Technical Editor
Santa Rosa, CA

Careers That Change Lives
This position will be responsible for ensuring quality and consistency in labeling and related technical documents. Help to align labeling with standard guidelines and documented procedures for master branding, medical device labeling regulations and standards, meeting all requirements as defined in labeling attributes master plans and product specifications.

CVG
The Cardiac and Vascular Group brings all of our cardiac and vascular businesses together into one cross-functional, collaborative operating unit to employ the full breadth of our talent, technologies, products, services, and solutions to address the needs of customers and patients across the globe.

A Day in the Life
Responsibilities may include the following and other duties may be assigned.

• Edit medical device labeling according to defined internal and external standards.
• Proofread English material; check grammar, spelling, consistency, clarity and compliance with internal and regulatory labeling requirements.
• Conduct quality check of multi-lingual labeling content to identify lack of consistency or irregularities in content.
• Provide substantive editing and proofreading for product labeling (e.g., product and package labels, product inserts, carton artwork, etc.) and documentation.
• Acquire and utilize product knowledge by working with labeling specialists, labeling designers, product developers, regulatory, quality, and marketing personnel and by referring to the product, the technical specifications and engineering documentation, and medical device standards and regulations.
• Maintain necessary records for project tracking and quality requirements.
• Collaborate and communicate with team members to ensure timely completion of projects.
• Provide input regarding labeling content.

Must Have: Minimum Requirements
To be considered for this role, please ensure the minimum requirements are evident on your resume.

• Bachelors Degree and 2+ years' experience in editing, proofreading, technical editing, or related field.
• Masters Degree and 0+ years experience in editing, proofreading, technical editing, or related field

• Experience in proofreading/editing labeling content for the medical device industry or regulated environment
• Working knowledge of medical terminology
• Experience with document management systems (e.g., Agile, Documentum, eMatrix)

About Medtronic
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.

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.

The physical demands described within the Day in the Life section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EEO
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees

Additional Information

• Posting Date: Nov 20, 2020
• Travel: No