Full-Time

Senior Quality Engineer

Posted on 8/18/2026

Medtronic

Medtronic

10,001+ employees

Medical device maker advancing therapies

No salary listed

Hyderabad, Telangana, India

Hybrid

Flexible work arrangement.

Bachelor's

Category
QA & Testing (1)
Required Skills
Minitab
Six Sigma
GMP

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Requirements
  • A bachelor's degree in Engineering, Science, or a Technical Discipline is required.
  • A minimum of 8 to 12 years of quality systems experience is required.
  • Supplier management experience is an advantage.
  • Strong oral and written communication skills are required.
  • Ability to comprehend principles of engineering, physiology, and medical device use is required.
  • Previous customer-facing or project management experience is a plus.
  • Ability to work with international and multicultural departments and groups across different time zones is required.
  • Ability to deliver accurate, high-quality work with a sense of urgency is required.
  • Ability to work well under pressure and maintain a positive, enthusiastic attitude is required.
  • Ability to work in a fast-paced environment and eagerness to learn and expand responsibilities and accountability are required.
Responsibilities
  • Qualify suppliers according to company standards and manage the approved supplier list in compliance with purchasing controls.
  • Initiate and drive supplier corrective action and preventive action and nonconformance reports for suppliers that do not meet company standards, and manage supplier change requests.
  • Assess supplier performance periodically and drive necessary continuous-improvement actions.
  • Establish processes and ensure that suppliers deliver quality parts, materials, and services.
  • Lead production part approval process execution with suppliers and ensure robust supplier process qualification and validation using installation qualification, operational qualification, and performance qualification methodology.
  • Monitor parts from acquisition through the manufacturing cycle and communicate and resolve supplier-related problems as they occur.
  • Develop and prioritize an auditing schedule to ensure designated suppliers are regularly audited for good manufacturing practices and quality standards.
  • Provide pre-market quality engineering support to new product development in partnership with component engineering and post-market supplier quality teams to deliver quality parts, materials, and services and prevent defects.
  • Collaborate with component engineers to develop and deliver product acceptance sampling strategies, approved supplier list coordination, supplier-owned quality deployment, process failure mode and effects analysis, measurement system analysis, control plans, statistical process control, and other relevant quality tools and methodologies for new and legacy products.
  • Define receiving inspection requirements and associated test method validation for internal Medtronic test methods.
  • Conduct audits to qualify suppliers for their intended business use.
Desired Qualifications
  • Previous experience working with global teams in aerospace, defense, medical device, or automobile industries.
  • American Society for Quality certification such as Certified Quality Engineer, Certified Supplier Quality Professional, or Certified Quality Auditor.
  • Working knowledge of standards, guidance, and regulations.
  • Hands-on experience with Minitab tools.
  • Exposure to auditing against Food and Drug Administration Quality System Regulation and ISO 13485.
  • Lean Six Sigma Green Belt or Black Belt.
  • Good interpersonal skills and ability to work effectively in a team environment and build strong working relationships.

Medtronic makes medical devices and therapies to treat chronic diseases, including implantables, sensors, and diabetes management tools. Its devices interact with the body to regulate or monitor functions, such as pacemakers delivering heart stimulation and neuromodulation devices sending electrical signals. The company differentiates itself through a long history of device development and a broad portfolio, expanded via acquisitions to access new technologies and markets. Its goal is to improve patient health outcomes by providing integrated medical technologies that help manage chronic conditions.

Company Size

10,001+

Company Stage

IPO

Headquarters

Fridley, Minnesota

Founded

1949

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Simplify Jobs

Simplify's Take

What believers are saying

  • FY26 revenue reached $36.4 billion; organic growth hit 5.8%, the best in ten years.
  • FY27 guidance calls for 6.75%-7.25% organic growth, showing management confidence.
  • Health Canada approved Affera in 2026, expanding Medtronic’s atrial fibrillation addressable market.

What critics are saying

  • The August 4, 2026 $88 million mesh verdict opens thousands of similar Covidien claims.
  • MiniMed priced at $20, below $25-$28, signaling weaker investor appetite for diabetes.
  • Affera must convert CE Mark wins into US volume before Boston Scientific and Abbott respond.

What makes Medtronic unique

  • Medtronic’s Cardiac Ablation Solutions grew 78% globally, led by Affera and PulseSelect.
  • MiniMed’s 2026 IPO keeps Medtronic controlling diabetes while simplifying the portfolio.
  • Forty-nine straight dividend increases signal durable cash generation and shareholder discipline.

