Akkodis, is a global leader in the engineering and R&D 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 :
Note : 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 deadlines
Leading and supervising a production team as part of a continuous improvement process.
Key responsibilities :
1. Operations planning
Drawing up the short-term production planIssue production orders (PO)Ensure availability of materials and equipment2. Production monitoring
Guarantee compliance with the scheduleManage production contingencies (early / late)Actively participate in production meetingsCoordinate technical and external interventions3. Continuous improvement
Leading continuous improvement initiatives (Lean, Kaizen, etc.)Analyse the root causes of problems with support servicesImplement and monitor corrective action plans4. Team management
Integrating, training and supporting new arrivalsManaging absenteeism, leave and conflictsConducting annual interviewsDefine and monitor training plansKeeping the multi-skilling grid up to dateMonitor indicators and management charts5. Quality, safety and compliance
Ensure compliance with safety instructions and GMP proceduresUse equipment in accordance with manufacturers' specificationsWork with the HSE and QA departmentsWrite and update documentation (procedures, fault reports, deviations, etc.)Profile required :
At least 2 years' higher education (bachelor's degree) or equivalent experience10+ years of experience in a pharmaceutical or industrial environment requiredKnowledge of GMP and regulatory standardsExperience in continuous improvement (Lean, Kaizen, etc.)Good knowledge of packaging equipmentProficiency in Office Pack and ERP (ideally X3)Leadership, ability to bring a team togetherInitiative, autonomy and rigourAbility to prioritise and react quicklyGood stress management and interpersonal skills