Job Responsibilities

- Primary responsible for documentation support.
- Handle document change control of web-based document control system (Product Data Management/Teamcentre system).
- Working knowledge of document change control process in a medical devise and/or pharmaceutical industry is required.
- Administer web-based training system (SABA)
- Administer document archiving, retrieving and destruction process
- Support Quality training initiative and other administrative support.


Job Requirements

- Diploma in quality or engineering and at least 3 years of direct medical device/pharmaceutical experience is required
- Knowledge in GMP is preferred / Proficiency in Microsoft Office
- Good verbal and written communication skills are required
- Strong organizational, prioritization and task planning skills


Note: Only Singaporeans and Singapore PR need apply

Interested candidates with above qualifications, please forward detailed resume in MS Word format to: xx_xxxxxx@xxxxxxxxxx.xxx.xx and to include information on the following:

1) Indicate the Position apply for
2) Reasons for leaving current and/or last employment
3) Last drawn and/or current salary
4) Expected salary
5) Date of availability and/or Notice Period
6) Recent photograph

Call your Professional Executive at Tel: 6438 2886 for more details

All applications will be treated in strictest confidence and only short-listed candidates will be notified.

It is unlawful to employ a person who does not have permission to live and work in Singapore. Unless the advert states otherwise, please ensure you have this permission before applying.