Key Roles and Responsibilities

• Manage the development of new products by transforming new ideas, designs and technologies into commercial success;
• Liaise closely with different departments including R&D, production, QA, QC, regulatory affairs, sales and marketing with regards to product development and market development;
• Monitor project timeline and ensure project milestones can be achieved according to the schedule;
• Provide solution to technical problems and handle Europe CE mark application.
• Prepare to participate in other drug development projects.

Qualifications and Experience

• Post graduate degree in mechanical engineering, life science or pharmaceutical related disciplines;
• Proven track record in managing medical device design and development projects, preferably in in-vitro diagnostic devices;
• Solid knowledge in ISO 13485 and ISO 14971 or equivalent quality standards recognized by European health authorities;
• Experience in handling Europe CE mark application;
• Strong leadership and communication skills.
• This is a 2-year contract role based in Hong Kong. Upon completion of the contract, successful candidate will be offered a permanent role

How to Apply

You are invited to send in your application and CV stating the position with reference number JGM2003-011 or mail Room 2313-18, Tower 1, Millennium City 1, 388 Kwun Tong Road, Kwun Tong, Kowloon on or before 16 April 2020.

Jacobson Group Management Limited is an Equal Opportunities Employer. Personal data provided by job applicants will be used strictly in accordance with our personal data policy and for recruitment purposes only. We aim to respond to successful applicants within 8 weeks and related information will be kept in our file for up to 12 months for other suitable vacancies in our organization and thereafter destroyed.