Freelance / temporary employment for a project in Valais. Start date: asap. Reference number: 767909 / 1
Your responsibilities
* Holds all quality related responsibilities for daily qualification activities on technical facilities, equipment and systems.
* Supports the development, reviews and releases qualification documents.
* Assesses and approves change requests with regard to their relevance to the qualified state condition and ensures this supports and approves quality risk analysis.
* Ensures that deviations are appropriately investigated and addressed in deviation reports processed in deviation reports.
* QA activities follow legislation, authority and customer expectations.
* Informs the Group Manager QA Qualification about relevant developments and trends.
* Actively supports the formulation and further development of qualification strategies and continues to train accordingly.
* Supports internal audits in accordance with the internal audit plan, at customer audits and official inspections as QA representative.
Your profile
* Experience in biotechnology or pharmaceutical environment.
* Experience as QA Qualification.
* Knowledge on FAT / SAT / IQ / OQ / PQ.
* You are proactive, with good communication skills and are able to work in a multidisciplinary team towards a common goal.
* You are fluent in English (spoken and written).
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