Sr. Design Assurance Engineer

Overview

On Site
USD 125,000.00 - 150,000.00 per year
Full Time

Skills

Mergers and Acquisitions
Product Requirements
Product Design
Product Development
Risk Analysis
Process Modeling
Verification And Validation
IQ
OQ
PQ
Collaboration
Customer Engagement
Design Controls
Risk Management
ISO 13485
ISO 9000
Medical Devices
Regulatory Compliance
EMC
EMI
Technical Drafting
Documentation
FMEA
Testing
Design Of Experiments
Analysis Of Variance
Minitab
Lasers
Privacy
Marketing

Job Details

Location: Marlborough, MA
Salary: $125,000.00 USD Annually - $150,000.00 USD Annually
Description:
The Judge Group is seeking a Senior Design Assurance Engineer for a full time opportunity with a Medical Device Manufacturer. This role will be fully onsite in Marlborough, MA

Title: Senior Design Assurance Engineer

Type: Full Time

Location: Marlborough, MA - Fully Onsite

Candidates should be strong with the following related to disposables or capital medical equipment:

  • Design Controls
  • Product Requirements
  • Testing
  • Risk management
  • Design Validation
  • Internal Design controls
  • Strong Documentation




Responsibilities:
  • Conduct product design control activities for both new and sustaining product development initiatives.
  • Support risk analysis activities, including design and process Failure Modes and Effects Analysis (FMEA).
  • Assist with Process/Design Validation/Verification tasks, encompassing software validation and Installation Qualification/Operational Qualification/Performance Qualification (IQ/OQ/PQ) activities.
  • Collaborate with Design Engineering to create and maintain Design History and Technical Files.
  • Coordinate with third-party testing facilities for compliance testing of IPG products.
  • Aid the regulatory department with FDA, CE, and other regulatory submissions.
  • Execute all other essential duties as assigned.



Requirements:
  • Bachelor's Degree in a scientific or engineering field.
  • Minimum of 8 years in an engineering or quality role within the medical device industry.
  • Strong understanding of Design Controls and Risk Management practices, regulations, and standards (e.g., FDA QSR's, ISO 13485, ISO 14971, IEC 60601, 60825, 62366, 62304) is preferred.
  • Experience supporting medical device compliance testing (e.g., EMC, EMI, IEC) with external testing facilities, such as TV and Intertek.
  • Proficiency in maintaining technical design documentation (e.g., design specifications, verification/validation protocols, DFMEA/PFMEA).
  • Knowledge of advanced statistical methods (e.g., hypothesis testing, DOE, ANOVA, R&R studies, capability analysis, tolerance interval analysis, power and sample size determinations), preferably with statistical software tools such as Minitab.
  • Familiarity with lasers and optical technologies is desired, but not essential.

By providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes. Message & data rates apply and message frequency may vary. Consistent with Judge's Privacy Policy, information obtained from your consent will not be shared with third parties for marketing/promotional purposes. Reply STOP to opt out of receiving telephone calls and text messages from Judge and HELP for help.

Contact:

This job and many more are available through The Judge Group. Please apply with us today!
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.

About Judge Group, Inc.