Engineer Qualification cleanroom technology (m/f/d)
at Exyte GmbH
Nürnberg, Bayern, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 03 Oct, 2024 | Not Specified | 03 Jul, 2024 | N/A | Iso,Biotechnology,Gmp,English,Data Integrity,Validation,Communication Skills,Medical Devices | No | No |
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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
Other
Graduate
Proficient
1
Nürnberg, Germany