CQV ENGINEER*IN 80 – 100%

Your tasks

• Point of contact for qualification issues
• 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
• Assisting project managers with document management with the client
• Mentoring the project manager on validation issues
• Keeping knowledge regarding regulatory requirements, GAMP, FDA, Swissmedic, etc. up to date
• On-site customer qualifications

Your profile

• Completed vocational training (HF/FH) preferably in process engineering, pharmaceutical environment, or several years of experience as a Qualification Engineer*in
• Technical basic knowledge with strong imagination
• Experience in a GxP-regulated environment is an advantage
• Proficient in handling organizational tasks and IT and PC systems
• Customer-oriented and entrepreneurial thinking
• Native German or French speaker with good knowledge of the other language and English

Good reasons for your future with us

• Varied challenges await you in a collegial environment
• On a project basis, you will work in multilingual and international teams and with people from all generations
• We value your development, whether it's on-the-job, with targeted training courses, or at 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

Workplace: 2555 Brügg

For further information, our HR team will be happy to assist you:

Lia Bachmann or Maitê Sacristão

Have we piqued your interest? We look forward to receiving your application.