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Pharmaceutical Quality Control Manager

Fintel (USA) Limited

  • Company Industries:Others

Job Information

  • Post Date:2017-10-28
  • Career Level:Senior
  • Location:Not Specified
  • Salary:Salary negotiable
  • Employment Type:Full Time, Permanent
  • Job Function:Laboratory  

Job Description

(Circa HKD55~70k per month)

 

The Client

 

Our client is a global pharmaceutical group that offers top-quality medicines for customers to enhance their well-being and quality of life. It is expanding its production capacity with a new facility. This job is based in Hong Kong, Asia.

 

Responsibilities

 

To set up a new QC laboratory

 

  • To lead a project team to set up the laboratory of a new pharmaceutical plant compliant with HOKLAS/GLP standards and resolve technical and administrative issues
  • To ensure that that equipment qualification/calibration, analytical method validation and GMP documentation are carried out as scheduled

 

To manage QC laboratory and services

 

  • To manage the initial operations of the QC laboratory in accordance with company objectives and priorities
  • To set up and implement quality systems and strategies
  • To collaborate effectively within the QC group and across different functional groups to deliver the QC department’s targets
  • To communicate with Government Bureau on GMP related issues

 

To lead and manage the QC team

 

  • To manage the departmental team and its resources
  • To coach and develop QC group members with highly professional standards
  • To make sure that quality risks are correctly assessed, identified and managed for all project management activities and product development procedures

 

Requirements

 

  • Bachelor degree or above in Pharmaceutical Sciences or a related Science discipline, preferably in Chemistry or Microbiology
  • 10 years’ experience minimum in pharmaceutical industry with a solid experience in laboratory management
  • Experience working in PIC/S, ISO, HOKLAS and other related quality management system
  • Conversant with GxP regulations, guidelines and quality standards, and strong working knowledge of ICH, PIC/S, GAMP5 and cGMP
  • Effective leadership, staff engagement and conflict resolution skills
  • Strong computer, documentation, communication and organizational skills

 

Application

 

If you would like to apply for this position or find out more, please apply ONLINE with CV in WORD format, stating your present and expected salaries and availability, or contact Mr. Ho at +852 6076 3139. Please kindly note that only shortlisted candidates will be notified.

 

Personal data collected will be used for recruitment purpose only.

 

Company Info

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