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Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane strength is to offer a global patient care. Using its products, practitioners can fill a ...
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We are looking for an CSV Engineer to manage and validate computerized systems within our company. · ...
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We are looking for a CSV Engineer to manage and validate computerized systems within our company.At Teoxane Laboratories we have been established in Geneva since 2003, ...
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Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. · Ensure validated status and regulatory compliance of all computerized systems within scope thr ...
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Job Role: Global compliance lead – Digital Factory Program (DFP) · Global organization : Location : TBD - Switzerland · Experience: 10+ years · Duration : Long-term · Role Summary: · Company has introduced the digitalization program – Digital Factory Program (DFP) with the aim ...
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CSV Engineer - Geneva - Teoxane SA
Beschreibung
CSV EngineerYou can find all of our job offers by clicking here: /.Teoxane Laboratories were established in Geneva, Switzerland, inThey are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics.
Using its products, practitioners can fill all kinds of wrinkles, from the finest to the deepest, to restore youthful volume to the face, and to treat the neck and décolleté, with natural results.
The strength of Teoxane is also its human size and independence. Teoxane has total freedom of thought, action and innovation which makes the company unique.In the frame of the growth of our business, we are looking for an:
CSV EngineerMain activitiesManage and validate the computerized systems (CS) within the company.
Execute the validation of computerized systems and support the activities of the team under supervision.
Implement continuous improvement in the management of CSV activities.
Write and update instructions, procedures, and documentation necessary to control the CS.Develop IQ/OQ/PQ protocol and test sheets for software validation.
Serve as a reference for system validation during internal and external audits.Take charge of any other specific mission that could be assigned by management.
Report any risk situation to your manager or colleagues without delay.
Your profileUniversity degree in Engineering, Computer Science, or related field.
Minimum 2 to 5 years of experience in a similar position in the Pharma or MD industry.
Good experience in commissioning and system qualification.
Strong organizational, communication, and interpersonal skills.
Pedagogue, communication skills and good writing skills.
Dynamic and positive attitude, with the ability to thrive in a resource-constrained environment.
Effective problem-solving skills, especially in complex scenarios.
Fluent in French and English. jidf7b44fba jit0310a jiy26a
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