Project Engineer Cleanroom Qualification (m/w/d)

Your vision is ambitious. Just like with us. Our employees are our success. As one of us, you contribute to the technical excellence for the high-tech markets of the future, including semiconductors, batteries, pharmaceuticals, biotechnology and data centers. At Exyte you will become part of a global community of challenge seekers who are ambitious and passionate about innovation. Together we will build on the long history of our company and continue to point the way to a better world. Discover an exciting role Exyte is a global leader in the design, engineering and supply of equipment for the high-tech industry - serving people and the planet through more energy-saving and sustainable technology. As (Junior) Projektingenieur (m/w/d) Pharma / Food with focus on qualification / validation, you work in the Bio Life Sciences department at Exyte Central Europe and report to the Group Lead Qualification & Validation. They are used at our regional office in Nuremberg and at our local customers to qualify the respective equipment and equipment. In a team of highly qualified and experienced qualification and validation engineers, you will support exciting pharmaceutical projects. Depending on the project, mobile work is also possible.

Responsible implementation of project-specific qualification and validation activities according to the current GMP guidelines for HVAC, clean room & clean media systems Creation and verification of qualification and validation documents (specifications, risk analyses, plans and reports) Preparation of test protocols for different levels of qualification (DQ, IQ, OQ, PQ) and responsibility for their implementation Responsible for supplier coordination and verification of supplier documents (FAT/SAT, technical documents) Responsible for the communication between qualification, customer/user, technicians, automation, QA and suppliers as well as reporting to the CQV manager/project management During the implementation phase you are on site and coordinate and perform the qualification independently. You are able to work under time pressure and successfully advance the project

Complete studies in the fields of biotechnology, pharmaceuticals, process engineering, medical devices or related fields Including technical knowledge of the current requirements in the field of qualification and validation (GMP, ISO, 21 CFR, Annex 15, Data integrity, ISO14644) In your first job or during an internship (ideally in the life sciences industry), you gained a first insight into the qualification/validation Flowing written and oral communication skills in English. Good German knowledge required Proactive and independent functioning as well as a high degree of quality awareness, efficiency and accuracy

Your start at Exyte: Join a two-day onboarding event with new colleagues Attractive location: Our location in Stuttgart knows generous jobs with height-adjustable desks on Buddy system: Multi-week tight working phase with your colleagues in the team Work-life balance: There is the possibility to switch to mobile work again and again Food: Free coffee specialities and water dispensers are available on each floor Keep fit: Exyte grants your fitness contract via Egymp Wellpass at over 5,000 locations in Germany JOBV1_EN