Jobs
Benefits & Perks
•Healthcare
•Dental
•Vision
•Health Savings Account
•Life insurance
•Long Term disability
•Tuition assistance
•401(k)
•Paid time off
•Paid holidays
•Employee Stock Purchase Plan
•Employee Assistance Program
•Healthcare
•401k
Required Skills
Quality engineering
Quality assurance
Root cause analysis
Statistical analysis
Regulatory compliance
Problem-solving
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
As a Quality Engineer in Manufacturing, you will play a key role in ensuring that products are manufactured in compliance with internal quality standards, regulatory requirements, and Medtronic’s commitment to patient safety and product excellence. This position partners closely with Manufacturing, Operations, R&D, and Supply Chain to drive quality improvements and support continuous improvement initiatives on the production floor.
Responsibilities may include the following and other duties may be assigned:
- Provide quality engineering support for manufacturing operations and engineering.
- Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs , supporting risk assessments, to ensure compliance with regulatory and quality system requirements.
- Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions.
- Collaborate with cross-functional teams to identify, assess, and mitigate quality risks in manufacturing processes.
- Support internal and external audits, including preparation, participation, and follow-up on audit findings.
- Drive continuous improvement initiatives using quality and lean methodologies.
- Ensure effective implementation and monitoring of process controls and quality metrics.
- Support change management activities ensuring requirements are identified and executed when applicable.
- Participate in Management Review and Quality Metrics reporting.
Required Knowledge and Experience:
- Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or a related field.
- Minimum of 7 years of experience in quality engineering or quality assurance of production in medical devices or pharmaceuticals.
- Knowledge of quality systems and regulatory requirements (e.g., ISO 13485, FDA QMSR, MDR).
- Strong analytical and problem-solving skills.
- Ability to work effectively in a cross-functional, fast-paced manufacturing environment.
- Hands-on experience with ECO’s, nonconformance management, CAPA, and root cause analysis tools.
- Familiarity with statistical tools and data analysis.
- Experience supporting audits and inspections.
- Knowledge of Lean, Six Sigma, or continuous improvement methodologies- advantage.
- Strong communication skills in English, both written and verbal.
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 95,000 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
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About Medtronic
Reviews
3.3
10 reviews
Work Life Balance
3.2
Compensation
4.0
Culture
3.4
Career
3.8
Management
3.5
65%
Recommend to a Friend
Pros
Great coworkers and supportive team
Good benefits and compensation
Growth and advancement opportunities
Cons
Aggressive leadership and cultural changes
Limited work-life balance in some roles
Company prioritizes profits over employees
Salary Ranges
1,888 data points
Mid/L4
Mid/L4 · Clinical Specialist
306 reports
$173,492
total / year
Base
$108,731
Stock
-
Bonus
$18,129
$110,237
$281,189
Interview Experience
6 interviews
Difficulty
2.5
/ 5
Duration
14-28 weeks
Experience
Positive 0%
Neutral 67%
Negative 33%
Interview Process
1
Application Review
2
Recruiter Screen
3
Technical Phone Screen
4
Technical Interview Round 1
5
Technical Interview Round 2
6
Final Interview
Common Questions
Technical Knowledge
Coding/Algorithm
Behavioral/STAR
Past Experience
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