Regulatory Affairs Consultant (MedTech)

Role: Medical Devices Regulatory Consultant

Key Responsibilities:

• Provide regulatory strategy and guidance for medical device products across global markets.
• Prepare and review regulatory submissions (e.G., 510(k), CE Mark, MDR/IVDR, and other regional filings).
• Ensure compliance with applicable regulatory requirements (FDA, EU MDR, ISO standards).
• Support product registration, regulatory documentation, and lifecycle management activities.
• Collaborate with cross-functional teams including R&D, Quality, Clinical, and Manufacturing.
• Monitor regulatory changes and assess impact on ongoing projects.

Requirements:

• 5+ years of experience in medical device regulatory affairs.
• Bachelor's degree or higher in Biomedical Engineering, Life Sciences, Medical Technology, Pharmacy, or a related discipline