Các Phúc Lợi Dành Cho Bạn
Mô Tả Công Việc
- Set up validation equipment plan. Perform OQ, PQ for equipment
- Evaluate equipment quality and suggest inappropriate equipment handling
- Do a risk assessment related to the manufacturing equipment system
- Participate in error handling and implementation of CAPAs related to equipment
- RO system validation
- Participate in computer system validation
- Development of HVAC auxiliary system validation plan.
- Validation compress air
- Do a risk assessment related to the auxiliary system
- Develop SOPs for auxiliary system
- Take part in handling deviation related to HVAC systems, compress air, RO system
- Check production area GMP compliance
- Responsible, complete the work assigned from the room manager
- Report the work to the direct manager
Yêu Cầu Công Việc
Bachelor degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Engineering.
PROFESSIONAL KNOWLEDGE & SKILLS:
- 4 years of experience in pharmaceutical factory.
- Ability to work under pressure
- Understanding the auxiliary systems in pharmaceutical production
- Understanding pharmaceutical manufacturing equipment
- Ability to analyze and solve problems
- Understand the systematic process of GMP-WHO, GMP-EU in the pharmaceutical industry.
- English : Listen, speak, translate documents well
- Microsoft Excel-Word, Autocad
- Be careful, honest.
- Ability to interact with colleagues at all levels throughout the company.
- Support other departments at work