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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

Growth & Insights and Company News

Headcount

6 month growth

1%

1 year growth

1%

2 year growth

1%
Yahoo Finance
Aug 19th, 2026
Bank of America backs Medtronic as cardiac ablation unit posts 78% growth

Bank of America has maintained a Buy rating on Medtronic with a $95 price target, citing expectations for strong fiscal first-quarter results when the medical-device maker reports on 1 September. The company finished fiscal 2026 with $9.8 billion in fourth-quarter revenue, up 6.6% organically. Medtronic's Cardiac Ablation Solutions division posted 78% global revenue growth and 124% growth in the US, gaining eight percentage points of market share. Bank of America analyst Travis Steed expects similar growth rates to continue, potentially pushing results toward the upper end of management's 6% to 6.5% organic revenue growth guidance. However, concerns remain about sustaining momentum. Bank of America estimates CAS currently adds about three percentage points to total growth, making an eventual slowdown significant.

The Mirror Democrat and Savanna Times-Journal
Aug 18th, 2026
Craif raises $33M to accelerate introduction of its urine-based cancer test to the U.S.

Craif raises $33M to accelerate introduction of its urine-based cancer test to the U.S. * 4 hrs ago SAN DIEGO, Aug. 18, 2026 (GLOBE NEWSWIRE) - Craif Inc., a bio-AI company developing a urine analysis platform for early detection of cancer and other diseases, today announced the close of its approximately $33 million* Series D, bringing total capital raised since the company's founding to roughly $88 million**. Craif will use the proceeds to strengthen its U.S. R&D, prepare for a reimbursement-driven launch of its non-invasive cancer test in the United States and advance its Japanese regulatory filing for a software-based medical device program targeting pancreatic cancer diagnosis. The financing was co-led by Granite-Integral, a joint venture between Granite Asia and Integral Corporation, and by Tauns Co., Ltd., one of Japan's largest makers of rapid diagnostic tests. Granite Asia is a Singapore-based investment platform managing about $10 billion across the Asia-Pacific region. Integral Corporation manages approximately $3 billion and was the first Japanese private equity firm to list on the Tokyo Stock Exchange. U.S. based Unreasonable and existing investor X&KSK also participated, alongside institutional and individual investors across Singapore, the United States and Japan. The round comprised approximately $30.7 million in equity and approximately $3.3 million in debt. Founded in Japan in 2018, Craif developed a urine-based cancer detection platform that uses artificial intelligence to analyze microRNA, small regulatory molecules whose discovery and biological significance were recognized by the 2024 Nobel Prize in Physiology or Medicine. Its flagship test, miSignal, is offered at more than 2,500 medical institutions and 4,500 pharmacies across Japan, with over 110,000 tests performed to date. Craif has published more than 90 peer-reviewed papers and conference presentations, including two independent publications demonstrating the early and accurate detection of pancreatic cancer. A clinical team built for the American market A key component of Craif's plans is scaling R&D at its newly opened San Diego laboratory, including a prospective clinical study of its urine-based test in pancreatic cancer. This is an indication where the clinical utility and the path to reimbursement are clear. A simple, non-invasive urine test could help clinicians decide who needs further workup and who can safely wait. To spearhead that work, Craif has appointed Nicholas (Nick) Bevins, MD, PhD, as chief medical officer. Dr. Bevins will lead the company's clinical development strategy to build the body of evidence necessary to meet reimbursement and regulatory requirements. Dr. Bevins holds a bachelor's degree in biochemistry from Columbia University, an MD and a PhD in neuroscience from the University of California, San Diego, and completed a residency in clinical pathology and laboratory medicine. He has published more than 40 peer-reviewed papers and abstracts. He is a board-certified clinical pathologist and has served as both chief medical officer and CLIA laboratory director at several biotechnology and diagnostics companies. Because offering laboratory-developed tests in the United States requires a CLIA-certified laboratory under the oversight of a qualified laboratory director, Dr. Bevins brings a rare combination of that qualification and executive responsibility for clinical and regulatory strategy. His appointment further accelerates Craif's strategic expansion as it now advances partnerships with 30 medical institutions across 15 states. The company established a U.S. subsidiary in 2022 and joined the JLABS incubator. In April 2026, Craif opened its bio-AI laboratory in San Diego, and CEO Ryuichi Onose relocated there