about the company
A global medical technology company with over 85,000 employees, manufacturing devices and therapies to treat more than 30 chronic diseases. With over 50,000 patents, this global medical technology organization is dedicated to innovation and collaboration with educational institutions to transform and revolutionize care delivery. Often cited as the world’s largest stand alone medical technology company, this organizational giant is committed to recognizing the personal worth of employees by providing an employment framework that allows personal satisfaction in work accomplished, security, advancement opportunity, and means to share in the company's success.
about the job
As a regulatory affairs associate, you will be responsible for a range of critical tasks that include:
- Ensure products in development projects are in compliance with all internal and external regulatory requirements.
- Prepare filings of regulatory documents and implement regulatory submissions plan in line with product development objectives
- Being in control of change processes in ensuring compliance of products are in line with new regulations through supplying documentation.
about the manager/team
Reporting to the Regulatory Affairs Manager, you will provide full regulatory leadership across all product portfolio in Singapore, in achieving the organization’s business goals and objectives.
skills & experience required
To be successful in this role, you have a strong proven experience of at least 2 years in regulatory affairs management with knowledge of European and international regulations and standards covering medical devices.
To apply online please use the 'apply' function, alternatively you may contact Khalis at 6510 7401.
(EA: 94C3609/ R1551822)