Production Planner
Production Planner
- Art der Beschäftigung: Vollzeit
- 71.000 CHF – 86.000 CHF (von XING geschätzt)
- Hybrid
Production Planner
Über diesen Job
Production Planner
- Referenznummer: 637354
- Veröffentlicht am: 22 September 2026
- Anstellungsart: Temporärarbeit
- Eintrittsdatum:01.09.2026
- Industrie: Chemie und Biowissenschaften
- Pensum: Vollzeit
- Funktion:Andere
- Remote: Nein
Experis is recruiting a Production Planner to supports manufacturing planning, scheduling and changeover activities.
In this role, you will Develops the site manufacturing schedule for day to day operations and supports planning activities for long term timelines.
Summary
The incumbent supports manufacturing planning, scheduling and changeover activities for the SOL DS Manufacturing Site supporting both clinical and commercial programs and CQV phase. Responsible for creating and maintaining accurate, detailed daily production schedules and the medium-term production plans used by Manufacturing, Materials, Quality, Engineering, Validation and Plant Management. The incumbent also supports facility readiness, changeover and maintenance project schedules. Confirming resource requirements, proactively identifying and communicating constraints with suggested alternative solutions are also responsibilities of this position. The incumbent also drives issue resolution for project success and reports project status to team and manager.
Description
Develops the site manufacturing schedule for day to day operations and supports planning activities for long term timelines. Responsible for tactical day-to-day scheduling and product changeover timelines that meet the production demand plan. Interacts with manufacturing personnel to determine current completion state of production operation activities and to clarify any schedule updates/changes. Supports facility project schedules for shutdown work, commissioning, validation, change-over, routine/non-routine facilities maintenance activities.
Min Education and experience Requirements
- Minimum Associate’s degree (AA) in Chemical/Biochemical Engineering, Supply Chain Management, or related business/science/technical field;
- Bachelor’s degree (BS) preferred
- Minimum 3-5 years of relevant experience in a GMP regulated industry or an equivalent combination of education and experience.
- Independent worker with minimal supervision; customer focused and team player
• Ability to recognize opportunities for improvement in systems or processes and recommend solutions
• Ability to identify obstacles and escalate appropriately
• Working knowledge with planning and scheduling in a GMP manufacturing facility
• Understanding of protein biologics manufacturing process knowledge and related activities
• Recognizes and performs regular responsibilities, while pursuing learning of new skills and/or processes
• Ability to influence without authority, pro-actively builds healthy working relationships between their department and other groups
• Familiarity with enterprise applications (e.g. Infor, Oracle)
- Strong Experience with software packages (Office Package - Excel Macro)
Duration: 12 Months
2 rounds of interviews.