Expires soon SANOFI AVENTIS GROUPE

QUALITY PROJECT MANAGER HF

  • V.I.E.
  • Neu Isenburg (Regierungsbezirk Darmstadt)
  • IT development

Job description

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 in patients’ daily life, wherever they live and enable them to enjoy a healthier life.
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.
Therefore, only applications that are submitted in English will be considered.
At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.
We are looking for a candidate for a VIE mission of:
Quality Project Manager
- VIE Contract (W/M)
Responsibilities:
The position is placed within the GSA (Germany, Switzerland and Austria) spectrum. The VIE will provide support to the local Quality team in all areas of the activity, including:
- Support quality operations with focus on product quality, interaction with local authorities and production interfaces (internal and external) and with global quality functions (Paris)
- Close collaboration with other organization countries: Austria and Switzerland
- Managing third parties and providing support to quality agreement management
- Quality support with a focus on quality systems: documents, training, processes, deviations and CAPA (Corrective and Preventive Action)
- Leading and supporting quality projects
- Providing support to the Head of Quality Systems in all areas
- Coordinating of internal and external audits
- Ensuring compliance with Global Quality Policies and Standards and with local regulations
- Providing data analysis to identify areas for improvement
- Preparation and review of affiliate SOPs (Standard Operating Procedures)
Requirements:
- Master’s degree in Pharmacy or other life science relevant to the position
- Previous experience in: quality assurance, regulatory affairs, good practice or pharmacovigilance
- Previous experience in the pharmaceutical area would be an advantage
- Proficiency in MS Office package
- Fluent English and German
- Good project management and organizational skills
- Strong time management and prioritization skills
- Ability to work cooperatively with others across the organization to achieve shared objectives
- Strong customer focus: being dedicated to meeting the expectations and requirements of internal and external customers; getting first-hand customer information and using it for improvements in products and services; acting with customers in mind; establishing and maintaining effective relationships with customers as well as gaining their trust and respect
- Demonstrated ability to solve problems and urgent sense related with compliance with the quality requirements

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