Associate Quality Systems Specialist

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 **:We’re a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Work with us to incentivize better patient care, and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide.

As an Associate Quality Systems Specialist, you will have responsibility for development of and maintenance of quality programs focusing on Document Control. Our Global Quality Strategy is rooted in the Medtronic Mission and our Quality Policy. Being a 'trusted partner' means always putting patient safety first, upholding product quality, and maintaining the highest ethical standards in our business relationships and programs. The position will be fully remote.
**Responsibilities may include the following and other duties may be assigned**:

- Perform maintenance and oversight and implementation of Quality Management System Processes specifically for document control across Eurasia and Americas region in a form of centralized shared provision
- Prepare reports and/or necessary documentation and provides to applicable stakeholders, both internal and external
- Report includes data analysis, recommendations and suggestions to benefit improvement of process being supported
- Collaborate across multiple nationality within Medtronic to effectively implement document control process as well as identify areas for improvement and standardization for lean process implementation
- Analyze data to identify trends and opportunities to be used as baseline for improvement on quality aspects

**Required Knowledge and Experience**:

- Bachelor’s degree
- One year experience related to Quality, Regulatory, Compliance, or a related field
- Fluent in English
- Strong communication and interpersonal skills
- High attention to detail and accuracy
- Knowledge with Microsoft Office tools

Experience with Agile Systems/Tools and other Product Lifecycle Management (PLM) Systems. Proficient in ISO standards, including ISO 9001:2015 and ISO 13485:2016. Demonstrated experience in Quality Assurance and Quality Management Systems is highly advantageous.

**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.