As part of PageGroup, Michael Page is a leading professional recruitment consultancy specialising in the recruitment of permanent, contract and temporary positions on behalf of the world's top employers. PageGroup operates through 155 offices in 35 countries worldwide. First established in London...
As part of PageGroup, Michael Page is a leading professional recruitment consultancy specialising in the recruitment of permanent, contract and temporary positions on behalf of the world's top employers. PageGroup operates through 155 offices in 35 countries worldwide. First established in London in 1976, we've been bringing jobseekers and employers together for more than 30 years. London listed, we opened our first Asian office in Hong Kong in 1994 and currently we have offices in all major business hubs across the APAC region, including Australia, Singapore, Tokyo, Malaysia, India, Taiwan, Shanghai, Beijing, Shenzhen, Guangzhou, Pudong and Suzhou.

So if you're looking to take your career to the next level, visit www.michaelpage.com.hk

Validation Supervisor - New GMP Plant

Job level Middle
Work exp No work experience
Education Associate Degree
Location
Within Hong Kong
Employment type Full Time
Industry Medical Services / Pharmaceutical / Hospitals
Job function Medical Services > Pharmaceutical
Quality Control / Quality Assurance > ISO, International Organization of Standardization
Manufacturing > Production Planning / Control
Published On 15/07/2019
ref. 4076359/001_19879

A Validation Supervisor in charge for the new GMP pharmaceutical manufacturing plant.

Client Details

Our client is a fast growing pharmaceutical manufacturer who expanding the production line rapidly. They have GMP manufacturing plants across Hong Kong and China. They are currently launching a new GMP plant and looking for an experienced validation supervisor.

Description

  • Handle and supervise the validation from engineering, manufacturing, transport/ installation, start up, process optimisation to routine production.
  • Responsible for process, equipment and facilities qualification like URS, DQ, FAT, SAT/IQ, QMS.
  • Liaise with different cross functional departments for Ad-hoc GMP validation related tasks.

Profile

  • Higher diploma or above in Chemical Engineering, Bio-medical Engineering or Qualification/ Validation, pharmaceutical/ manufacturing related disciplines.
  • 5 years + or Qualification/ Validation experience in pharmaceutical field.
  • Solid knowledge in GMP and pharmaceutical related regulatory will be preferable.
  • Good command of spoken and written English and Chinese.

Job Offer

  • 13 months Salary plus performance bonus
  • medical allowance
  • friendly management and casual company culture

To apply online please click the 'Apply' button below. For a confidential discussion about this role please contact Jeff Poon on +852 3412 4841