Supply Chain – Detailed Scheduler
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Supply Chain Detailed Scheduler voor een biofarmaceutische organisatie in Breda, start 27 augustus 2026, min. 3 dagen per week on-site.
- Locatie
- Breda
- Werkvorm
- hybride
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Startdatum
- Eerste waarneming
- Opdrachtgever
- Global biopharmaceutical organization
Eisen
- Strong analytical and problem-solving skills
- Detail-oriented and able to coordinate multiple priorities
- Excellent interpersonal and collaborative skills
- Experience in supply chain planning within a GMP-regulated environment
- Ability to perform root cause analysis and work effectively in a team environment
- Willingness to work at least 3 days per week on-site in Breda
- Strong interest in standardization, process improvement and automation
Wensen
- Experience or interest in tools such as Tableau, Smartsheet, Databricks or RPA
Omschrijving
Our client is a global biopharmaceutical organization with a large manufacturing and supply chain operation in Breda. The site supports the production, packaging, storage and distribution of medicines to markets across Europe, Turkey, the Middle East and Africa, operating in a complex and highly regulated environment. As a Supply Chain – Detailed Scheduler, you will be responsible for managing short-term production planning for packaging lines and ensuring a stable and reliable supply of medicines. You will develop production plans, coordinate activities across departments and remove operational flow stoppers to support timely delivery. Working closely with manufacturing, quality, warehouse and supply chain teams, you will also contribute to continuous improvement, standardization and process automation within the supply planning organization. Key responsibilities include managing short-term production planning for packaging lines, creating production plans, managing orders and supporting product launches and phase-in/phase-out activities, monitoring supply chain performance and proactively removing flow stoppers, measuring weekly and monthly KPIs including MPS stability and driving improvement actions, facilitating daily operational meetings, leading weekly capacity meetings with manufacturing, quality, warehouse and supply chain stakeholders, driving standardization, simplification and automation of planning processes, leading continuous improvement initiatives and root cause analyses, collaborating cross-functionally to ensure realistic and achievable supply plans, and ensuring stable operations and supply chain efficiency while working within GMP and GDP guidelines. Requirements include experience in supply chain planning within a GMP-regulated environment, strong analytical and problem-solving skills, excellent interpersonal and collaborative skills, ability to perform root cause analysis and work effectively in a team environment, strong interest in standardization, process improvement and automation, experience or interest in tools such as Tableau, Smartsheet, Databricks or RPA is preferred, detail-oriented and able to coordinate multiple priorities, and willingness to work at least 3 days per week on-site in Breda.
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