Data Entry Clerk

Join Our Team as a Data Entry Clerk for MDR Remediation - 50 Exciting Openings!

Are you detail-oriented, reliable, and eager to make a meaningful impact in the healthcare industry? We are seeking motivated Data Entry Clerks to support a critical MDR Remediation project in the North Chicago suburbs. This is a unique opportunity to be part of a high-stakes effort to ensure regulatory compliance with the FDA's requirements, contributing to patient safety and medical device integrity. Whether you're just starting your career or looking to gain valuable experience in a regulated environment, this role offers a chance to grow, learn, and make a difference.

What You'll Do:
In this vital position, you will review, enter, validate, and maintain high-quality data related to Medical Device Reports (MDRs), regulatory submissions, and compliance documentation. Your attention to detail will help ensure accurate data entry, supporting audit readiness and regulatory compliance. You'll collaborate with cross-functional teams, assist in data reconciliation, and help prepare documentation for FDA inspections-all while working in a fast-paced, team-oriented environment.

Required Skills:

• Strong attention to detail with a focus on accuracy
• Ability to follow structured processes and work with regulated data
• Basic computer skills, including proficiency with Microsoft Excel and data entry systems
• Good organizational and time-management skills
• Capacity to handle repetitive tasks with consistency and focus

Nice to Have Skills:

• Prior experience in data entry, records management, or administrative support
• Familiarity with MDR processes, FDA regulations, or quality management systems
• Experience working in regulated environments such as healthcare, pharmaceuticals, or medical devices
• Knowledge of ERP, CRM, or document management systems

Preferred Education and Experience:

• High school diploma or equivalent (associate degree or higher preferred)
• Experience in data entry, administrative roles, or regulatory support is advantageous
• Previous work in regulated settings is a plus but not mandatory

Other Requirements:

• Ability to work 40 hours per week with 3 days onsite and 2 days remote
• Capability to pass a drug screening and background check
• Willingness to support project deadlines, with the key deadline being October 20th for data upload submission

Ready to embark on a meaningful career journey? Apply now and become a vital part of a team dedicated to compliance, safety, and excellence in medical device reporting!

Dexian, LLC is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.

Dexian stands at the forefront of Talent + Technology solutions with a presence spanning more than 70 locations worldwide and a team exceeding 10,000 professionals. As one of the largest technology and professional staffing companies and one of the largest minority-owned staffing companies in the United States, Dexian combines over 30 years of industry expertise with cutting-edge technologies to deliver comprehensive global services and support.

Dexian connects the right talent and the right technology with the right organizations to deliver trajectory-changing results that help everyone achieve their ambitions and goals.To learn more, please visit https://dexian.com/.

Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.