Responsibilities:

• Report to the Quality Assurance Manager and work closely with the GroupProject Team;  
• Provide technical, organizational and document development assistance during daily operations; 
• Ensure that validation procedures are followed and templates are consistently utilized to generate qualification documentation for manufacturing and process equipment, facility and utility systems;  
• Prepare validation documentation in a timely and compliant manner;  
• Provide support for various qualification activities within the project life cycle, including the preparation of validation documents and the potential execution of qualification studies; 
• Support the validation programs by understanding and applying procedures and policies in the generation of documents which are fully compliant with internal standards, procedures and regulatory agency requirements;  
• Establish, implement and revise procedures/ validation documents. 

 Requirements:

• Bachelor degree in chemical / mechanical engineering or pharmaceutical, chemical science or biological related science discipline;  
• Experience in pharmaceutical industry is an definite advantage, candidates with more experiences will be considered as Senior Validation Engineer;
• Possess knowledge of validation protocol and documentation practices;  
• Proficiency in PC applications, including MS Office;  
• Attention to details, self-motivated, flexibility in working, interacting and communicating with diverse individuals/groups

APT Pharma Limited is a leading pharmaceutical manufacturer in Hong Kong. APT Pharma Limited also followed Good Manufacturing Practices. The Company has its manufacturing plants based in both Hong Kong and Zhongshan. We are now looking for a high calibre individual for the following position: