Overview
Join to apply for the Document Control Specialist 2 role at Dexcom.
Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom is committed to improving human health by empowering people to take control of their health through personalized, actionable insights. We are driven by a culture of integrity and a focus on solving important health challenges, with opportunities to grow globally.
Dexcom is an equal opportunity employer. We value diverse perspectives and are committed to creating an inclusive environment for all employees.
Responsibilities
* Manage the change control system, review, route, and release change orders.
* Assist in change control system software training and other training as required.
* Ensure projects are completed accurately and on time.
* Interact with internal and external customers.
* Support Quality in both external and internal audits.
* Monitor the status of in-process document changes to ensure timely revisions.
* Assist customers with problem solving and provide solutions using job knowledge and skills.
* Scan, archive, and retrieve quality documents and records.
* Issue controlled and uncontrolled documents.
* Maintain service records of all departments.
* Prepare requests for reproduction of documents.
* Maintain external standards in accordance with standard operating procedures.
* Support the development of documentation and configuration control procedures.
* Support the testing and improvement of the change control software and other supporting software.
* Generate Quality Assurance reports as needed.
What Makes You Successful
* Minimum of 2 years related experience and/or training; or equivalent combination of education and experience.
* Proficient with Microsoft Office Suite.
* Ability to create reports in support of other Quality Assurance systems.
* Ability to use critical thinking and resolve issues.
* Knowledge of electronic documentation systems.
* Good understanding of Document Control requirements and processes as outlined in ISO 13485 and 20 CFR part 820.
* Ability to apply acquired knowledge of GDP and GMP to daily tasks.
* Able to support rotating shift.
What You’ll Get
* A front row seat to life-changing CGM technology and a collaborative team environment.
* Comprehensive benefits program.
* Growth opportunities on a global scale.
* Access to career development through in-house learning programs and/or qualified tuition reimbursement.
* An innovative, industry-leading organization committed to its employees, customers, and communities.
Experience And Education
* Typically requires a minimum of 2-4 years of related experience and a school diploma/certificate or equivalent.
Note: This description reflects the current responsibilities and requirements for the role and may be subject to change.
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