Eastern District
Pharmaceuticals & Medical Devices (Healthcare & Medical)
Full time
Our client is a listed and well-known healthcare MNC. Currently they're hiring for a Senior Regulatory Affairs Specialist to join the medical team.
Responsibilities:
Responsible to submit registration dossier for both pharmaceutical and medical device to local authorities and obtain regulatory approvals
Support tender submission and manage change for both pharmaceutical and medical device product
Maintain the regulatory affairs databases up to date and assist in annual authority inspection
Interaction with local regulatory authorities, as well as inter-department coordination
Provide professional advice on regulatory strategy and prepare submission plan to support business
Requirement:
Bachelor’s degree in science or healthcare-related fields
Minimum of 5 years’ work experience of regulatory / quality in medical device or pharmaceutical industry
Good command of written and oral English, good command of spoken Chinese and Mandarin
Excellent communication and interpersonal skills and good team player
Immediate available will be an advantage
Please send your CV with expected salary and notice period to career6@stapacific.com