Junior Project Engineer Qualification / Validation (m/f/d)

☞ Exyte

Visualizza: 142

Giorno di aggiornamento: 22-10-2024

Località: Penzberg Bavaria

Categoria: Alta tecnologia Meccanico / Tecnico Elettrico / Elettronico IT - Software

Industria: Civil Engineering

Posizione: Entry level

Tipo di lavoro: Full-time

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Contenuto del lavoro

Your vision is ambitious. Just like ours.

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.

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 Qualification / Validation (m/f/d) , you work in the Bio Life Sciences sector at Exyte Central Europe and report to the Group Lead Qualification & Validation. You are going to work in our regional office in Penzberg 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 projects mainly in the south of Germany and in Austria. 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
  • 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 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)
  • 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 German, since the documentation language is German. Good English skills are required
  • Proactive and independent working style as well as a high level of quality awareness, efficiency and accuracy
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Scadenza: 06-12-2024

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