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Validations/ Verifications Engineer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts • 16d ago

Full-time

Validation Engineer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts • 16d ago

Full-time

Senior Validation Engineer I

Takeda pharmaceutical

Lexington, Massachusetts • Today

Full-time

USD 104,541.00 - 141,240.00 per year

Senior Verification Engineer

Analog Devices, Inc.

Wilmington, Massachusetts • Today

Full-time

USD 110,385.00 - 151,808.00 per year

Validation Engineer

Katalyst Healthcares and Lifesciences

Boxborough, Massachusetts • 16d ago

Full-time

Computer Systems Validation Engineer

Praxis Precision Medicines

Remote • Today

Full-time

USD 150,000.00 - 178,000.00 per year

Cybersecurity Validation and Test Engineer

Amyx Inc

Remote • Today

Full-time

USD 100,000.00 - 140,000.00 per year

Engineering Manager, Verification and Validation (STATCOM)

GE Vernova

Remote • Today

Full-time

USD 113,200.00 - 188,800.00 per year

Senior Software Verification & Validation Engineer

Draper

Cambridge, Massachusetts • Today

Full-time

USD 75,000.00 per year

Job Details

Skills

EIS
Management
Conflict Resolution
Problem Solving
Decision-making
Collaboration
Project Management
Quality Assurance
Design Controls
Mechanical Engineering
Product Development
Six Sigma
Lean Methodology
Spanish
Blueprint
Inspection
GD&T
People Management
Embedded Systems
Leadership
Product QA
Risk Management
Medical Devices
Microsoft Excel
Microsoft Outlook
Communication
Dependability
Organized
Training
Attention To Detail

Summary

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.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: 44e9a40cf28c7bb613134b1a91437134
Posted 30+ days ago

Fitment

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Similar Jobs

Validation Engineer

Boston, Massachusetts

•

16d ago

Job Summary: We are seeking an experienced Validation Engineer to support system-level Verification & Validation (V&V) activities for medical device products. The role involves planning and executing V&V activities, developing and executing validation protocols, supporting design verification, and ensuring compliance with FDA, ISO 13485, and internal quality system requirements. Experience with infusion pump systems or similar electromechanical medical devices is preferred. Roles & Responsibilit

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Staff Engineer, Quality

Waltham, Massachusetts

•

Today

Work Flexibility: Onsite Join Stryker's Amplitude Vascular Systems (AVS) team in Waltham, Massachusetts as a Staff Quality Engineer. In this role, you will support manufacturing operations, supplier quality, and process performance across both existing and new products. Working closely with operations, engineering, suppliers, and cross-functional partners, you will help ensure products and manufacturing processes meet quality standards, regulatory requirements, and customer expectations. This

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USD 107,200.00 - 178,600.00 per year

Product Design Quality Engineer

Cambridge, Massachusetts

•

16d ago

Job Description: The Product Design Quality Engineer is responsible for supporting quality throughout the product development lifecycle by ensuring compliance with regulatory requirements, quality standards, and design control processes. This role partners with cross-functional teams to integrate quality into product development, risk management, validation, and manufacturing transfer activities. Responsibilities: Support Design Control activities throughout the product development lifecycle in

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Engineering Manager

Danvers, Massachusetts

•

Today

We anticipate the application window for this opening will close on - 19 Nov 2026 Position Description: Engineering Manager for Medtronic, Inc. in Danvers, MA. Plan, direct and implement various aspects of the design and development of new medical device products. Develop, evaluate, implement and maintain technical quality assurance and control systems standards in extrusion and assembly manufacturing pertaining to materials, techniques, and products. Select, develop and evaluate personnel to e

Full-time

USD 178,000.00 - 213,000.00 per year

Job Details

Skills

EIS
Management
Conflict Resolution
Problem Solving
Decision-making
Collaboration
Project Management
Quality Assurance
Design Controls
Mechanical Engineering
Product Development
Six Sigma
Lean Methodology
Spanish
Blueprint
Inspection
GD&T
People Management
Embedded Systems
Leadership
Product QA
Risk Management
Medical Devices
Microsoft Excel
Microsoft Outlook
Communication
Dependability
Organized
Training
Attention To Detail

Summary

Dice Id: 91116760
Position Id: 44e9a40cf28c7bb613134b1a91437134
Posted 30+ days ago

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Create job alert

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