Job Description / Requirements
JOB DESCRIPTION
Qualtech Manila Consulting Corporation is currently looking for a full-time Regulatory Affairs Associate.
The candidate will be mainly responsible for supporting the immediate supervisor in executing product registration activities. He shall also assist in catering to the in-country representation needs of clients.

KEY RESPONSIBILITIES
 Ensures effective presentation of technical dossier to regulatory agencies.
 Manages product certificates and performs other tasks related to in-country representation of principals.
 Develops & maintains updated knowledge of applicable international/regional and local regulations and guidelines.
 Performs other duties and responsibilities as may be assigned from time to time.

Location: Makati

MINIMUM QUALIFICATIONS
Bachelor’s degree in Pharmacy or related field from a reputable university
Minimum 1 years of regulatory experience, preferably in the pharmaceutical or device industry
Proficient in English

Salary : to be discussed
Industry : Research
Company Size : 10-50 Employees
Language : English
Dress Code : Business Casual
Benefits : Medical, Bonus
Working Hours: Mondays-Fridays 9am – 6pm

Company Overview:
Qualtech is a Medical Device Consulting Company, with over 15-year experience serving clients worldwide, specializing in China and Taiwan medical device clinical research. Recognized widely for our professional knowledge and management excellence, Qualtech continues to offer the best solution to our clients.

How to Apply
HOW TO CONTACT US Please send your CV to pamela@qualtechs.com. For faster processing, please be sure to include your FULL NAME/DESIRED POSITION on the subject title.