Formulation Process Facilitator - Taizhou, 中国 - AstraZeneca

描述

Job Responsibilities:

-Supervise all production activity meet the requirement of GMP and company standards.
-Schedule detail production activity to ensure the production plan was fulfilled.
-Investigate and rectify deviation during granulation
-Optimize process to keep Production efficiency and result
-Check and release the BPR
-Issue and update the relative SOPs to supervise the production activity
-Supervise production document management
-Perform equipment Validation & Re-validation activity.
-Co-ordinate and support the maintenance and repair.
-People line Management

-Manage the position training system to ensure people qualification meet the position requirement
-People management and development

-Participate the business project needed

-Establish and maintain good relationship with suppliers of equipment for business needs

-SHE responsibility

-GMP requirements

-Regulatory Compliance

Job Requirements:

-Bachelor degree with pharmaceutical related background

-Pharmaceutical production knowledge
-Good manufacturing Practice
-People management skill

-3 years of management working experience related pharmaceutical industry

-Good English in reading, writing, speaking

-Good application of office software

-Good communication skills and teamwork coordination
- Good management skills
- Production Problem solving

Date Posted

Closing Date