ALTERNANT - CHARGE DE QUALITE DRUG PRODUCT

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 ensuring 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 employees 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

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