Posizione: Associate

Tipo di lavoro: Full-time

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Contenuto del lavoro

For one of our clients active in the pharma industry, we are looking for a C&Q Engineer to manage challenging Commissioning & Qualification activities

Tasks

  • Act as C&Q Subject Matter Expert to provide guidance and to manage suppliers and all C&Q activities for the systems, from design to field execution and to summary report approval
  • Draft, coordinate review and approval of C&Q documents (QRA/DV/RTM/FAT/SAT/IOV/VSR)
  • Drive verification testing, protocol execution, walk-downs, verification of system drawings and troubleshoot as required
  • Conduct deviation investigation and resolution, take appropriate corrective actions as required
  • Responsible for the Planning, Tracking and Reporting of C&Q status and risks/issues for the selected systems
  • Review and accept turnover of equipment / system
  • Ensure Start-up of equipment/ system is completed in a safe and coordinated manner
  • Generate and review Change Controls related to C&Q
  • Facilitate the development of URS and Quality Risk Assessment for Equipment and Systems

Have you got what it takes?

  • Bachelor or Master’s degree in Engineering or in Life Sciences with relevant experience
  • Experience delivering Commissioning and Qualification for Pharmaceutical / Biotechnology projects
  • Understanding of a risk-based approach to C&Q

Benefits

  • Challenging projects based on your interests and skills
  • Personal follow-up and clear, transparent communication both before and after commencement of employment
  • Possibility to follow extra training
  • Inspiring network events and legendary after work drinks
  • Strong network of industry leading clients
  • Expertise within IT, Engineering and Life Sciences
  • A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees
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Scadenza: 10-01-2026

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