La tua visione è ambiziosa, proprio come la nostra.

Le nostre persone sono il nostro successo. Come uno di noi, contribuirai all'eccellenza ingegneristica per i mercati high-tech del futuro, inclusi semiconduttori, batterie, farmaceutica, biotecnologia e data center. In Exyte, sarai parte di una comunità globale di cercatori di sfide, ambiziosi e appassionati di innovazione. Insieme, costruiremo sulla lunga storia della nostra azienda e continueremo a guidare la strada verso un mondo migliore.

Discover your exciting role

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

• Responsible handling of project-specific qualification and validation activities according to current GMP regulations for HVAC-, Cleanroom- & Clean Media-Systems
• Preparation and review of qualification & validation documents (specifications, risk analysis, plans and reports)
• Preparation of test protocols for different qualification stages (DQ, IQ, OQ, PQ) and being responsible for their execution
• Responsible for supplier coordination and review of supplier documentation (FAT/ SAT, technical documents)
• Responsible for the communication between qualification, customer/user, technical engineers, automation, QA, and suppliers as well as reporting to the CQV manager /project management
• 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

Show your expertise

• Completed studies in the field of biotechnology, pharmaceutical  or process engineering, medical devices or a related field of study
• Relevant technical knowledge of current regulations in qualification and validation (GMP, ISO, 21 CFR, Annex 15, data integrity, ISO14644)
• You have gained a first insight into qualification/validation during your first job or during an internship (ideally in the life sciences industry)
• Fluent written and oral communication skills in English. Good German skills are required
• Proactive and independent working style as well as a high level of quality awareness, efficiency and accuracy

What we offer you

• Your start at Exyte: Take part in a two-day onboarding event with new colleagues
• Attractive location: Our location in Stuttgart features spacious workstations with height-adjustable desks
• Buddy-System: Several weeks of close familiarisation with your colleagues in the team
• Work-life balance: There is always the possibility of switching to mobile working
• Catering: Free coffee specialities as well as water dispensers are accessible on every floor
• Keep fit: Exyte subsidises your fitness contract through Egym Wellpass at over 5,000 locations in Germany

CONTATTI:

Exyte è un datore di lavoro che offre pari opportunità di impiego ed è impegnato nell'offrire pari opportunità e trattamento. Pertanto, Exyte Group fornisce pari opportunità di impiego a tutti i candidati qualificati, indipendentemente dall'origine, genere, orientamento sessuale, identità di genere, razza, colore, religione, stato di veterano protetto, disabilità o informazioni genetiche.