Senior Design Quality Engineer at Medtronic

Hyderabad, Telangana, India

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Medical DevicesIndustries

Requirements

B.E. or B.Tech degree
Minimum 6-8 years of quality engineering experience or equivalence, and overall 8-12 years of experience
Review New Product Introduction (NPI) and Released Product Management documentation for quality characteristics, including manufacturability, serviceability, testability, reliability, and product requirements
Hands-on experience with tools package release process for both Software & Hardware tools/accessories
Review non-product/off-the-shelf tools for products
Experience in software or hardware design transfer process for tools or products
Familiar with ISO 13485, IEC 62304, ISO 14971, IEC 60601, 21 CFR part 820, 21 CFR part 11, EUMDR, and product-specific industry standards
Previous experience working in a cross-functional team environment
Familiar with statistical software tools (Minitab, Stat Graphics)
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
Hands-on experience in SW anomaly evaluation and disposition, complaint investigation, NC/CAPA
Hands-on experience on Software Risk Management and Design Controls

Responsibilities

Review new and modified product design documentation for quality characteristics, including manufacturability, serviceability, testability, reliability, and product requirements
Capable of mentoring junior quality engineers in providing quality engineering support
Ensure that product development projects and changes to existing products are conducted in compliance with IEC 62304, FDA Quality System Regulations, EU MDR, and in-house standards
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 demonstrate software capability and maturity
Assist in the creation of verification and validation plans, protocols, and reports; oversee testing and analysis for standards and product requirements compliance
Ensure successful transfer of new products/tools to production facility by assisting in 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
Participate when appropriate in audits
Ensure applicability to SOUP/OTS validations in the product development
Participate and provide input to training on department/procedures and policies
Develop templates and training based on the quality system regulations, applicable standards, and guidance
Independently review all SW deliverables to ensure compliance with development process and the standard
Deliver presentations to the QA organization on status and issues of assigned projects; deliver training to departments outside of QA
Provide quality support to facilitate resolution of product complaints and/or safety issues
Provide support to the Regulatory Department in writing technical submissions

Skills

ISO 13485

IEC 62304

ISO 14971

IEC 60601

21 CFR 820

21 CFR 11

EUMDR

DFMEA

Design Controls

Risk Management

NPI

Software Design

Firmware

Design Transfer

Medtronic

Develops and manufactures medical devices and therapies

About Medtronic

Medtronic provides medical technology, services, and solutions to improve patient care. The company develops a variety of medical devices, including pacemakers, insulin pumps, surgical tools, and neurostimulation devices, which help diagnose, prevent, and treat chronic diseases. These products are used by hospitals, clinics, and healthcare professionals around the world. Medtronic stands out from competitors by investing significantly in research and development to create new products and offering additional services like training and patient management programs. The goal of Medtronic is to enhance patient outcomes and lower healthcare costs through its comprehensive range of medical solutions.

Fridley, MinnesotaHeadquarters

1949Year Founded

$3.2MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

Health Savings Account/Flexible Spending Account

Unlimited Paid Time Off

Paid Vacation

Paid Sick Leave

Paid Holidays

401(k) Retirement Plan

401(k) Company Match

Employee Stock Purchase Plan

Employee Assistance Program

Wellness Program

Risks

Emerging competitors like Fire1 threaten Medtronic's heart failure management market share.

Spine biologics market growth may attract new entrants, increasing competition for Medtronic.

Recent IPOs in medtech indicate rising competition, challenging Medtronic's market position.

Differentiation

Medtronic's diverse product range spans cardiovascular, diabetes, neurological, and surgical technologies.

The company invests heavily in R&D to drive innovation in medical devices.

Medtronic offers comprehensive services, including training and technical support, enhancing product value.

Upsides

Exclusive deal with Kuros enhances Medtronic's orthopedic portfolio and market share.

Growing spine biologics market offers expansion opportunities in spinal fusion and regenerative medicine.

Balloon catheters market growth aligns with Medtronic's recent product launches, boosting cardiovascular presence.

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