Quality Process Owner

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Teoxane SA

Beschreibung:	Quality Process Owner
Stadt:	Genève, Schweiz
Firma:	Teoxane SA - Firma bewerten
Datum:	2026-02-11
Beschäftigung:	bis 100%
Salär:	zu verhandeln CHF - 40 Std/Woche
Arbeitsort:	Schweiz

BEWERBEN

Tasks: Quality Process Owner

Quality Process OwnerYou can find all of our job offers by clicking here: A major independent player in aesthetic medicine and dermo-cosmetics, Teoxane is dedicated to men and women who want to feel their best over time, pushing the boundaries of aesthetic medicine and challenging the market. Thus, we invent safe, proven solutions inspired by the thousands of cases clinicians encounter each week. Our expertise in hyaluronic acid allows us to offer high-performance filler products and dermo-cosmetics in more than 90 countries worldwide, making us the 3rd largest global player in hyaluronic acid-based fillers. As part of our strong growth, we are recruiting for:Quality Process OwnerA position focused on Change Control and Risk Analysis Management, including risk management files, its updates including annual reviews, contact with regulatory submissions, supervision of working groups, and updates of files (Change Control, Non-conformities, and CAPA ). This role requires a minimum of 6 years of experience.A position focused on Integrity and Internal Audit, involving support for the annual internal audit plan, internal auditors, and steering action plans for internal audits. This role requires a minimum of 8 years of experience ideally.Main activities for both roles:- Be responsible for the processes of the X system ensuring: - Compliance with applicable regulations and standards, - Support for cross-functional teams, - Definition and analysis of processes as well as the implementation of tracking tools for process efficiency, - Continuous improvement,- Contribute to the proper execution of all quality system processes,- Conduct audits on quality processes in collaboration with the quality team,- Contribute to the monitoring and execution of audits.Profile:- Experience in a quality system role with 6-8 years of experience, ideally in the medical device sector,- Mastery of quality references ISO, MDSAP and 21 CFR part 820,- Minimum B2 English proficiency,- Knowledge of VEEVA or eSMQ is a plus. jida994a2faen jit0207aen jpiy26aen