Beschreibung
Our client, a global pharmaceutical company, is looking for two experienced Qualification Engineers to support multiple ongoing projects on site.This is a fantastic, long term opportunity, working in a fast-paced environment.
Location: Eastern Germany
Start: As soon as possible
Duration: 12 months+
Responsibilities:
Carry out Qualification activities.
Write and execute IQ/OQ/PQ protocols for equipment such as blending, mixing, filling, dosing, packaging, HVAC, cleanroom.
Carry out Risk Assessment as well as design and deviation reviews.
Write, review and approve URS for equipment.
Support validation master plan.
Work alongside a group of process engineers.
Requirements:
Ideally degree educated (chemical/mechanical/process engineering or chemistry).
Strong experience working within the pharmaceutical industry, ideally with the above mentioned equipment.
Hands on experience of planning and executing qualification activities.
Strong GMP background.
Fluent German and English skills.