Job Description
The Regulatory Affairs Specialist shall provide technical support to legal and registration activities of the RA Department in compliance to the regulatory requirements as mandated by specific regulatory agencies.
Qualifications:
At least 1 to 2 years of working experience in the related field
Willing to do field work
Preferably with experience on FDA registration preferably both medical device and pharma
Qualifications:
At least 1 to 2 years of working experience in the related field
Willing to do field work
Preferably with experience on FDA registration preferably both medical device and pharma