to lead the U.S. business. Chief Financial Officer Takeo Mukai, who previously held finance and operating leadership roles at Medtronic and several U.S. healthcare companies, also joined this year as a local hire. Quote from Ryuichi Onose, CEO and co-founder, Craif "We started Craif in 2018 to solve cancer, a problem the whole world shares, with technology built in Japan. We have brought our test to more than 2,500 clinics at home, and we are approaching a regulatory filing in pancreatic cancer. I moved to San Diego to build our U.S. business myself, because the United States is the hardest and most important market to prove this technology. What we are building goes beyond a single cancer test. The earliest signals of many diseases show up in urine, and reading them is what Craif is really about. Cancer is the first step." Quote from Nick Bevins, Chief Medical Officer "I joined Craif because the company has built a differentiated platform, generated an extraordinary body of clinical evidence in Japan, and is committed to advancing science through rigorous data rather than hype. Urine will play an increasingly important role in the future of early disease detection because it offers a non-invasive window into human biology. I look forward to collaborating with the team to make this accessible to patients." Quote from CK Chuon, Partner & Co-Head, Granite-Integral "Cancer screening should be as simple as a routine check-up, not a procedure patients avoid. Craif has proven in Japan that a non-invasive urine test can detect cancer early and at scale, and we believe the same approach can unlock massive unmet demand in the United States. We are proud to co-lead this round as Craif brings that vision to the world's largest healthcare market." Quote from Masataka Nonaka, President & Representative Director, TAUNS Laboratories, Inc. "Serving as a co-lead investor in Craif's Series D means a great deal to Mycarrollcountynews. This round will accelerate Craif's R&D, its clinical development toward regulatory approval and its global expansion. As one of Craif's distribution partners for miSignal, Mycarrollcountynews also expect the funding to move both miSignal and the pancreatic cancer SaMD program now in development closer to real-world clinical use. Craif's urine microRNA analysis technology opens new possibilities in early cancer detection and more precise diagnosis, and Mycarrollcountynews want to see it reach as many patients and healthcare institutions as possible. TAUNS will continue to support Craif's growth over the long term. Through its partnership, Mycarrollcountynews intend to help bring next-generation diagnostics into practice and contribute to solving healthcare challenges in Japan and around the world." *Total round amount, including equity investment, financing, and the secondary transaction. ¥5.28 billion at an exchange rate of ¥160.72 = $33 million. The exchange rate used is July TTM: ¥ 160.72 per USD. **Cumulative equity investment, financing, and grants since founding. Total funding raised to date: ¥14.2 billion (approximately $88 million). About Craif Craif is a bio-AI company founded in 2018 that develops non-invasive tests for the early detection of cancer. Its platform combines proprietary biomarker detection from urine and other bodily fluids with AI to assess disease risk. Building on one of the world's largest urine datasets, Craif aims to create a urine analysis platform that detects a wide range of diseases early, with cancer as the first step. The company is based in Tokyo and operates a wholly owned laboratory in San Diego, opened in 2026. Learn more at craif.com. Forward-looking statements This release contains forward-looking statements about Craif's plans, clinical development, regulatory timelines, and business prospects. Actual results may differ materially from those expressed or implied. Craif undertakes no obligation to update these statements except as required by law. Media inquiries Craif USA, Inc.

Yahoo Finance
Aug 16th, 2026
Medtronic faces $88M hernia mesh verdict as Health Canada approves cardiac ablation system

Medtronic faces contrasting developments after a federal jury ordered it to pay $88 million in compensatory damages over injuries linked to Covidien hernia mesh in August 2026. The verdict represents a record settlement in the ongoing litigation. Meanwhile, Medtronic Canada secured Health Canada approval for its Affera Integrated Mapping and Ablation System, designed to treat atrial fibrillation and atrial flutter. The approval gives Medtronic a second pulsed field ablation platform alongside its existing PulseSelect system. The company's investment narrative projects $41.5 billion in revenue and $6.6 billion in earnings by 2029, requiring 4.5% annual revenue growth. Analysts estimate a fair value of $98.00, representing a 7% upside from current levels. However, cautious analysts forecast lower revenue of around $38.6 billion and earnings of approximately $6.2 billion by 2029, citing concerns over legal exposure and execution risks.

