Mô tả công việc
1. Compiling specification for finish products.
2. Perform test in accordance with the approved SOPs or validation protocols to products (intermediate product, finished product, retained product, complaint product)
3. Follow up maintenance and calibration for laboratory equipments.
4. Compile and revise SOPs
5. Support to control reference standard/ working standard using in laboratory
6. Follow up and report for finished product stability.
7. Training for employees
8. Report promptly any abnormalities about quality to QC manager and other departments.
9. Participate in other works in QC Dept., follow the assignment of QC manager.
Yêu cầu
Bachelor's degree in Chemical Engineering/ Pharmacy/ Biotechnology
Fluent English
Good at MS Offices
Quyền lợi
Probation: 2 months of probation with full salary
Working time: 44 hours/week
Training:
A2E skill training
Pre-mortems
Prioritization
Problem solving
Owner's mindset
Idea generation
Coaching
Influencing
Courageous conversations
Effective communication
Presenting with impact
Closed-loop conversations
Creating business value
Effective meetings
Effective emailing
Organizational health
Colleague: Friendly, supportive
Annual Leave:
- 15 working days: from full 1 year to less than 3 years;
- 16 working days: from full 3 years to less than 7 years;
- 22 working days: from full 7 years or more to less than 37 years.
Benefits:
Japanese Health Insurance for Staffs over 2 years contribution
Company trip, Team building activities
Holiday events
Others:
Company bus from HCMC to Factory
Parking fee
Meal allowance
Thông tin khác
Thời gian làm việc
Thứ 2 - Thứ 6 (từ 08:00 đến 17:00)
Thứ 2 - Thứ 6 (08h00 - 17h00); Thứ 7 cách tuần
Thông tin chung
Nơi làm việc
- - Hồ Chí Minh: 16 VSIP đường số 5, KCN Việt Nam - Singapore, Phường Thuận Giao