Demand & Supply Planner
Key information
- Publication date:28 May 2025
- Workload:100%
- Contract type:Permanent position
- Place of work:Genève
Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane strength is to offer a global patient care. Using its products, practitioners are able to fill all kinds of wrinkles, from the finest to the deepest, to restore youthful volume to the face, and to treat the neck and décolleté, with natural results. The strength of Teoxane is also its human size and independence. Teoxane has a total freedom of thoughts, action and innovation which makes the company unique.
In the frame of the growth of our business, we are looking for a:
Demand & Supply Planner
Main responsibilities:
- Lead the demand planning process in coordination with Global and Local sales, Marketing and Finance teams.
- Develop and optimize supply plans (short, mid and long term).
- Manage inventory levels while ensuring high service levels.
- Analyze forecast accuracy and implement corrective actions when needed.
- Collaborate closely with Operations, Logistics and Distributors to ensure product availability.
- Monitor Demand & Supply planning activities to ensure achievement at performance level expected for related key indicators: Forecast accuracy Bias, stock cover, OTIF.
- Build and drive improvement initiatives in planning tools and methods related to Demand and Inventory Planning.
- Participate in end-to-end supply chain and operations projects.
- Any other special mission that may be entrusted by the direction.
Your profile:
- Master's degree in Supply Chain, Logistics or a related field.
- 5-7 years of experience in a similar role preferably within pharmaceutical/MD, or cosmetics industry.
- Supply Chain certifications (APICS) is a plus.
- Proficient in planning tools (SAP, or other APS systems).
- Proficient in using Microsoft pack office (especially Excel/ PowerBI).
- Experience working in an international environment.
- Familiarity with medical regulatory standards (ISO 13485, MDR) is a strong plus.
- Strong organizational and analytical skills with a proactive mindset.
- Excellent interpersonal and cross-functional collaboration skills.
- Fluency in English / French.