Clinical Master Production Scheduler (m/f/d)

Clinical Master Production Scheduler (m/f/d)

Informatik / Telekommunikation
  • Temporär - Vollzeit
  • Referenz : INT-051252
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  • Region Basel
  • Art des Vertrags Temporär - Vollzeit
  • Tätigkeitssektor Informatik / Telekommunikation


As a preferred supplier for Roche in Kaiseraugst, we are looking for an individual as

Clinical Master Production Scheduler (m/f/d) 

with contract for 1 year and with possible extension. The earliest start date is asap or by 01.12.2023.  Home office is offerred, but one must work on campus majority of the time.


Tasks & Responsibilities:

• Manage and – if needed – escalate supply constraints. Analyze and suggest options to close supply gaps considering financial impact and timelines.
• Maintain schedule stability considering material availability and capacity requirements based on planning and demand time fences.
• Responsible for detailed scheduling of Packaging activities and ensuring ‘readiness' for a given packaging activity in close coordination with various support groups and Manufacturing. This can include detailed scheduling of orders, ensuring materials are available upon order release, and releasing orders to allow the shop floor to execute.
• Support global alignment & harmonization over the manufacturing sites.
• Monitoring production output and comparing it to the supply plan, e.g. production plan performance. Identify differences and drive solutions to mitigate those variances.
• Owner and facilitator of weekly Readiness and Scheduling Meetings. Decide which orders have to be moved, pulled in or deleted and commit the final production plan.
• Provide input to management in order to optimize resources, capacity and capabilities and meet objectives for manufacturing efficiencies, inventory levels and customer service.
• Accountable for managing the site master production schedule that accounts for production demand (i.e. IMP material) and non-production demand (i.e. Maintenance, Validation, Engineering).
• Perform ‘what if' scenario analyses to support Site & Global priorities (i.e. Site operational capabilities and Clinical network decisions).
• Represent the respective site performance metrics as well as the site capacity and capabilities in the Clinical Demand and Operation Supply Review to enable decision making.
• Own, manage and level load of order volume to meet the supply capacity in 8 weeks horizon.
• Manage, prioritize and decide on Order Change Requests according to customer requests and depending on site capacity.
• Actively leads or participates in global and local Projects and Kaizens to optimize Clinical Supply.
• Participates proactively in weekly team huddles to support key performance indicator (KPI) tracking and Continuous Improvement. Works independently and self-motivated on ideas for process improvements and its implementation according to the Roche PT Lean Production System (LPS) initiative.

Erforderliches Profil

Must Haves:

• University degree or equivalent diploma, preferably in Business (Economics, Operations Management, Supply Chain Management), Life Sciences or Engineering. Master degree is a plus.
• APICS and/or SCOR certification, or associated relevant experience ****
• Min. 3 years of work experience in the GMP environment (e.g. pharmaceutical or food industry), experience in a supply chain function is preferred ****
• ERP system experience, e.g. SAP, OMP or APO ****
• Experience in project management and in a cross-functional and cross-cultural environment ****
• Demonstrated (matrix) leadership experience or stakeholder management experience in a changing environment ****
• Knowledge and application of production efficiency methodologies (5S, Lean Manufacturing, Six Sigma, and/or Theory of Constraints)
• Knowledge of Supply Chain Management with focus on Scheduling, Capacity, Capabilities and Resource Planning (including supply chain optimization)
• Knowledge of support groups to effectively perform tasks, eg clinical packaging, production enablement, planning, quality and clinical distribution
• Excellent verbal/written communication and presentation skills in English and German


• Strong planning, organization, and time-management skills to support multiple teams and projects with effective prioritization
• Independent self-starter, with ability to perform work without supervision and show good judgment in determining objectives and approaches to assignments
• Effectively lead or facilitate formal and informal teams to develop robust solutions for supply / demand constraints and process improvement
• Strong analytical, logic and problem solving skills
• Ability to communicate with multiple stakeholders, simplify what is complex, focus on key messages and experience in communicating with senior leadership representatives.
• Ability to positively influence key decision-makers.
• Collaborative and agile mindset actively looking to make contributions to cross-functional teams and to develop self-directed team organization

Nice to Have:

• PMP/Operational Excellence/Six Sigma/Lean training
• Experience in clinical operations, technical drug development, regulatory or quality

Application process

Interested? You can find more information here: Infopackage. Please apply via the "Bewerben" button below and answer all questions, otherwise we will be unable to process your application. Please upload your CV in English along with your degree certificate and latest reference letter.


  • Agentur GPP AG - GLOBAL RECRUITMENT - +41 44 266 50 25
  • Veröffentlicht am 4. September 2023
  • Berater-in Claudia Zah