Qc Environmental Monitoring Technician - Day Shift

Eli Lilly Eli Lilly · Pharma · Concord, NC

This role supports Parenteral Operations by performing environmental monitoring of manufacturing areas and utility sampling/analysis in a QC laboratory. It involves adherence to cGMP, training other technicians, and participating in continuous improvement projects. Requires a High School Diploma, 2+ years of relevant experience in GMP Pharmaceutical Manufacturing, and experience with Laboratory IT systems.

What you'd actually do

  1. Provide support for Parenteral Operations by performing environmental monitoring of the classified manufacturing areas and by performing utility sampling and analysis within the Parenteral Operations and QC Laboratory buildings.
  2. The QC Environmental Monitoring Technician will assist the QC Environmental Monitoring management with training other QC Environmental Monitoring Technicians and providing support in the manufacturing areas during routine environmental monitoring and utility sampling.
  3. Adhere to and promote compliance with all cGMP procedures, Quality Systems, and Good Documentation Practices.
  4. Provide support for Parenteral Operations activities by performing environmental monitoring of classified manufacturing areas.
  5. Provide support for manufacturing and laboratory activities by performing utility sampling and analysis within the Parenteral Operations and QC Laboratory buildings.

Skills

Required

  • High School Diploma or equivalent
  • 2+ years of demonstrated relevant experience in performing Environmental Monitoring in a GMP Pharmaceutical Manufacturing facility
  • Demonstrated ability in performing environmental monitoring techniques including, but not limited to viable surface monitoring, viable and non-viable air monitoring, compressed air monitoring, and water (potable, purified water, water for injection, clean steam) collection and analysis.
  • Previous experience with Laboratory IT systems such as LIMs, LES, and MODA.
  • Qualified applicants must be authorized to work in the United States on a full-time basis.

Nice to have

  • associate degree
  • preferably associated with aseptic production
  • Experience with cGMP requirements and regulatory compliance associated with a cGMP Manufacturing facility.
  • Strong interpersonal skills and ability to train/mentor QC Environmental Monitoring Technicians.
  • Strong oral and written communication skills
  • Ability to work in a lab environment including wearing appropriate PPE and other safety related equipment or considerations.
  • Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities.

What the JD emphasized

  • cGMP procedures
  • environmental monitoring
  • utility sampling and analysis
  • aseptic production
  • Laboratory IT systems