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Global Audit Coordination Lead - all genders

塞纳河畔纳伊, 法国 Permanent Posted on   Dec. 23, 2024 Closing on   Mar. 28, 2025
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The Opella HealthcareGlobal Audit Coordination Leadis a member of the CHC Audits and Inspections team within CHC Global Quality.

The mission of our team is to define the CHC Global Quality Audit policy and to coordinate its implementation across the business and to provide an accurate, independent assessment of CHC sites, Development Centres, country offices, CDMOs, Pharmacovigilance and Suppliers for compliance with Sanofi CHC Quality Policy / requirements and applicable regulations through audit and inspection support activities.

Main responsibilities:

  • Defines in cooperation with the Global CHC Audits and Inspection team, the CHC annual quality audit plan. Monitorsthe audit schedule and adaptsthe plan as necessary to support Quality / Business needs throughout the year.
  • Supports quality audit process implementation
  • Supports the qualification of auditors
  • Interacts regularly with manufacturing sites, commercial offices, and Third Party Management teams
  • Is a qualified auditor performing audits (periodic professional trips are expected in this role).
  • Provides expertise and support and enhances good practices for process simplification and improvement.
  • Ensures the accuracy of the database for CHC auditsand supports follow-up of audit observations and corrective actions
  • Consolidates key indicators for quality audit and performance statusand prepares summaries and presentations for senior leadership
  • Supports the evolution of the tools/systems related to the audits & inspections and act of Business Process Owner for some processes.

About you

  • Experience:5-10 yearsworking experience in Quality management in Pharmaceutical Industry and/or distribution.
  • Technical skills:
    • Good knowledge of GXP regulations and pharmaceuticals standards for a wide range of products (CHC Drug Products, Neutraceutical, Cosmetics, Medical Devices)
    • Be a qualified auditor, minimum experience of 5 years in a GMP/GDP environment.
    • Good knowledge in technical environment as of use of eQMS, databases, extraction models, KPI management
  • Soft skills:Organization,communication and presentation skills, networking capability, leadership and assertiveness skills.
  • Education:Pharmacist or Life Sciences Graduate (e.g., Bachelor,Master, PhD or equivalent)
  • Languages: English / French spoken and written compulsory.

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进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。

在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。

观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!

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