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

Eli Lilly UK

United Kingdom
**
New product/process technology transfer
Process improvements
Post-approval changes
** Eli Lilly is seeking a (Sr./Principal) TS/MS Engineer for Commercialization to manage and lead projects related to new product and process technology transfers in a cGMP environment. The ideal candidate will have at least three years of relevant experience, strong analytical and communication skills, and be able to work collaboratively in a fast-paced environment. **

Job Summary

  • Lead and manage new parenteral product/process tech transfer & commercialization projects, including development technical study, the required support to regulatory registration, post approval changes and process improvements.
  • Prepare, review, approve and provide technical support for preparation of relevant technical documents, with hands-on experience to managing the documentation under electronic systems in a GMP environment as required.
  • Follow various HSE management procedures and fulfil the work safety responsibilities.

Matching Summary

Match Score: 75

** Eli Lilly is seeking a (Sr./Principal) TS/MS Engineer for Commercialization to manage and lead projects related to new product and process technology transfers in a cGMP environment. The ideal candidate will have at least three years of relevant experience, strong analytical and communication skills, and be able to work collaboratively in a fast-paced environment. **

Skills & Requirements

Must-have

  • new product/process technology transfer
  • process improvements
  • post-approval changes
  • deviation investigation
  • regulatory registration support
  • parenteral manufacturing

Nice-to-have

  • analytical thinking
  • multi-tasking
  • decision-making
  • problem-solving
  • learning agility
  • project management
  • influencing skills
  • leading projects
  • cross-departmental collaboration
  • interpersonal skills

Key Requirements

  • Minimum three years of relevant experience in parenteral manufacturing site within a cGMP environment
  • Knowledgeable with GMP
  • Experienced in parenteral manufacturing
  • Good English communication skills
  • Good computer skills
  • Good written and oral communications

Work Rights

Not specified

Tailored Resume

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