Responsibilities
Serve as the primary point of contact for daily management of the finite production schedule across manufacturing and facility operations.
Coordinate activities between Operations, Process Engineering, Automation, Facility Engineering, Microbiology, and other key functions.
Participate in daily Tier 1 and Tier 2 meetings and update the schedule accordingly.
Align the Site Plan of Record with the Finite Schedule and support scenario planning for new product introductions.
Enable smooth execution of activities across Manufacturing, Engineering, Calibration, Labs, and Warehouse teams.
Collaborate with network experts to expand RTMS functionality and develop operational models for fed-batch and continuous manufacturing.
Support capacity planning, debottlenecking, and utilization strategy with cross-functional partners.
Assess and mitigate schedule impacts from unforeseen events.
Drive schedule adherence, escalate issues when needed, and ensure full resource allocation across teams.
Qualifications
Educational background in a relevant scientific or engineering discipline.
2–5 years of GMP biologics manufacturing experience (upstream or downstream).
Strong problem-solving skills and ability to perform under pressure in a complex GMP environment.
Fluent English (C1) and proficient German (B2) communication skills.
Bachelor’s or Master’s degree in a relevant field.
Experience with SAP, MES, and scheduling tools.
Ability to work effectively in teams and manage independent projects.
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