Smith+Nephew

medical device

StaffDesignQualityEngineer

Pune, India FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Lead candidates.

The Brief

“Staff Design Quality Engineer at Smith+Nephew. Skills: Design Quality Engineer, Medical devices, Embedded Software. Provide quality leadership to new product development. Support Smith and Nephew QMS”

What You'll Achieve.

Ensure that the finished devices will be safe and effective; Ensure that the finished devices conform to applicable regulatory requirements

Industry & Context.

medical device
Problems you'll solve

Provide and implement solutions to quality problems

What They're Looking For.

Must Have

B. S. in Electrical, Computer, or Biomedical Engineering or related discipline, 8+ years in medical device or related industry with a B. S. degree OR 6+ years in medical device or related industry with a M. S. degree, Understanding the impact of regulatory requirements (eg. GMP’s, ISO 13485, ISO 14971, IEC 62304, IEC 60601, MDD / MDR, and NMPA) on Smith + Nephew’s products, Need to be able to make sound decisions with attention to details, Must be able to provide and implement solutions to quality problems, Ability to plan and schedule multiple projects and tasks, Excellent oral / written communication skills (GDP knowledge critical), MS Office and MS Excel software proficiency

Nice to Have

M. S. in Engineering, ASQ CQE / CRE, Equipment proficiency preferred with Oscilloscopes, Function Generators, and Digital Multimeters, Software proficiency preferred in the following: Requirement management tool (such as Jama or Cockpit), Software proficiency preferred in the following: Defect tracking tool (such as Jira), Software proficiency preferred in the following: C / Python programming languages

What You'll Do.

Provide quality leadership to new product development

Support Smith and Nephew QMS

Support new product development activities

and evaluation criteria

Support completion of Design Control

Support Risk Management requirements

Ensure finished devices are safe and effective

Ensure conformity to regulatory requirements

Lead efforts to develop verification and validation test methods

Generate/approve/manage software and design verifications

Generate/approve/manage design validations

Generate/approve/manage usability / human factors

Generate/approve/manage reliability testing

Generate/approve/manage process validations

Generate/approve/manage supplier qualifications

Generate/approve/manage test methods

Generate/approve/manage capability studies

Generate/approve/manage risk management documentation

Interface with R&D and manufacturing engineers

Identify and resolve defects

Identify and resolve product quality issues

Lead project cross-functional communication

Ensure compliance to product specific standards

Ensure compliance to cGMP

Ensure compliance to QSR

Ensure compliance to US FDA

Ensure compliance to ISO

Ensure compliance to IEC

Ensure compliance to UL

Ensure compliance to EN

Ensure compliance to MDD / MDR

Ensure compliance to NMPA

Ensure responsibilities comply with Quality System

Provide Quality Management System support

How You'll Work.

Team & Collaboration

Quality Engineering representative on projects; Interface with R&D and manufacturing engineers; Lead project cross-functional communication

Communication Scope

Excellent oral / written communication skills; GDP knowledge critical; Cross-functional communication

Process & Methodology

Ability to plan and schedule multiple projects and tasks, Product development milestones

Full Job Description

## **Role: Staff Design Quality Engineer** ## **Location: Kharadi, Pune** ## ## **Life Unlimited.** At Smith+Nephew, we design and manufacture technology that takes the limits off living. At Smith+Nephew, as Staff Design Quality Engineer would be reporting into the Quality Department, this role has responsibility for supporting Smith and Nephew QMS and new product development activities for Arthroscopic Enabling Technologies and ENT products as a lead Design Quality Engineer. Technological areas of focus for this position include determining methods, techniques, and evaluation criteria for medical devices containing embedded Software, specifically High Frequency surgical equipment. The Design Quality Engineer will support the completion of Design Control and Risk Management requirements and help to ensure that the finished devices will be safe and effective and conform to applicable regulatory requirements. **What will you be doing?** * **(50%) -** Provide quality leadership to new product development project (PDP) and/or sustaining project teams as the Quality Engineering representative on projects requiring FDA 510k, CE Mark, and international regulatory approval. Lead efforts to develop verification and validation test methods and procedures to ensure that the appropriate tests are conducted to assure that embedded software, analog and digital electronic circuits, and support hardware used within instrument products meet the required specifications/standards and that the safety and reliability of products are established. Generate/approve/manage software and design verifications, design validations, usability / human factors, reliability testing, process validations, supplier qualifications, test methods, capability studies, and risk management documentation to support the product DHF. Interface with R&D and manufacturing engineers to identify and resolve defects and product quality issues. Lead project cross-functional communication of status and deliverables to

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