Project Engineer Qualification

at  Exyte GmbH

Stuttgart, Baden-Württemberg, Germany -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate03 Oct, 2024Not Specified03 Jul, 2024N/ACommunication Skills,Iso,Validation,Data Integrity,English,Gmp,Biotechnology,Medical DevicesNoNo
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Description:

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.

Responsibilities:

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


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Electrical/Electronic Manufacturing

Engineering Design / R&D

Electrical

Graduate

Proficient

1

Stuttgart, Germany