Job Description
Our people are our success. As one of us, you will contribute to engineering excellence for the high-tech markets of the future, including semiconductors, batteries, pharmaceuticals, biotechnology, and data centers. At Exyte, you will be part of a global community of challenge seekers who are ambitious and passionate about innovation. Together, we will build on our company's long history and keep on leading the way to a better world.
Exyte is a global leader in design, engineering and delivery of facilities for high-tech industries - serving people and planet by energy saving & more sustainable engineering.
As (Junior) Project Engineer (m/f/d) Pharma / Food with focus on Qualification / Validation, you work in the Bio Life Sciences sector at Exyte Central Europe and report to the Group Lead Qualification & Validation.
You are going to be assigned to our regional office in Nuremberg and with our clients on-site to qualify the respective equipment and facilities.
In a team of highly qualified and experienced qualification & validation engineers you will be covering exiting pharma projects. Mobile working is also a possibility, depending on the project.
Explore your tasks and responsibilities
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Responsible handling of project-specific qualification and validation activities according to current GMP regulations for HVAC-, Cleanroom- & Clean Media-Systems
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Preparation and review of qualification & validation documents (specifications, risk analysis, plans and reports)
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Preparation of test protocols for different qualification stages (DQ, IQ, OQ, PQ) and being responsible for their execution
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Responsible for supplier coordination and review of supplier documentation (FAT/ SAT, technical documents)
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Responsible for the communication between qualification, customer/user, technical engineers, automation, QA, and suppliers as well as reporting to the CQV manager /project management
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During the implementation phase, you are on-site to coordinate and conduct the qualification independently. You are able to work under time pressure and to successfully drive the project forward
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Completed studies in the field of biotechnology, pharmaceutical or process engineering, medical devices or a related field of study
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Relevant technical knowledge of current regulations in qualification and validation (GMP, ISO, 21 CFR, Annex 15, data integrity, ISO14644)
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You have gained a first insight into qualification/validation during your first job or during an internship (ideally in the life sciences industry)
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Fluent written and oral communication skills in English. Good German skills are required
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Proactive and independent working style as well as a high level of quality awareness, efficiency and accuracy
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Your start at Exyte: You will take part in a two-day onboarding event with new colleagues
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Attractive location: Our location in Stuttgart offers spacious workplaces with height-adjustable desks and two monitors
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Buddy system: Several weeks of close familiarisation with your colleagues in the team
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Work-life balance: Possibility of mobile working depending on project requirements and after consultation with your supervisor
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Jobbike: Leasing of a company bike through salary conversion and financial support by Exyte
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Keep fit: Exyte subsidises your fitness contract through Qualitrain at over 5,000 locations in Germany