Job Description

Roles and Responsibilities

1. Support the quality and regulatory team in Health products (medtech, pharma, cosmetic) projects.

Project such as:

Quality management system preparation and implementation for certification eg ISO 13485, GDP, ISO 9001 for health products manufacturer and/or distributor such as design control procedures, manufacturing process, distribution procedures Product registration with country dossier preparation from the product technical documentation & Quality Management system for Singapore HSA, CE, and global registration.
2. Support company administrative activities assigned to team related to health products business.

3. Support on marketing, sourcing, and control management of resources (business, financial, human resource, facility)

4. Support in projects by understanding client needs, strategy planning, preparation of required documents or sourcing of information, tracking of status and communication to client for timely completion of projects.

Project such as:

Business process documentation preparation and implementation Marketing information related to medical device Quality management system preparation and implementation for certification Product technical documentation preparation Product registration with country dossier preparation for world-wide submission, including new products, change/variation & renewals to the relevant authorities

Requirements/Qualifications

Diploma/Bachelor Degree in Science, Engineering, Business or related fields. Minimum 1 year experience. Skills - Technical Documentation, Regulatory, Quality Management, GMP, Design Control, Business Process
Job Type: Full-time

Pay: $2,500.00 - $3,500.00 per month

Work Location: In person