(sr./principal) Ts/ms Engineer - Commercialization

Lilly

Minimum three years parenteral manufacturing experience
Gmp environment hands-on documentation management
Sterile product technology transfer leadership
The role involves leading and managing new parenteral product and process technology transfer projects alongside commercialization efforts

Job Summary

  • The role involves leading and managing new parenteral product and process technology transfer projects alongside commercialization efforts.
  • Candidates must possess at least three years of relevant experience working within a cGMP environment specifically for parenteral manufacturing.
  • The position requires active participation in development teams to implement TS/MS objectives while ensuring business and quality goals are met.

Matching Summary

The role involves leading and managing new parenteral product and process technology transfer projects alongside commercialization efforts.

Skills & Requirements

Must-have

  • Minimum three years parenteral manufacturing experience
  • GMP environment hands-on documentation management
  • Sterile product technology transfer leadership
  • Deviation investigation and root cause analysis
  • Regulatory submission and change control support

Nice-to-have

  • Strong analytical thinking and problem-solving skills
  • Ability to influence cross-functional teams
  • Excellent English written and oral communication
  • Experience with electronic document systems in GMP
  • Willingness to work overtime and travel

Key Requirements

  • 3+ years parenteral manufacturing site experience
  • In-depth knowledge of GMP regulations
  • Proven project management capabilities
  • Strong interpersonal and collaborative skills

Work Rights

Not specified

Tailored Resume

Cover Letter