Advertised: 10-07-10 | Closing Date: 09-08-10

Austar is a leading company in the pharmaceutical industry. Austar's two core domains are Engineering and Equipment; providing professional solutions in Clean Room Systems and Liquid Process System as well as manufacturing and managing sales of equipment such as Purified Water Production System, Dry Heat Sterilizer. Austar also provide Sterile Product Filling Line products and services, and represent the leading Phamaceutical Equipment from Europe and US.
 
 
Austar has been keeping long-term business relationship with more than 30 foreign suppliers from Europe and America. Its products and service focus on high-end customers. In mainland China, there are more than 300 customers including large-sized pharmaceutical enterprises, scientific research institutions, as well as multinational pharmaceutical companies.
 
 

Validation Consultant
(China - - Shijiazhuang City - Hebei)

Responsibilities:

o Participating in sales promotion activities of validation consultancy projects and providing technical supports in validation consultancy
 
o Participating the execution of validation consultancy contracts and mainly responsible for the preparation of VMP, the Risk Assessment and the GMP Review, and the review of validation protocols and validation reports
o Providing internal training to validation engineers of Austar China to improve the level of the engineers
 

Requirements:

  • Candidate must possess at least a Bachelor's Degree, Post Graduate Diploma, Professional Degree, Engineering (Bioengineering/Biomedical), Engineering (Chemical), BioTechnology, Chemistry or equivalent.
  • At least 10 year(s) of working experience in the related field is required for this position.
  • Preferably Senior Executives specializing in Engineering - Chemical or equivalent.
  • Full-Time positions available.
  • Quite familiar with the VMP/Risk Assessment/GMP Review service for new pharmaceutical plant.
  • Quite familiar with the DQ/IQ/OQ/PQ service for HVAC system / Clean utilities / Process equipments.
  • Participated in a validation project which passed the cGMP compliance inspections of FDA (USA), EMEA (EU) and WHO.
  • Familiar with the production process of vaccine or with good experience of working in the aseptic dosage production manufacturer.
  • Familiar with FDA (USA), EMEA (EU) and WHO regulations and practice for the vaccine production or the aseptic dosage production.
  • Experience of doing validation jobs in the USA/EU Pharmaceutical manufacturing plant or engineering companies.
  • Required language(s): Preferably English or Chinese Speaking candidates required to service customers in China

Application Deadline: 10 August 2010
 
Number of Vacancies: 2


 



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