Description
Randstad Life Sciences is seeking a Process Engineer specializing in Validation for an urgent consulting assignment with AstraZeneca in Snäckviken, Södertälje. The role supports qualification and validation documentation for process and production equipment, structures and archives GMP-compliant documentation, maintains quality and document management systems, coordinates workflows, and handles deviations and change requests. Candidates need GMP and pharmaceutical documentation experience, IQ/OQ/PQ knowledge, digital quality-system experience, strong administrative skills, and Swedish and English proficiency; the position requires on-site work three days per week.
