Validation engineer aseptic manufacturing

EngiFlex

  • Rosia, Siena
  • Tempo indeterminato
  • Full time
  • 1 mese fa
  • Candidati facilmente
Role and responsabilities:
  • Commissioning and qualification of new and existing equipment
  • Assuring appropriate risk management in the validation strategy
  • Writing URS of pharma equipment
  • Performing testing and validation activities (FAT and SAT)
  • Ensuring that adequate documentation is available for operations and QA
  • You will be working in cross-functional teams in a project or operational environment
Your background:
  • Experience in the pharmaceutical sector as validation or C&Q engineer
  • Experience in commissioning and qualification of equipment or processes such as formulation, filling, cleaning, sterilization
  • Candidate must speak fluent English. Italian is an asset. Dutch is not required.
  • The location of the project is NORTHERN ITALY with a good airplane connection to Brussels
Conditions:Full-time contract. (Freelance also possible)You will be part of a growing Belgian SME where initiative and personal development are encouraged. We will provide you with an enjoyable work environment with fun colleagues. Well work out a career plan with you, with attention and a budget for extra education/certification. You can count on an attractive salary, supplemented with extra-legal benefits, including a company car.

EngiFlex