Job Summary

A company is looking for a Regulatory Affairs Associate II.

Key Responsibilities:

• Assist with the development, implementation, and management of regulatory affairs compliance programs
• Coordinate and maintain regulatory submissions for domestic and international markets
• Track pending submissions and ensure timely execution

Qualifications:

• Bachelor's degree in Engineering, Life Science, or other technical discipline
• 2-8 years of related professional experience in regulatory affairs, preferably in medical devices
• Working knowledge of clinical laboratory and healthcare delivery system regulations
• Strong research, analytical, and problem-solving skills
• Ability to prioritize and manage multiple assignments within established time frames