Global Regulatory Affairs Specialist – Medical Devices

Experis Technology Group; Eagan (MN); On-site; USD 25,000 - 30,000; Full time

Benefits offered by this job

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

Health Savings Account

Health Flexible Spending Account

Dependent Care Flexible Spending Plan

Supplemental Life Insurance

Short Term Disability Insurance

Long Term Disability Insurance

Business Travel Insurance

401(k) with Match

Weekly Pay

Job summary

Experis Technology Group is partnering with a global healthcare organization to recruit a Regulatory Affairs Specialist for an onsite, 12-month contract in Eagan, MN. You will contribute to regulatory affairs efforts supporting global product registrations and labeling changes for medical devices and some drug products.

Ideal candidates hold a bachelor’s degree in a technical field, have at least 1 year in regulatory affairs for medical devices, and can support international registrations.

Qualifications

• Bachelor’s Degree or higher from an accredited university in a technical field such as Biology, Chemistry, Pharmacology, Biochemistry, or similar.
• Minimum 1 year of regulatory affairs experience in the medical device industry.
• Experience supporting international registrations.
• Proficiency with Microsoft Office applications, including Excel and Word.
• Spanish language proficiency preferred.

Responsibilities

• Contribute to regulatory affairs efforts that support global product registrations and labeling changes for medical devices and some drug products.
• Work with the international regulatory affairs group to help ensure products are registered globally in alignment with the spinoff strategy.
• Create, maintain, and update RegDesk tracking records for the rebranding project.
• Support regulatory documentation and compliance-related tasks as assigned.
• Collaborate with internal stakeholders to evaluate information accurately and help ensure regulatory alignment.

Skills

Regulatory affairs

International registrations

Attention to detail

Education

Bachelor’s degree or higher in a technical field

Tools

Excel

Word

Job description

Experis Technology Group is partnering with a global healthcare organization to recruit a Regulatory Affairs Specialist for an onsite, 12-month contract in Eagan, MN. You will contribute to regulatory affairs efforts supporting global product registrations and labeling changes for medical devices and some drug products.

Ideal candidates hold a bachelor’s degree in a technical field, have at least 1 year in regulatory affairs for medical devices, and can support international registrations.