About the job

At Sanofi Consumer Healthcare , we have one shared mission – we work passionately, every day, to ‘serve healthier, fuller lives’ now and for the generations to come. In order to do so, 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. Everything we do is centered around people’s interests – our consumers, our customers, healthcare professionals, and our employees – across the world. We are building loved brands that serve our consumers worldwide, through our key platforms: Allergy, Physical & Mental Wellness, Pain, Digestive Wellness and Cough, Cold & Flu. We aspire to become the best Fast Moving Consumer Health (FMCH) company In & For the world and we aim to build a work environment where people can thrive, grow, enjoy and be at their best.

Our Team:

EM CHC Quality Assurance Drug department main goals is e nsuring an appropriate Quality oversight of Contract Manufacturing Organizations (CMOs) and sub-contractors acting for EM CHC. To guarantees compliance with GMP and corporate requirements for all regulated activities. The team is a combination between Gentilly and Frankfurt employee s which creates an international work environment .

Main responsibilities:

  • Creation and maintenance of the records:

  • Maintenance of attribute fields, APIs, excipients, primary packaging materials for assigned products

  • QSMP statements for assigned products

  • Maintenance of quality assurance agreements / annexes and other relevant documents

  • Creation of queries from databases (e.g. CONNECT) in cooperation with team leader, Quality/Regulatory Manager

  • Maintenance of product list for assigned products

  • Creator or document manager in CMS CONNECT like e.g. archiving of PQRs, GAP assessments

  • Support of master data check for new GMIDs

  • Key user, super user etc. for assigned computerized systems and SME for assigned processes

  • Support of inspections

About you

  • Experience : You have experience in Pharmaceutical Quality department or in pharmaceutical industrial environment is appreciable.

  • Soft skills : You are a team player, eager to develop your skills and learn, and you are proactive.

  • Technical skills : - Quality documentation writing skills- Knowledge of pharmaceutical quality management. Experience in Quality Management System (project or routine mode) would be a plus

  • Languages : Fluent in English & French

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But 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. So, let’s be those people.

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 (https://www.youtube.com/watch?v=SkpDBZ-CJKw&t=67s) and check out our Diversity Equity and Inclusion actions at sanofi.com (https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness) !