Quality Assurance Engineer 2 at Smith Nephew

pune, maharashtra, India -

Full Time

Start Date

Immediate

Expiry Date

07 Jul, 26

Salary

0.0

Posted On

08 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Design quality engineering, Medical device regulation, Risk management, Design control, Verification and validation, Software quality assurance, FDA 510k, CE Mark, ISO 13485, ISO 14971, IEC 62304, IEC 60601, C programming, Python, Jira, Jama

Industry

Medical Equipment Manufacturing

Description

Quality Assurance Engineer 2 Location: Kharadi, Pune Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living. At Smith+Nephew, we’re looking for a Senior Manager, Data Services – Data Architecture to join our diverse and collaborative Data & Analytics team. In this role, you’ll lead the design and delivery of modern, scalable, and inclusive data architecture that powers our enterprise cloud data platform and enables a wide range of data, analytics, quality, and research solutions. You’ll partner closely with business and technology teams to transform our on-premise data environment, build robust data engineering and transformation frameworks, and deliver high-quality, efficient, and reliable data products using Snowflake on AWS and emerging technologies. You’ll also guide solution architects, promote agile and inclusive ways of working, and champion best practices that empower teams across the organization to drive data-driven insights and innovation. What will you be doing? Role Overview - 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 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. Responsibilities: (50%) - Provide quality leadership to new product development (NPD) and/or sustaining project teams as the Quality Engineering representative on projects requiring FDA 510k, CE Mark, and international regulatory approval. Work with a team 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 towards product development milestones and submission filings, including design reviews, risk management, requirements and verification traceability. (30%) - Ensure compliance to product specific standards, cGMP, QSR, US FDA, ISO, IEC, UL, EN, MDD / MDR, and NMPA requirements. Ensure that all the responsibilities within the scope of this job comply with the scope of the Quality System. (20%) – Provide Quality Management System support for the local site(s) as needed. What will you need to be successful? Education - Include any educational needs applicable to the job. B. S. in Electrical, Computer, or Biomedical Engineering or related discipline, M.S. in Engineering preferred Licenses/ Certifications/ Competencies/ Experience License/certification: ASQ CQE / CRE (preferred, not required) 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) Team player MS Office and MS Excel software proficiency Equipment proficiency preferred with Oscilloscopes, Function Generators, and Digital Multimeters Software proficiency preferred in the following: Requirement management tool (such as Jama or Cockpit) Defect tracking tool (such as Jira) C / Python programming languages Experience: 2+ years in medical device or related industry with B.S. degree OR 1+ years in medical device or related industry with M.S. degree You Unlimited. We believe in crafting the greatest good for society. Our strongest investments are in our people and the patients we serve. Inclusion + Belonging: - Committed to Welcoming, Celebrating, and Thriving. Learn more about our Employee Inclusion Groups on our website (https://www.smith-nephew.com/). Other reasons why you will love it here! Your Future: Major medical coverage + policy exclusions and insurance non-medical limit. Educational Assistance. Work/Life Balance: Flexible Personal/Vacation Time Off, Privilege Leave, Floater Leave. Your Wellbeing: Parents’/Parents-in-Law’s Insurance (Employer Contribution of 8,000/- annually), Employee Assistance Program, Parental Leave. Flexibility: Hybrid Work Model (For most professional roles) Training: Hands-On, Team-Customized, Mentorship Extra Perks: Free Cab Transport Facility for all employees; One-Time Meal provided to all employees as per shift. Night shift allowances. Stay connected by joining our Talent Community. We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day. Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N. Explore our website and learn more about our mission, our team, and the opportunities we offer. Smith+Nephew is a global medical technology company. We design and manufacture technology that takes the limits off living. We support healthcare professionals to return their patients to health and mobility, helping them to perform at their fullest potential. From our first employee and founder, T.J. Smith, to our team today, it’s our people who make Smith+Nephew a unique place. Yes, we love to innovate and develop exciting technologies, and we offer competitive salaries and progressive benefits. But it’s our culture - of Care, Collaboration and Courage - that really sets us apart. Through a spirit of ownership and can-do attitude we work together to win. We’re a company of people who care about each other, about our customers and their patients, and about our communities. Together, we fulfill our shared purpose of Life Unlimited.

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Responsibilities

The Design Quality Engineer will lead quality activities for new product development, ensuring compliance with regulatory standards such as FDA 510k and CE Mark. They will manage design controls, risk management documentation, and verification/validation processes for medical devices containing software.