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Senior Design Quality Engineer/ Design Quality Engineer

Healthminds Consulting Verified employer

Actively hiring · Posted today · JEV2611434FEABB33

SalarySalary not disclosed
Experience5–9 yrs
LocationBangalore, Karnataka
Work modeRemote · Full time
Openings1
IndustryMedical / Healthcare

Job description

Job Information

Date Opened

08/10/2026

Job Type

Full time

Industry

Health Care

City

Bengaluru

State/Province

Karnataka

Country

India

Zip/Postal Code

560022

Job Description

Senior Design Quality Engineer/ Design Quality Engineer

Roles & Responsibilities

Ensures that appropriate quality plans are made that include all stages of the life cycle of the product and support Quality Plan design.

Provides effective oversight of the execution of the Quality Plan, any Risk Management activities, and all design-related activities during the product/system lifecycle.

Validates key design inputs like usability, reliability, Performance, supportability, manufacturability, localizability, security, Privacy, serviceability, sustainability, and costs.

Performs assessment of product quality performance and post-market product quality analysis.

Uses post-market analytics and statistics to report on product quality performance in the field (provide feedback to manufacturing, suppliers, or design teams) and initiates field actions when enquired.

Ensure compliance requirements are met during design reviews, design Verification, validation, and design transfer.

Apply and Facilitate design for quality and reliability best practices (FMEA, robust design, V&V, RCA, Problem-solving).

Qualifications

Bachelors Engineering degree with 5-7 years of related experience or Masters degree with 3+ years of related experience -Mechanical/ Electrical/ Electronic or Equivalent Engineering

Engineering Degree or equivalent experience in the medical device industry

3+ years experience with a medical device company preferably

Skill Set

Applied knowledge of appropriate global medical device or consumer product regulations, requirements, and standards (21 CFR Parts 820, ISO13485, ISO14971, MEDDEV, EU MDR, etc.).

Experience or understanding of Software or Hardware development, Verification and Validation, Risk management, RCA, Requirements Management, Design, and Usability.

Understand Sample Size Determination and Statistical Methods, Safety Risk Management (i.e ISO 14971), and Failure Modes and Effects Analysis (FMEA) / Fault Tree Analysis.

Understand a quality system and its development, documentation, and implementation with respect to domestic and international standards or requirements.

Understand the audit process including types of audits, planning, preparation, execution, reporting results, and follow-up.

Be able to develop and implement quality programs, including tracking, analyzing, reporting, and problem solving. .

Key skills

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