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Smith+Nephew

Global medical devices for orthopedics

Design Quality Engineer 2

Biomedical Engineering & Medical Devices +1Posted on Nov 11
Full-timeAustin, TX, USANo salary listedIn-person

About the Job

Requirements

  • A four-year technical degree is required.
  • Two to five years of experience in the medical device industry is required.
  • Experience with design verification and validation, process or sterilization validation, risk management, test methods, supplier qualification, and investigation or corrective and preventive action (CAPA) activities is required.
  • Working knowledge of relevant medical device regulations and standards, including U.S. Food and Drug Administration (FDA), Quality System Regulation (QSR), current Good Manufacturing Practice (cGMP), International Organization for Standardization (ISO), and European Union Medical Device Regulation (EU MDR) requirements is required.

Responsibilities

  • Provide quality leadership for new product development project teams as the Quality Engineering representative, partnering with cross-functional teams.
  • Generate, approve, and manage design verification, design validation, sterilization validation, process validation, supplier qualification, and test method activities.
  • Develop protocols, capability studies, and risk assessments to support product safety, reliability, and overall risk management.
  • Ensure compliance with applicable product standards and regulatory requirements, including cGMP, QSR, U.S. FDA, ISO, International Electrotechnical Commission (IEC), Underwriters Laboratories (UL), European Norm (EN), and EU MDR requirements.
  • Support manufacturing operations with expertise in product requirements, inspection and test methods, root cause investigations, and issue resolution.
  • Partner with external laboratories and suppliers to communicate product and process requirements and assess capabilities.
  • Support continuous improvement and compliance activities, including CAPA resolution and nonconformance investigations.
  • Support Post Market Surveillance, Quality Management Reviews, and internal and external audits or inspections.

Desired Qualifications

  • A bachelor's degree in biomedical or mechanical engineering is highly preferred.
  • Familiarity with process development and new product development is a plus.

About the Company

Smith+Nephew

Global medical devices for orthopedics

Smith+Nephew is a global medical technology company that designs and makes medical devices for orthopaedics, sports medicine, and advanced wound care. Its products help surgeons treat joints and soft tissues and support patient recovery, including knee repair systems, single-use negative pressure wound therapy devices, and other extremity orthopaedic products. These devices are used in hospitals and clinics to perform procedures and support healing, often after surgery or injury. The company differentiates itself with a broad, worldwide product portfolio and collaborations with healthcare organizations to improve care and efficiency for patients and providers. Its goal is to improve patient outcomes, streamline medical procedures, and expand access to advanced medical solutions around the world.

Company size
10,001+
Company stage
IPO
Headquarters
Watford, United Kingdom
Founded
1856

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