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
Qualifications:
* Technical degree in a relevant field
* Further training and hands-on experience in the area of GMP
* Multiple years of experience in the qualification and validation of machines and processes, preferably in the pharmaceutical industry
* Hands-on work experience in qualification
* Experience with Siemens COMOS, EVAL, and VEEVA is an asset
* Fluency in German spoken and written needed, English fluency written and reading comprehension
* Very independent and structured way of working with a self-image of self and to continuously improve the processes
* High degree of initiative, flexibility, and quick comprehension skills
* Enthusiasm for working together in self-organized teams and for your own areas of responsibility with a focus on the big picture
Contract Details:
* Unlimited project contract
* Fascinating, innovative environment in an international atmosphere
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