Akkodis, is a global leader in the engineering and RD market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis offers broad industry experience, and strong know-how in key technology sectors such as mobility, software technology services, robotics, testing, simulations, data security, AI data analytics. The combined IT and engineering expertise brings a unique end-to-end solution offering, with four service lines – Consulting, Solutions, Talents and Academy – to support clients in rethinking their product development and business processes, improve productivity, minimize time to market and shape a smarter and more sustainable tomorrow.Akkodis is part of the Adecco Group. Our Webstite : www.akkodis.comNote: the function described below is a permanent placement opportunity.Main tasks:To organise, manage, optimise and monitor the activities of 5 production lines (3 gels, 2 packaging) in compliance with :- Pharmaceutical regulations (GMP)- Quality, Safety, Health and Environment (QHSE) requirements- Costs and deadlinesLeading and supervising a production team as part of a continuous improvement process.Key responsibilities :1. Operations planning- Drawing up the short-term production plan- Issue production orders (PO)- Ensure availability of materials and equipment2. Production monitoring- Guarantee compliance with the schedule- Manage production contingencies (early/late)- Actively participate in production meetings- Coordinate technical and external interventions3. Continuous improvement- Leading continuous improvement initiatives (Lean, Kaizen, etc.)- Analyse the root causes of problems with support services- Implement and monitor corrective action plans4. Team management- Integrating, training and supporting new arrivals- Managing absenteeism, leave and conflicts- Conducting annual interviews- Define and monitor training plans- Keeping the multi-skilling grid up to date- Monitor indicators and management charts5. Quality, safety and compliance- Ensure compliance with safety instructions and GMP procedures- Use equipment in accordance with manufacturers' specifications- Work with the HSE and QA departments- Write and update documentation (procedures, fault reports, deviations, etc.)Profile required:- At least 2 years' higher education (bachelor's degree) or equivalent experience- 10+ years of experience in a pharmaceutical or industrial environment required- Knowledge of GMP and regulatory standards- Experience in continuous improvement (Lean, Kaizen, etc.)- Good knowledge of packaging equipment- Proficiency in Office Pack and ERP (ideally X3)- Leadership, ability to bring a team together- Initiative, autonomy and rigour- Ability to prioritise and react quickly- Good stress management and interpersonal skills