Yahoo Finance
Aug 16th, 2026
Medtronic wins Health Canada approval for Affera heart rhythm system

Medtronic has received Health Canada approval for its Affera Integrated Mapping System and Sphere-9 Catheter to treat atrial fibrillation and atrial flutter. The licence permits commercial use of Medtronic's combined pulse field and radiofrequency ablation technologies across Canada. The Affera system offers physicians an all-in-one mapping and ablation platform designed to support procedural efficiency and patient care. The approval represents a milestone for Medtronic's Cardiac Ablation Solutions division in the global atrial fibrillation treatment market. Medtronic, a US-based medical equipment company with a market capitalisation of approximately $115.9 billion, develops and sells device-based therapies to healthcare systems and clinicians globally. The approval extends Medtronic's cardiac ablation offerings from Europe and the US into Canada, where it will compete with Abbott and Boston Scientific.

MD+DI
Aug 14th, 2026
Abbott opposes consolidating 23 spinal cord stimulator injury lawsuits.

Abbott opposes consolidating 23 spinal cord stimulator injury lawsuits. Abbott is fighting consolidation of 23 spinal cord stimulation injury lawsuits, arguing each case involves unique injuries and devices. Claire Wallace, Senior Writer, Informa Markets - Engineering August 14, 2026 Abbott has expressed opposition to turning 23 personal injury lawsuits against the company to just one, which would be heard before the Central District of California. The medtech giant has filed a motion against the consolidation, opposing multidistrict litigation for suits brought against Abbott's spinal cord stimulation devices. Abbott joins other major players in the industry, including Boston Scientific and Medtronic, who are facing lawsuits over SCS devices. In an August 4 motion filed by Abbott, the company claimed that the 23 injury lawsuits did not all share a common cause of injury, so they all need their own discovery processes. According to Abbott, 13 of the 23 plaintiffs have injuries unique to them. Injuries mentioned in the lawsuits include cardiac issues, infection, battery and Bluetooth issues, blood clots, body aches, back spasms, batteries and wires poking out of the skin and strokes, and required surgeries to remove the implant. "Assessing plaintiffs' claims based on each of these injuries will require an individualized inquiry into the injury's potential cause," Abbott's notion says. "Inquiries complicated by plaintiffs' failure to identify any common defect, which leaves every aspect of plaintiffs' devices' design and manufacture on the table as the potential cause." Of the lawsuits, several do not mention what Abbott device they were implanted with, one individual was not implanted with an SDS device at all, but rather a different chronic pain implant, and two individuals allegedly filed conflicting lawsuits in two different districts. Of the 23 lawsuits, 14 also name FDA, claiming that Abbott should not have received premarket approval from the agency for its SCS devices. "We stand behind the safety, quality, and performance of our spinal cord stimulation systems. These technologies help manage chronic pain and provide meaningful relief, improving patients' overall quality of life," Abbott shared in a prepared statement. "They are highly regulated medical devices that have been approved and updated in accordance with federal law through the FDA's rigorous premarket approval and supplement processes. We strongly disagree with the allegations in the cases Plaintiffs seek to consolidate." A law firm representing some of the plaintiffs argues that Abbott wants to keep the suits separate because it is better for the company financially. "Uncoordinated litigation makes it much more difficult and burdensome on plaintiffs and the judiciary than it is for [Abbott]," a response to Abbott's motion reads. Lawyers for the plaintiffs also believe that all of the injuries brought forward in the lawsuit have common underlying causes, despite having different device models. Senior Writer, Informa Markets - Engineering Claire Wallace is a senior staff writer at Medical Device + Diagnostics Industry (MD+DI), where she covers key developments in the healthcare and medical device industry. With nearly a decade of journalism experience, she brings a deep understanding of the healthcare industry and a proven ability to connect with physicians, medtech leaders, and policy experts on the issues shaping care delivery today. She is committed to delivering nuanced coverage that helps industry professionals anticipate trends, understand regulatory shifts, and identify opportunities in an increasingly complex healthcare ecosystem. Before joining MD+DI, Claire spent three years at Becker's Healthcare as a writer and assistant editor, leading coverage on developments across orthopedics, outpatient care, cardiology, and gastroenterology that bridged perspectives from clinicians and healthcare executives. Her reporting background also includes lifestyle, political, and clean energy news, with bylines in various national and digital publications. Claire earned her bachelor's degree in Communications and Media & Screen Studies from Northeastern University, where she also minored in Political Science and Journalism. She holds a master's degree in Media Advocacy and is currently based in Chicago. Want more MD+DI in your search results? Editors' choice. Aug 20, 2026