4 beste Stellen als cqv engineer in basel, bs – aktuell auf Personalsuche

Shape innovative projects in the pharmaceutical industry and take on responsibility in exciting qualification and validation projects within a dynamic environment at Exyte.

Explore your tasks and responsibilities

Preparation of qualification and validation plans
Preparation and review of specifications, risk analyses, design documents, and project processes
Planning and execution of DQ, IQ, OQ, and PQ for production equipment
Preparation of qualification reports
Review of supplier documentation and coordination of supplier activities
GMP-compliant documentation of executed work
Handling of changes and deviations (Change Control & Deviations)
Preparation of Standard Operating Procedures (SOPs)
Maintenance and archiving of documentation
Ensuring training standards of project team members
Leading a project team (up to 3 people)
Project management of smaller projects (time, budget, resources)
Supporting and mentoring junior engineers
Independent execution of work packages (WPs) and smaller projects

Show your expertise

Degree in engineering, natural sciences, or a pharmaceutical-related field
Willingness to travel within Switzerland
Strong knowledge of GMP regulations and common industry standards
High level of quality awareness and attention to detail in documentation
Several years of professional experience in the pharmaceutical industry
Very good German and good English skills (corporate language)

Contact:

You want to be part of the Exyte team? We look forward to receiving your application!
For further questions and information, please do not hesitate to contact Ilayda Öztürk via E-Mail at [email protected].

Please note that we only consider applications submitted through our application portal. Applications sent via email will not be considered due to data protection regulations.

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