Medical Device Regulatory Affairs Consultant (medlance.co)

Join our dynamic MedTech team as a Medical Device Regulatory Affairs Consultant and play a pivotal role in navigating the complex regulatory landscape. We are looking for experienced professionals who can provide strategic guidance and support for regulatory submissions, compliance, and product registrations.

Responsibilities:

• Guide Medical Device companies through the regulatory process.
• Prepare and submit documentation for FDA and other regulatory bodies.
• Ensure compliance with all regulatory requirements.
• Collaborate with cross-functional teams to address regulatory issues.

Qualifications:

• Proven experience in Medical Device Regulatory Affairs.
• Strong knowledge of FDA regulations and international standards.
• Excellent communication and organizational skills.
• Ability to work independently on complex projects.

Benefits:

• Flexible remote work.
• Access to a vast network of MedTech companies.
• Competitive compensation.
• Opportunity to work on diverse and challenging projects.

How to Apply: Create a profile and apply through MedLance at https://medlance.co/

Job Type: Contract

Pay: $30.00 - $300.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Flexible schedule
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• Choose your own hours

Experience:

• Medical Device Regulatory Affairs.: 3 years (Required)

Work Location: Remote