Quality Manager

Company Overview: Our client, established in 2019, is located in Bailly-Romainvilliers near Paris, France. The company provides premium-class cell culture products to national and international customers. These products are manufactured in a clean room facility and comply with the highest regulatory biopharmaceutical standards. Role Description: This is a full-time on-site role for a Quality Manager in Bailly-Romainvilliers. The Quality Assurance Specialist will be responsible for quality assurance, management, and auditing tasks to ensure compliance with international guidelines and internal procedures. Responsibilities: Development and implementation of the quality management system: Develop and implement procedures and processes related to the company’s quality management system. Ensure that quality policies and standards are clearly defined and communicated to all employees. Ensure that the quality management system complies with applicable regulations and standards. Product quality control: Establish quality criteria for the company’s products. Implement quality control procedures to ensure compliance with established standards. Conduct regular inspections and tests to verify the compliance of products or services with specifications. Management of quality problems: Identify and solve quality problems, whether internal or reported by customers. Conduct investigations on quality problems to determine the root causes and implement corrective actions. Put in place preventive actions to avoid the recurrence of quality problems. Training and awareness: Train employees in good quality practices and quality control procedures. Raise employees’ awareness of the importance of quality and their role in achieving the company’s objectives. Organize continuous training sessions to keep quality knowledge up to date. Collaboration with other services: Work closely with production, R&D, procurement and other departments to ensure quality throughout the process. Participate in meetings and cross-functional projects to solve quality problems and improve processes. Evaluation and continuous improvement: Conduct internal audits to evaluate the effectiveness of the quality management system and identify areas for improvement. Analyse performance data and quality indicators to identify trends and opportunities for improvement. Implement continuous improvement actions to strengthen the quality of products. Training and Knowledge Required: Bachelor’s degree +5 (Master or Engineer) in biotechnology, biology, chemistry, pharmacy or comparable training. 5 years of practical experience in the pharmaceutical industry including a minimum of 1 year management experience. Experience in internal audits and inspections is an asset but is not mandatory. Experience working in GMP or ISO 8 cleanrooms Familiarity with the ISO 9001 standard Ability to make decisions for yourself, set priorities and work autonomously. Fluent in English and French (written and spoken).