As the Site Quality Control Director, you are responsible for the overall management of the QC department and leadership of the Microbiology/Sterility and Chemistry labs. It is also critical that a change management and continuous improvement strategy is implemented across the QC department.
It is also important there is a maintenance and improvement of the QC Quality Systems to ensure quality control and documentation in line with global Good Manufacturing Practices, ISO and ICH. You will also be responsible for approving contracts with external clients for the QC area, review and approve regulatory documents for formulation and testing, and lead critical project initiatives.
Extensive knowledge of the pharmaceutical industry, Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and Quality Management Systems.
Experience in working in a highly-matrix organisation
Success in implementing change-management methodologies and continuous improvement to a department in a manufacturing facility
Leadership experience with control of team budget
University degree in Science
Excellent command of the English language, written and oral
Competitive base salary, reflective of the local market
End of year Key Performance Index bonus
Competitive health insurance and company pension