Sterile Product Manufacturing Expert

5 days ago


Brighton, Michigan, United States Bryllan LLC Full time

Bryllan LLC, a leader in Contract Manufacturing Organizations (CMOs), has an exciting opportunity for a Process Engineer to drive quality and efficiency in its manufacturing processes. This role involves supporting the development, transfer, and validation of manufacturing processes.

Main Responsibilities:
  1. Process Development: Support the development of manufacturing processes for sterile injectable pharmaceutical products.
  2. Cleaning Validation: Ensure cleaning validation standards are met throughout the transfer process.
  3. Technical Documentation: Develop and maintain technical documentation to support various steps in transferring products.

The successful candidate will have 2+ years of experience in the pharmaceutical industry, comprehensive knowledge of cGMP and regulatory principles, and a 4-year degree in Engineering, Science, or equivalent. Estimated salary: $90,000 - $130,000 per year.



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