Regulatory Affairs Specialist - Medical Devices (Onsite MN)

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

Benefits offered by this job

Medical plan

Dental plan

Vision plan

HSA

Health FSA

Dependent Care FSA

Life Insurance

Short/Long Term Disability

Travel Insurance

401(k) with match

Weekly pay

Job summary

ManpowerGroup's client in the healthcare sector is seeking a Regulatory Affairs Specialist to join the Regulatory Affairs team in Eagan, Minnesota. This 100% onsite role supports division-level regulatory operations, global product registrations, and labeling changes for medical devices and some drug products.

The ideal candidate will have a Bachelor's degree and at least 1 year of regulatory affairs experience in medical devices, with experience in international registrations and strong

Qualifications

• Bachelor's degree or higher in biology, chemistry, pharmacology, biochemistry, or related field.
• Minimum 1 year regulatory affairs experience in the medical device industry.
• Experience with international registrations and regulatory documentation.

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

Medical devices

International registrations

MS Office

Spanish

Education

Bachelor's degree

Tools

RegDesk

Job description

ManpowerGroup's client in the healthcare sector is seeking a Regulatory Affairs Specialist to join the Regulatory Affairs team in Eagan, Minnesota. This 100% onsite role supports division-level regulatory operations, global product registrations, and labeling changes for medical devices and some drug products.

The ideal candidate will have a Bachelor's degree and at least 1 year of regulatory affairs experience in medical devices, with experience in international registrations and strong