A Regulatory Affair & Quality Assurance Manager position from a global leading medical device company
Your new company Our clients holds a premier position within the medical device industry. With a brand that is recognized worldwide and strong presence in Asia Pacific region. They have excellent reputation for providing rich legacy of innovation and a robust pipeline of promising innovative technologies in endoscopy.
Your new role
Based in Hong Kong, this RA & QA Manager will be responsible for leading regulatory affairs activities associated with issues to meet regulatory and customer requirements. As the lead, you will support the implementation and maintenance of quality management system policies including ISOs and procedures to ensure compliance with relevant international standards and regulatory requirements.
What you'll need to succeed
To qualify, you will possess a degree in sciences, medicine, engineering, pharmacy, microbiology or relevant scientific disciplines (5 years+) Extensive medical device industry experience in Regulatory Affairs is essential, Senior Regulatory Affairs will be offered with a less work experience candidate.
Influencing and engaging you will possess excellent interpersonal skills with excellent written English and Chinese.
What you'll get in return
In keeping with such an opportunity a highly attractive remuneration package is available to the successful candidate.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV to firstname.lastname@example.org
If this job isn't quite right for you but you are looking for a new position, please contact Charles Cheang, Life Sciences Consultant, +852 2230 7422 for confidential discussion. #1221478
Healthcare & Medical
Talk to a consultant
Talk to Charles Cheang, the specialist consultant managing this position, located in Hong Kong
6604-06,66/F, ICC, 1 Austin Road West, West Kowloon