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LI
Lilly Deutschland GmbH
10d ago

Site Molecule Steward(m/w/x)

Alzey
Full-timeOn-siteSenior

Description

As a technical leader in drug product manufacturing, you will oversee control strategies and provide expert guidance on production challenges to ensure the site meets all regulatory and quality standards.

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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

Education

Bachelor's degree

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

Languages

English – Business Fluent

Benefits

Ergonomic Workplace

  • •Workplace accommodation
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