Scheduler mRNA Operations
Scheduler mRNA Operations
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Job Description
Work Schedule
Standard (MonFri)Environmental Conditions
OfficeJob Description
Thermo Fisher Scientific Inc. is the world leader in serving science with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier cleaner and safer. Whether our customers are accelerating life sciences research solving analytical challenges growing productivity in their laboratories improving patient health through diagnostics or the development and manufacture of lifechanging therapies we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies purchasing convenience and pharmaceutical services through our industryleading brands including Thermo Scientific Applied Biosystems Invitrogen Fisher Scientific Unity Lab Services Patheon and PPD.
The Monza site of Thermo Fisher Scientific is seeking for an Operations Scheduler for the mRNA Manufacturing Process Unit dedicated to formulation of mRNA Drug Substances & Drug Products.
The resource will be responsible for developing detailed planning for the manufacturing activities of the technical unit and related services aiming to achieve the units targets.
This role involves coordinating the readiness of the manufacturing department including the scheduling of:
new equipment installation and qualification in collaboration with the MSAT Equipment and Computer System Validation Automation and IT departments.
equipment maintenance and calibration activities working together with Maintenance and Calibration and Planning.
production material release process supporting the Supply Chain and Planning functions.
following the phases of processing optimizing times.
What will you do
Readiness:
Ensure the Manufacturing Units readiness concerning the shortterm production plan by optimizing the planning of all activities to guarantee plan identifying optimization margins and time reductions and managing realtime issues to minimize delivery impact. Specifically:
Monitor and ensure the of all activities necessary for production start (e.g. installation qualification maintenance and calibration activities of new and existing equipment).
Monitor and ensure the availability of approved documents (Protocols MBR SOP) within necessary timeframes.
Monitor the availability of approved materials within necessary timeframes in collaboration with Supply Chain & Planning MSAT and QC Raw Material & Packaging.
Scheduling:
Collaborate with the key stakeholders and planning to ensure optimal scheduling of manufacturing department activities issuing each single detailed batch scheduling informing all functions involved in the manufacturing activities.
Analyze the scheduling of all organizational unit activities identify short and mediumterm optimizations and work with planning to incorporate them into manufacturing plans.
Understand the scheduling of installation qualification maintenance and calibration activities of new and existing equipment including them into the manufacturing plans and monitoring/tracking their status.
Schedule Attainment:
Collaborate with MSAT and Manufacturing departments to ensure scheduled activities are carried out.
Monitor the of production activities through data/KPI collection and analysis and phase monitoring revising scheduling in case of issues to maintain delivery or interfacing with planning to assess impacts on planning.
Understand monitor and analyze microstoppages or events that have an impact.
Interface with QC for the of inprocess controls (IPC) within the planned timeframes.
Inform all relevant stakeholders in case of batch delays.
Standard Times:
Collaborate in defining standard times for the manufacturing activities in cooperation with involved functions.
Analyze and optimize standard times through performance monitoring and identifying improvements.
Account for activities in terms of productive staff work hours in the information system for accurate cost control.
Education/ Experience
MS in Operations Management Logistics Industrial Engineering or proven experience.
Knowledge Skills Abilities
Experience in main Upstream (Media Preparation and Enzymatic reactions in Bioreactors) and in Downstream steps (TFF Chromatography Encapsulation Clarifications/Filtrations).
Proven experience in scheduling project coordination roles.
Excellent organizational and time management skills.
Strong communication and interpersonal skills.
Proficiency in scheduling software and tools (e.g. Microsoft Project SAP).
Ability to work independently and as part of a team.
Detailoriented with the ability to handle multiple tasks simultaneously.
Problemsolving skills and a proactive approach to managing changes.
Thermo Fisher Scientific is an Equal Opportunity Employer.
Join us and be part of our Company
Employment Type
Full-Time
