We are seeking a

Qualification/Validation Specialist (m/f/d)

for the Biotechnology/Pharmaceuticals sector (full-time/part-time) – fixed-term contract for 2 years – to start as soon as possible

. In this position, you will support the managers and employees of the manufacturing and qualification/validation departments with documentation and planning tasks. You will carry out your assigned tasks independently and be the primary contact person for all relevant interfaces within these projects. You can expect a diverse range of responsibilities – from planning and document creation at your desk to practical implementation at the production facilities.

Your responsibilities:

o Independent planning and execution of qualification projects in coordination with the technical supervisor and the responsible process owner

o Creation and processing of qualification documents in compliance with GMP-compliant documentation regulations

o Independent organization and management of assigned tasks

o Independent execution of routine and organizational tasks (e.g., document archiving)

o Processing of (sub-)projects in the area of ​​process and cleaning validation

Your qualifications / profile:

o Completed vocational training as a pharmaceutical technician, chemical technician, PTA, or similar, as well as Bachelor's degrees in a natural science field

o Ideally, several years of professional experience in a GMP-regulated work environment

o Experience in the independent planning and execution of qualification projects

• o Strong communication and teamwork skills