Reporting to the Group Quality Manager (who is also our Group Data Protection Officer), the Regulatory & Quality Engineer ensures that the company's quality policy is implemented and respected, and plays a pivotal role in matters relating to the Quality Management System.
Operating in an environment with high regulatory requirements, they contribute to the efficiency of the company's processes while ensuring compliance with applicable standards throughout the company’s subsidiaries.
Hybrid or Home-based possible.
Conduct regular internal audits to identify areas for improvement and ensure adherence to quality standards.
Contribute to the creation, maintenance, and organisation of quality-related documentation, including SOPs, work instructions, quality manuals, records and training material.
Establish key performance indicators (KPIs) and metrics to measure and monitor quality performance throughout the organisation.
Collaborate with cross-functional teams to resolve quality-related issues and implement corrective/preventive actions in a timely manner.
Active Contribution to Quality Culture and Awareness
Train and educate staff on quality procedures and best practices.
Champion a culture of quality throughout the organisation, promoting awareness, accountability, and a relentless focus on customer satisfaction.
Regulatory Monitoring / Compliance
2 - 3 years’ experience in the role out of Quality policies.
~ Knowledge of Quality Management Systems (QMS).
~ Fluent in English (ideally with business French).
Data Protection Officer certification.
Knowledge of regulatory requirements specific to the pharmaceutical industry (e.g., Experience with Agile or Scrum Methodologies.
Proficiency in Electronic Document Management Systems (EDMS) and other quality management software.