Spanish as a second language

Roles & Responsibilities

  • Conducting Process Verifications / Validations
  • Design and/or Process Failure Modes Effects and Analysis
  • Blueprint reading/literacy/inspection methods & techniques including GD&T
  • People Management: ability to ensure small delays don’t derail critical items and work with embedded team on site to ensure smooth implementation.
  • Strategic Mindset: ability to think bigger picture and work with Senior leadership on long term strategy for area/site.
  • Performing risk management, execute product testing
  • Work on Quality System, including, but not limited to corrective & preventive actions, nonconforming materials, risk management, and medical device regulations

Generic Managerial Skills, If Any

  • Required to have good communication skills both written & verbal and be computer literate (Word, Excel, outlook Email - a must).
  • Strong interpersonal, organizational, written and oral communication skills
  • Dependable, somewhat assertive, reasonably organized, resourceful and communicative with an ability to adapt and learn quickly as well as follow verbal and written instruction, detail oriented.

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