Job Description
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.
Si le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación.
We are looking for a Process Validation Specialist to support validation activities related to aseptic filling operations within a GMP-regulated pharmaceutical manufacturing environment.
Responsibilities include, but are not limited to:
- Support the planning and execution of process validation activities related to filling operations.
- Assist in the preparation and review of validation documentation , including protocols and reports.
Ready to Apply?
Submit your application today and join our talented team at PQE Group.
Submit ApplicationJob Details
- Location barcelona, kingdom of spain
- Job Type Full-time
- Category Manufacturing
- Posted Date June 05, 2026
- Application Deadline July 15, 2026