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Katalyst Healthcares & Life Sciences

Validations/ Verifications Engineer

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What they do

A Verification Engineer is responsible for ensuring that a product meets its specifications and requirements. Designs methods to test products, identify bugs in software products, and communicates with cross-functional teams, ensuring product development procedures and outcomes meets regulations. Primary objective is to verify that the system functions correctly and reliably according to its design and intended purpose.

$129,832 / year median in Massachusetts

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Job Description

Validations/ Verifications Engineer Katalyst Healthcares & Life Sciences - 4.0 Boston, MA Job Details Contract 14 hours ago Qualifications Microsoft Outlook Medical device testing Team leadership Production validation processes Leading team collaboration initiatives Design controls Engineering quality assurance
Full Job Description 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.