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Quality Engineer II


Medtronic


Location

Secunderabad | India


Job description

Careers that Change Lives

About Medtronic

We're a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide. Come strengthen your specialized skills and enhance your expertise. We'll support you with the training, mentorship, guidance, and networks you need to advance, and empower you to work in the way that's best for you.

Together, we can confront the challenges that will change the face of healthcare. Join us for a career that change lives. Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together.

In this exciting role asSupplier Quality Engineer-II in Neuroscience portfolio, you will have primary focus responsibility on New Product Introduction and Legacy product. You will interact daily with cross functional team members to ensure business objectives are carefully adhered to. A comprehensive list of the day in the Life is listed below:

The Neuroscience portfolio develops therapies and healthcare solutions that span the care continuum; integrating technologies and applying clinical and economic evidence to increase patient access, improve efficiency of procedures and deliver successful patient outcomes.

As a Supplier Quality Engineer-II you will be a key member of the Medtronic Quality Engineering team and responsible for coordinating suppliers and verifying quality standards in accordance with the company requirements .

A Day in the Life

As the supplier quality engineer II, you will:

  • Ensure that suppliers deliver quality parts, materials, and services.
  • Support and manage Supplier Corrective and Preventive Action plans and projects to improve quality performance of a supplier.
  • Hanlde SCR's ( Supplier change request )
  • Deliver & complete PPAP deliverables for new product & legacy product changes using process validation approach
  • Evaluate supplier performance on periodic basis & take necessary action for continous improvement.
  • May have responsibilities that include Pre-Market Supplier Quality and duties may include: Providing Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products.
  • Colloborate with cross function team for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and ensure product quality and continuous improvement.
  • Ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements.
  • Collaborates with component engineers to develop and deliver the product acceptance sampling strategy, approved supplier list coordination, supplier owned quality deployment, PFMEA,MSA, ,Control Plans andrelevant quality tools and methodologiesfor new products and legacy product.
  • Prepare receiving inspection requirements as required and associated test method validation for all internal Medtronic Test Methods.
  • Support in supplier audit execution and ASL management

Must Have: Minimum Requirements

  • Bachelors degree in Engineering, Science, or Technical Discipline required and 4+ years of quality systems experience. Experience in supplier management is added advantage
  • Good communication skills, both oral and written
  • Previous experience working with global team
  • Comfortable working with international and multi-cultural department and groups in different time zones .

Accurate and delivers quality work, with a sense of urgency

Nice to Have

  • Good interpersonal skills
  • Exposure toFDA Quality System Regulation & ISO 13485 standard
  • Ability to work well under pressure and maintain positive, enthusiastic attitude
  • Eagerness to learn and expand responsibilities
  • Quality certification – CQE,CQA
  • Working knowledge of Standard, Guidance, and Regulations

Lean Six Sigma Yellow belt /Green Belt

  • Ability to work in a fast-paced environment

About Medtronic

Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.

Physical Job Requirements

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)


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