Contract: permanent
Location: Neuilly-sur-Seine (92)
About the job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as Global Inspection readiness lead within our Global Quality department, will be 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, and Suppliers for compliance with Sanofi / CHC Quality Policy / requirements and applicable regulations through audit and inspection support activities.
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At Sanofi Consumer Healthcare, we build trusted and loved brands that connect with hundreds of millions of consumers worldwide. Our mission is to enable better self-care for individuals and communities, while also contributing to a healthier planet. We strive to act as a force for good by integrating sustainability along our business and employees' mission and operate responsibly from both a social and environmental point of view. To achieve this, we need people who can shape the future of our business and help us on our journey to becoming the best fast-moving consumer healthcare company in and for the world.
Main responsibilities
- Support sites and other entities (affiliates) across the world to ensure inspection readiness and inspection follow up as necessary.
- Manage a group of auditors based in Budapest (European audits in different locations)
- Provide expertise on worldwide GMP requirements.
- Analyze new GXP requirements and communicate them to the impacted entities.
- Organize global communications / meetings with the Quality network sharing the outcome of inspections to ensure that the findings raised by the different authorities are considered by all concerned entities.
- Ensure the follow-up of inspection key indicators.
- Perform audits as a qualified auditor
- Support the training & qualification of auditors.
About you
- Pharmacist or advanced degree (e.g., Master, PhD or equivalent) in life sciences or related fields
- 10+ years working experience in Quality management and auditing in Pharmaceutical Industry in multinational environment or across different countries and markets
- Excellent 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 10 years in a GMP/GDP environment.
- Organization and communication skills, networking capability, leadership and assertiveness skills.
- English spoken and written compulsory. French is a strong asset.
Why choose us?
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Pursue Progress. Discover Extraordinary.
Progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let's pursue progress. And let's discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com