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Hovione is an international manufacturer of active pharmaceutical ingredient, inspected by the USA Health Authority and an ISO9001;ISO14001 and OHSAS18001 certified Company, following cGMP’s guidelines.

For our plant in Taipa we have now the following full time permanent jobs:

Quality Control Technical Coordinator

The Quality Control Technical Coordinator will be responsible to coordinate the assigned product/project specific analytical tasks and liaise between the analytical teams with other analytical sites. Ensure that the deliverables of each product/project are dealt in the QC laboratory within the timeframes defined, with quality and according to cGMP. It will also coordinate the QC staff in such a way as to guarantee the fulfillment of the Area objectives in accordance to all applicable regulations, and assist to promote a culture of demanding and continuous improvement standards in the Area.

Main responsibilities:

  • Assure the fulfillment of all cGMP requirements of the product/projects as well as the Safety, Environmental and Health Regulations;
  • Ensure the fulfillments of the release of raw materials, In-Process samples, intermediates, environmental testing samples, stability samples, cleaning verification and other miscellaneous samples sent for QC analysis;
  • Propose and coordinate the human, technical resources and the materials of the products/projects are in order to ensure the analyses performance;
  • Assure training of all Human Resources in such a way to guarantee the best support to the product/projects;
  • Guarantee qualification, calibration and good functioning of the instruments in the Area;
  • Comply and ensure compliance with the applicable cGMP and ISO standards;
  • Propose new methodologies and/or alternatives for the analytical tests of the products/projects, finding the right balance between analytical costs, client’s needs and regulations;
  • Assure that the instruments available are used in a productive and proper way and are maintained accordingly;
  • Meet the KPIs defined for the Area.


  • University degree in Chemistry/Chemical Engineering or equivalent;
  • Knowledge of analytical theory and experience of analytical practice;
  • Knowledge of Good Manufacture Practices and ISO standards;
  • Working experience in Quality Control Laboratory under cGMP;
  • Fluent in both written, spoken English and Chinese;
  • Familiar with MS-Office in English and Chinese;  
  • Good coordination and communication skills.


We offer:

  • Global career development;
  • Integration into a dynamic technical team of an International Company;
  • Promotion and high levels of responsibility;
  • Attractive remuneration, fringe benefits includes bonus, canteen, transportation and medical scheme.

Se deseja candidatar-se, selecione a opção Efetuar Candidatura Agora. Não aceitamos candidaturas de outras formas.