Mclaren Consultancy

We are excited to announce an exceptional opportunity for an Assistant Regulatory Affairs Manager to join our Client's esteemed organization under the supervision of the Sr. Director, Regulatory Affairs. As a key member of their team, you will have the unique responsibility of overseeing regulatory affairs and product registration across the dynamic HK-APAC region.

Responsibilities:

• Take ownership of regulatory affairs and product registration for medical devices in Hong Kong and APAC regions. 

• Manage and ensure compliance with all regulatory requirements and activities.

• Collaborate closely with the Headquarter team to meet deadlines and adhere to product registration timelines. 

• Stay abreast of the latest trends and developments in regulatory affairs driving the organization's continued compliance.

• Foster excellent communication and relationships with external stakeholders and internal teams. 

• Maintain accurate and up-to-date documentation and records. 

Requirements: 

• A Bachelor's Degree or above in Medical or Life Science-related disciplines. 

• Solid experience in regulatory affairs, preferably gained from the medical device industry.

• Regional regulatory affairs experience in APAC countries is highly advantageous. 

• Excellent communication, organizational, and problem-solving skills. 

• Good command of both written and spoken English. 

• Immediate availability is preferred. 

Ready to join a dynamic team and become an integral part of a prestigious organization's growth and success? With our Client, you will have the opportunity to enrich your skillset, make a meaningful impact, and thrive within a collaborative and supportive work environment. 

We eagerly anticipate reviewing your application and helping you find your dream job. Apply today! Successful candidates will be contacted with two working days.