About this role
Regulatory Affairs Specialist at VB Spine. Location: Poland. Role: collaborate development, prepare submissions, coordinate agencies Requirements: Regulatory Affairs Specialist with 2+ years in medical device or pharma, English fluency, knowledge of FDA/EU regs, RAC preferred. Category: Legal and Compliance Seniority: Mid Level Tools: Microsoft Office Certifications: rac Commitment: Full Time Workplace: Hybrid Languages: English