PROJECT MANAGER COUNTRY QUALITY HF

Job description

PLEASE NOTE that only applications submitted in English can be considered by our non-French speaking partners at Sanofi worldwide. Therefore, it is strongly recommended that you post your resume in English.
Program SaVIE (VIE of Sanofi) is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
Enterprise:
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.
Sanofi is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY).
For more information, please visit http://www.sanofi.com
Mission:
New challenges in the area of quality assurance concerning company reorganisation and integration of new product types such as vaccines into the quality management of the commercial organisation.
To maintain full operational capacity and full compliance with all national and corporate regulations during transition, increased need to cooperate along the interfaces to global quality functions (Global Quality Commercial Operations and External Manufacturing in Paris, Global External Manufacturing Gx in Prague), ongoing growth of the Generic business (Zentiva)
Support of the German Country Quality Operations team in the following acitvities:
- Quality of Producs: focus on product quality for marketed products, quality issues and product technical complaints,
interaction with local authorities and production interfaces (internal and external) and with global quality functions (Paris, Prague), inspection readiness, GMP documentation
- Work closely together with the other Multicountry Organisation Countries Austria and Switzerland, manage PQRs, GMP documentation, support legal batch release process, Quality agreement management, support Qualified Person and wholesaling representative in all areas
- Quality systems (SOPs, training and processes)
- Project management of a quality project in order to take over full responsibility of a Quality Center of Excellence
either for Quality agreements or GMP documentation
In order to interact with all departments, intermediate German knowledge is required .
Profile:
Graduated in Pharmacy
Previous work as a student in the pharmaceutical area
Professional skills/attitude and behaviour requested:
Keen and curious to learn and acquire new knowledge, committed, skilled in the use of computers, team player, having the patient's needs in mind, quality mindset (accurate, thourough workstile), preseverance to work on topics that stretch over a longer time
FULL PROFICIENCY IN ENGLISH IS MANDATORY
GOOD PROFICIENCY IN GERMAN IS REQUIRED (MINIMUM B1 LEVEL)