Production Planner

Experis Switzerland; Bezirk Solothurn; Vor Ort; CHF 75.000 - 110.000; Vollzeit

Zusammenfassung

Experis Switzerland is seeking a Production Planner to support manufacturing planning, scheduling, and changeover activities at the SOL DS Manufacturing Site in Solothurn. You will develop daily production schedules and medium-term plans used by Manufacturing, Materials, Quality, Engineering, Validation, and Plant Management.

The role requires at least an AA in a related field and 3–5 years of GMP experience, with the site location in Solothurn.

Qualifikationen

• Minimum Associate’s degree in Chemical/Biochemical Engineering, Supply Chain Management, or related field.
• Bachelor’s degree preferred.
• Minimum 3-5 years of relevant experience in a GMP regulated industry or an equivalent combination of education and experience.

Aufgaben

• Develops and maintains the site daily production schedules and medium-term production plans across multiple departments.
• Supports changeover activities and ensures alignment with demand.
• Confirms resource requirements and communicates constraints with suggested alternatives.
• Drives issue resolution for project success and reports status to team and management.
• Interacts with Manufacturing, Materials, Quality, Engineering, Validation, and Plant Management to coordinate planning activities.

Kenntnisse

Independent worker

Clear communication

Process improvement

Obstacle identification

GMP manufacturing

Biologics process knowledge

Influence without authority

Infor/Oracle familiarity

Excel macros

Planning and scheduling

Ausbildung

AA in Chemical/Biochemical Eng or related

Bachelor’s degree preferred

Tools

Infor

Oracle

Jobbeschreibung

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;
• Minimum 3-5 years of relevant experience in a GMP regulated industry or an equivalent combination of education and experience.

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.

Skills

• Independent worker with minimal supervision; customer focused and team player
• Clearly and actively communicates planning, scheduling and changeover information or process issues with affected parties in a timely manner.
• Ability to recognize opportunities for improvement in systems or processes and recommend solutions
• Ability to identify obstacles and upscale 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

Location: Solothurn

2 rounds of interviews.

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.