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 : www.akkodis.com
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 plan
- Issue production orders (PO)
- Ensure availability of materials and equipment
2. Production monitoring
- Guarantee compliance with the schedule
- Manage production contingencies (early/late)
- Actively participate in production meetings
- Coordinate technical and external interventions
3. Continuous improvement
- Leading continuous improvement initiatives (Lean, Kaizen, etc.)
- Analyse the root causes of problems with support services
- Implement and monitor corrective action plans
4. 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 charts
5. 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