Associate Quality Systems Specialist

at  Medtronic

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.

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.

• 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