78 days ago on srconseils.ch

Document Quality Systems Manager

Cabinet SR Conseils SA

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Document Quality Systems Manager

Document Quality Systems Manager

Posted by  Fabrice

Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people at Sanofi are dedicated to make a difference on patients’ daily life, wherever they live and enable them to enjoy a healthier life. We are looking for a:

Documents Quality Systems Manager, in Vitry-sur-Seine (France)

Your Challenge:

As part of the QA Department, you are reporting to the Quality Systems Head. The main challenge for you is to ensure the design, the implementation and the Management of Quality Systems aligned with the overall Quality Systems Strategy. Basically, the Document Quality Systems Manager provides operational support to Managers and Teams by constantly collaborating with them.

Your main responsibilities as Document Quality Systems Manager are:

To ensure a proper design and a fast implementation of the Quality DocumentationSystems (QDS) Process

To be a driver and the reference in good documentation practices on site

To identify and suggest long-term improvements opportunities related to any quality system

To assist all Managers and Key users in QDS activities

To ensure constant quality system readiness through adequate preparation and training for inspections and audits

To actively participate as support team to the Inspection Readiness Program

Your Profile:

Academic training in Sciences, Quality or Management (Master Degree / Pharmaceutical Degree).Strong required experience (mini 5 years) in pharmaceutical industrial environment with direct accountabilities on Document Management Systems.Solid and recognized experience (mini 3 years) in a transversal role in a GMP environment.Good knowledge in Quality Documentation Process, Geode+ tool, MS Office. Very high level in both French and English.Strong team spirit, good communication skills, open mind, good leadership capabilities.

Excellent opportunity! Total confidentiality guaranteed

Thank you to send your updated CV to Fabrice Cattant