Documentation Control Officer
5 months ago
1. Coordinate to ensure no overdue SOP in each area/ department
2. Control electronic and non-electronic documents so that only effective/ valid documents are located in the Cimanggis Site
3. Writing SOPs in Documentation area and updated in line with the newest version of related GSOP.
4. Ensure 100% CMS implementation in Documentation area.
5. Writing SOPs in Change & documentation area and updated in line with the newest version of related GSOP.
6. Ensure 100% CMS implementation in Change & Documentation area.
9. Support of internal and external audit in PT Bayer, Cimanggis Site performed in timely manner.
10. Ensure that CAPA as result of Documentation area are completely finished in timely manner.
11. Support maintaining appropriate precaution on occupational safety and health as well as security of facilities within Quality Department.
12. Upgrade her/his-self in management and professional skills and including developing team especially on GMP aspects
13. Support maintaining appropriate precaution on occupational safety and health as well as security of facilities within Quality Department.
**Specification**:
1. Bachelor degree in Pharmacy / Apothecary / Chemical Engineering / Industrial Engineering
2. 1+ years’ experience in GMP aspects or related with the food supplement or drug manufacturing/Fresh graduate still applicable.
3. Proficiency in oral and written in English
4. Understands and familiar with current GMP
5. Mastering computer operation for standard office
6. Have ability to create SOP and or other GxP documents
7. Have good skill in leadership and communication
8. Have good integrity
9. Have good initiative
**Job Types**: Full-time, Contract
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