Qualification Expert

m/w/d, Aargau

We are looking for a candidate who is experienced in qualification of equipment and/or facilities within a GMP environment, preferably the pharmaceutical industry.

Your Responsibilities:

Responsible for planning and conducting qualification and validation activities
Creating and reviewing qualification and validation documents
Producing SOPs and providing support in the creation of manufacturing specifications
Responsible for maintaining the qualified and validated status of rooms, infrastructure and equipment
Ensuring compliance with internal and external regulatory requirements with regard to qualification and validation
Collaborating closely and communicating intensively with other departments
Providing assistance in the processing of deviations, changes and CAPAs

Your background:

Technical degree in a relevant field
Further training and hands-on experience in the area of GMP
3-5 years of experience in the qualification and validation of machines and processes, preferably in the pharmaceutical industry
Several years hands on work experience in qualification
Experience with Siemens COMOS, EVAL and VIVA

Apply now

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