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LILilly Deutschland GmbH

Site Molecule Steward(m/w/x)

Alzey
Full-timeOn-siteSenior

Technical leadership for parenteral drug product manufacturing, implementing site control strategies at a global healthcare leader. Bachelor's degree in science or engineering and parenteral product manufacturing experience required. Workplace accommodation provided.

Requirements

  • Bachelor's degree in science or engineering
  • Experience supporting parenteral product manufacturing
  • Strong communication skills
  • Ability to prioritize and multi-task
  • Collaboration with cross-functional teams

Tasks

  • Act as the technical subject matter expert for drug product manufacturing
  • Provide technical leadership for TS/MS projects
  • Own the implementation of site control strategies
  • Collaborate with parenteral network peers in QA, QC, and Engineering
  • Coordinate regularly with drug substance counterparts
  • Align technical strategies with quality and regulatory guidance
  • Investigate product performance with a curious and analytical mindset
  • Coach site staff to build technical capabilities
  • Direct responses to deviations and production challenges
  • Assess the impact of manufacturing change controls
  • Represent the TS/MS function during regulatory interactions
  • Monitor and implement external corporate technical trends
  • Transfer technical knowledge across all organizational levels
  • Influence cross-functional teams to meet business objectives

Education

  • Bachelor's degree

Languages

  • EnglishBusiness Fluent

Benefits

Ergonomic Workplace

  • Workplace accommodation
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lilly Deutschland GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.

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