CQV ENGINEER* 80 – 100%

Your tasks

• Contact point for qualification questions
• Project management of CQV projects
• Sub-project management in larger projects
• Creation of templates for qualification-relevant documents such as FS, DS, DQ, FAT, IQ, SAT, OQ
• Supporting the project manager in creating qualification-relevant documents
• Supporting the project managers in document management with the customer
• Assisting the project manager with validation questions
• Keeping knowledge regarding regulatory requirements, GAMP, FDA, Swissmedic, etc. up to date
• Qualifications at customer sites on-site

Your profile

• Completed HF/FH training, preferably in process engineering, pharmaceutical environment, or several years of experience as a qualification engineer*
• Basic technical knowledge with strong imagination
• Experience in a GxP-regulated environment is an advantage
• Adept in handling organizational tasks and IT and PC systems
• Customer-oriented and entrepreneurial thinking
• Native German or French with good knowledge of the other language and the English language

Good reasons for your future with us

• Varied challenges await you in a collegial environment
• You will work on a project basis in multilingual and international teams and with people from all generations
• We value your development, whether on-the-job, with targeted training courses, or during Lunch & Learn
• Flexible working hours, part-time positions, and the possibility of home office for a balanced work-life balance
• Up to two weeks of additional vacation upon request – individually possible
• Our pension fund for your retirement provision – JAG offers above-average benefits
• You are a doer; flat hierarchies and simple structures give you a lot of freedom with us

Work location: 2555 Brügg

For further information, our HR team is at your disposal:

Lia Bachmann or Maitê Sacristão

Have we sparked your interest? We look forward to your application.

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