Greetings from VDart!!!

I would like to know if you are looking for this opportunity at this point of time? Let me know your comments

Role: IB-Regulatory Engineer - Medical Devices Regulations

Location: Waukesha WI (Onsite)

Type: Contract

The team developing industry leading X-ray generation subsystems is looking for highly motivated regulatory engineers to join them in ensuring compliance and availability of these subsystems for CT scanners to all the global markets of interest.

Regulatory Engineer will be working on compliance activities for various medical devices global regulations.

Responsibilities

• Collaborate with cross functional teams (engineering, manufacturing, regulatory, sourcing, etc.) to lead or support compliance activities to medical device regulations.
• Review regulatory compliance change notifications and drive associated actions to be compliant by the effective date
• Lead compliance efforts to various global regulations (E.g. REACH, ROHS, etc.) in alignment with the quality management system
• Lead or support product regulatory documentation updates (e.g. NRTL reports, tech file, etc.)
• Support regulatory audits and inspections to ensure post-market surveillance compliance.

Qualifications we seek in you!

Minimum Qualifications

• Knowledge of medical regulations including FDA, EU MDR, NMPA/CFDA, and other applicable international regulations
• Knowledge of regulatory standards such as IEC 60601, ISO13485, 14971 and other applicable standards and substandard.
• Proficiency in interpreting, applying complex regulations, and preparing associated documentation.
• Excellent interpersonal communication and collaboration skills
• Bachelor’s degree in engineering, Science or related area
• Minimum of 2 years of experience working with medical devices regulations and quality management system.

Regards

Gowtham Chandrasekar

Senior Recruiter

Contact: (470) 750-9953

Email: [email protected] 

Website: https://www.dimiour.io/