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Medtronic Quality Engineer II in Nanakramguda, India

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Responsible for providing quality engineering support in design, development, and

sustaining activities for low complexity and complex medical device products.

• Review new and modified product design documentation for quality

characteristics, including manufacturability, serviceability, testability, reliability, and

product requirements.

Responsibilities may include the following and other duties may be assigned

eview new and modified product design documentation for quality characteristics,

including manufacturability, serviceability, testability, reliability, and product requirements.

• Ensure that product development projects and changes to existing products are

conducted in compliance with FDA Quality System Regulations.

• Participate on cross-functional teams to review marketing requirements and to develop

concise, unambiguous, con-conflicting,, and feasible product requirements that support

the market needs

• Complaint Handling Experience for the medical devices products

• Participate on cross-functional teams to develop product risk management file (risk

management plan, risk assessments, DFMEA, and risk management report).

• Partner with Software Engineering to assess risk, develop software design plans and

documentation, ensure code and integration reviews occur, and to demonstrate software

capability and maturity.

• Strong in software design and development, software verification and validation activities

• Oversee testing and analysis for standards and product requirements compliance.

• Provide guidance and direction for sample size and statistical analysis of verification and

validation test results.

• Ensure successful transfer of new products to production facility by assisting in the

development of process validation requirements (PFMEA, IQ, OQ, PQ) using appropriate

statistical tools and techniques.

• Review Design History Files and Technical Files for conformance to applicable

requirements

• Ensures applicability to SOUP / OTS validations in the product development

• Participate when appropriate in audits

• Participate and provide input to training on department / division procedures and policies

• Participate when appropriate in internal and supplier audits.

• Applies quality system regulations, applicable standards and guidance to multiple projects

• Applies quality system regulations, applicable standards and guidance to multiple projects

• Develops templates and training based on the quality system regulations, applicable

standards and guidance.

• Independently reviews all SW deliverables to ensure compliance with development process

and the standard.

• Delivers presentations to the QA organization on status and issues of assigned projects.

Delivers training to departments outside of QA.

Required Knowledge and Experience

Minimum 4-6 years of quality engineering experience or equivalence and overall 6-8 years of experience

Working knowledge of and auditing experience to the FDA Quality System Regulation, ISO 13485, and the Medical Device Directive.

Good verbal and written communication skills including protocol / report development and technical presentations.

Familiar with ISO 9001, ISO 13485, IEC 62304, ISO 14971, IEC 60601, 21 CFR part 820, 21 CFR part 11, EUMDR and product specific industry standards.

Root cause failure analysis.

Previous experience working in a cross-functional team environment.

Working knowledge of and auditing experience to the FDA Quality System Regulation, ISO 13485

Familiar with statistical software tools (Minitab, Stat Graphics, Statistical)

Familiar with DMAIC or DMADV(DFSS) methodologies

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package

A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.

Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people.

We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here (http://www.medtronic.com)

Welcome to our new Careers Site!

If you applied before July 22nd, please check your email for a notification from us providing you with instructions and a link to set up your new account and retain access to your current activity. If you do not see an email from us, please feel free to proceed with creating a new account.

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.

Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people.

We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

We change lives . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That’s who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.

We build extraordinary solutions as one team . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.

This life-changing career is yours to engineer . By bringing your ambitious ideas, unique perspective and contributions, you will…

  • Build a better future, amplifying your impact on the causes that matter to you and the world

  • Grow a career reflective of your passion and abilities

  • Connect to a dynamic and inclusive culture that welcomes the challenge of life-long learning

These commitments set our team apart from the rest:

Experiences that put people first . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.

Life-transforming technologies . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.

Better outcomes for our world . Here, it’s about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.

Insight-driven care . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.

This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here (https://www.e-verify.gov/employees) .

For updates on job applications, please go to the candidate login page and sign in to check your application status.

If you need assistance completing your application please email AskHR@medtronic.com

To request removal of your personal information from our systems please email RS.HRCompliance@medtronic.com

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