药物分析部助理主任(年薪15~20W)                                
Key Responsibility                                                         
                       
1.     Manage a technical group including multiple project groups and teams.
Assure the group/project teams to operate efficiently and effectively with 
high quality of services including on-time completion of projects, minimal 
yst’s error and full GMP compliance.                                   
                                             
2.     Communicate effectively and responsively with clients through email 
and tele-, web-, video- conferencing, and assure customer satisfaction.     
                                                                           
3.     Make project assignment and resource allocations, monitor the project
execution, follow up action plans, and track the project cost.             
                                                                   
4.     Lead a good functioning team with effective hiring, good supervisory 
and leadership skills, ability to motivate, and effective conflict 
management.                                                                 
               
5.     Lead, coach and train the ysts in the team to perform method 
development and validation, technology transfer, testing release and 
stability samples and OOS/OOT investigation with sound regulatory knowledge 
and understanding of GMP.                                                   
                             
6.     Write, review and approve technical documents including ROA, COA, and
method development and validation reports.                                 
                                               
7.     Manage the laboratory to be organized, clean, tidy, safe and full 
compliance with GMP requirements. Write and review SOPs to standardize the 
operations, and to improve operation efficiency and GMP compliance.         
                                                                       
8.     Perform cost estimate, set up project schedules and assist department
head to draft the quotations.                                              
                                  
9.     Communicate and interact with cross-functional teams and departments 
effectively.                                                                
                
10.   Performed all assigned work effectively and efficiently.              
                                                                  
Requirements:                                                              
          
                                                                            
     
1      Must have 5 or more years of industrial experiences in ytical R&D
                                                                            
    
2      Must be well familiar with the requirements of the FDA cGMP/GLP 
regulations, and ICH guidelines.                                            
                                    
M. S. or PhD in Chemistry, Pharmaceutical or related science degrees with 
direct experiences and training in ytical chemistry and pharmaceutical 
ysis including chromatography                                           
                                     
4      Must have supervisory experiences (group leader and above) in 
pharmaceutical ytical field.                                            
                                    
5      Must have strong communication skills, verbal and written, especially
in English, and interpersonal skills.                                      
                                          
6      Experiences in Pharmaceutical formulation support and stability 
programs are preferred.