Regulatory Labeling Specialist | Medical Device 12-Month+ Contract | 1st Shift | Monday-Friday, 8:00 AM-5:00 PM Support Regulatory Compliance and Patient Safety Through Accurate Medical Device Labeling Our client, a global leader in the medical device industry, is seeking a Regulatory Labeling Specialist to support the creation, revision, and implementation of product labeling. This role focuses on labeling design, document control, and regulatory compliance while collaborating with Regulatory Affairs, Quality, R&D, Engineering, and Manufacturing teams. Key Responsibilities Create and revise medical device labeling using approved templates, style guides, and labeling software. Maintain labeling documentation, including drawings, specifications, change orders, and technical records. Ensure labeling accuracy and compliance with GMP, QSR, and internal quality requirements. Support labeling design using GLS/Prisym, Adobe products, and Microsoft Office. Operate Zebra label printers, barcode graders, and related equipment; troubleshoot printing issues as needed. Coordinate labeling verification, reviews, approvals, and production implementation. Maintain accurate records within PLM and document control systems. Update SOPs, work instructions, forms, and technical documentation. Collaborate with Regulatory Affairs, Quality, R&D, Packaging Engineering, and Operations to resolve labeling issues. Track project deliverables and support continuous improvement initiatives. What We're Looking For Bachelor's degree required. Experience creating or modifying labels using software such as Prisym, BarTender, NiceLabel, EasyLabel, or similar platforms. Experience within the medical device industry. Experience operating Zebra label printers or similar labeling equipment. Proficiency with Adobe Creative Suite, including InDesign, Photoshop, or Illustrator. Experience with CAD or SolidWorks. Strong attention to detail, organization, and documentation accuracy. Ability to follow established procedures and work within a regulated environment. Preferred Experience Medical device labeling development and change control. GMP, QSR, and quality system documentation. PLM or electronic document management systems. Barcode verification and labeling validation. Cross-functional collaboration with Regulatory Affairs, Quality, and Manufacturing. Why Consider This Opportunity? 12-month+ contract with a global medical device organization. Consistent first-shift schedule, Monday through Friday. Opportunity to support medical device labeling and regulatory compliance. Collaborate with engineering, regulatory, and quality professionals. Contribute to labeling accuracy, product quality, and patient safety. If you have experience with labeling software, medical device documentation, and regulated manufacturing environments, we encourage you to apply!

Pay:

$40.00 - $44.00 per hour Expected hours: 40.0 per week

Benefits:

401(k) Dental insurance Employee discount Health insurance Life insurance Vision insurance

Work Location:

In person