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Validations/Verifications Engineer
Job in
Boston, Suffolk County, Massachusetts, 02108, USA
Listed on 2026-07-03
Listing for:
Katalyst Healthcares & Life Sciences
Full Time
position Listed on 2026-07-03
Job specializations:
-
Engineering
Quality Engineering
Job Description & How to Apply Below
Job Title
Role Description s:
Must Have Technical/Functional Skills
Desirable
Skills:
Skills:
EIS:
Medical Device & Regulations ~EIS:
New Product Development (NPD) Methodology and Management
Experience
Required:
4-6 years
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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