Job Title: Regulatory Affairs Associate
About the Role:
Our organization is seeking a highly motivated and experienced professional to fill this key role in our regulatory department. As a member of this team, you will be responsible for ensuring compliance with international regulatory requirements.
Responsibilities:
Support day-to-day regulatory activities, including handling multiple projects related to compliance enhancements. Assist in implementing global quality management systems to regulations. Work closely with interdisciplinary team members to ensure the effectiveness of our product development and commercialization processes. Monitor global trends and requirements impacting product development and commercialization. Evaluate changes for regulatory impact and maintain awareness of global legislation.
Requirements:
Bachelor's degree in Engineering or Science with a minimum of 3 years of experience in regulatory affairs within the medical device industry. Certifications in EU MDR and US FDA desirable. Proven track record with ability to successfully manage projects to deadlines. Experience working directly with regulatory agencies.
Working Hours:
Full-time position.
What We Offer:
Competitive salary and benefits package. Excellent opportunity to develop your career in an exciting field.