Specialist

Detailed Job Description

1. Ensure that all Production activities in J-II & J-VIII are complying with Local Regulatory and Julphar EHS requirement. 
2. Ensure that all Production activities in J-II & J-VIII run in safe condition by ensuring that all safety measurement are sufficient, in place and in use  
3. Ensure that all Production activities in J-II & J-VIII are complying with Quality global standard, Regulatory requirements and Julphar cGMP/ GxP Polices. 
4. Ensure that all Production activities in Julphar J-II & J-VIII are running as per cGMP requirement by ensuring that all Quality measurement, and quality control strategy such as CCS (Contamination control strategy) are effective & efficient also in place and in use. 
5. Manag QMS related activities in J-II & J-VIII, Like CAPA implementation, Change actions as well and other related actions.  
6. Manage Monthly J-II & J-VIII plan to issue includes reviewing applicability, visibility and availability of resources and materials.  
7. Follow up on Daily Production plan Progress includes review productivity performance related issue and related measurement  
8. Management Problem solving sessions and activities for resolve Supply and Productivity obstacles 
9. Cooperate with Supply team for achieve maximum productivity plan by preparing the best plan setup with complying with Sales orders and urgency   
10.  Report any supply issues which may impact J-II & J- VIII delivery plan.  
11. Cooperate with Central packaging Value stream for achieve production plan .
    
    
    Qualification/Functional  Knowledge
     

1. Bachelor in pharmacy with 3 Year experience or high school with 6 Year experience.
2. Functional knowledge of pharmaceutical industry, understand the aseptic process.
3. Knowledge with cGMP principles and Aseptic filling Behaviour.