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Quality Control Specialist - Portugal (m/f)


  • Raw and Packaging material Team leader
  • LIMS and SAGE Key user: database management (information on equipment's, consumables and raw material, packaging material, drug products and stability specifications updated as needed)
  • Product sampling and testing in the scope of routine testing
  • Prepare and review documentation (analytical methods, reports and others), statistical data analysis, according to the implemented systems, for internal use and for regulatory purposes
  • Establish and maintain strong partnership to internal and external customers and stakeholders
  • This position is will be responsible for direct communication to inspectors and auditors
  • Responsible for OOS investigation and CAPA related activities
  • Assure the separation of waste according to the internal environmental system
  • Compliance with technical, organizational and staff safety measures, including the emergency procedures
  • Ensure adequate confidentiality to documents, data as well as all company related knowledge and trade secrets
  • Ensure compliance support to relevant applicable regulations and standards
  • Assure accurate and efficient preparation / revision of data and documentation within agreed timeframes
  • Advance degree in Pharmaceutical Sciences, Chemistry or related technical field (Master or PhD)
  • Strong understanding of GMP requirements for pharma industry with quality control/compliance background
  • Excellent knowledge of different physical and physicochemical methods of analysis (such as HPLC, NIR, RAMAN, FTIR, Titrations)
  • Good working knowledge of IT Systems such as, SAGE, LIMS, LMS TRACKWISE, Minitab and Empower
  • Proficient in English
  • 3-5 years' experience in Pharma industry
  • Knowledge of French and German


» Job description


Employer:
Vifor Pharma
Location:
Amadora [P]


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