Beschreibung
A global pharmaceutical organisation is looking for experienced Qualification Engineers to support the start-up and GMP compliance of a new manufacturing facility.This is a fantastic long-term opportunity to work in Switzerland's thriving pharmaceutical industry.
Location: Basel area, Switzerland
Duration: 12 months +
Role and Responsibilities:
Qualification of new process equipment in a new production building for solid dose manufacturing
Reviewing and approving the user requirement specifications, technical specifications and commissioning documentation for new process equipment
Generating and executing DQ/IQ/OQ/PQ protocols
Writing user SOPs for new equipment
Ensuring that the qualification is completed in compliance with regulatory (GMP/FDA) and corporate guidelines
Requirements:
Degree educated in Chemical/Process/Mechanical Engineering, Pharmacy, Chemistry or similar
Experience working on the qualification or pharmaceutical process equipment
Technical knowledge of solid dose production equipment and processes (granulation, blending, dispensing, powder filling, tableting, coating)
Apply now for further details.