QC Analyst I, Microbiology – GMP Lab (Contract)

Proclinical; Norton (VA); Presencial; USD 55.000 - 70.000; Tempo integral

Resumo da vaga

Proclinical is seeking a Quality Control Analyst I - Microbiology on a contract basis for our client in the US. The role focuses on routine environmental monitoring and critical utility sampling in a GMP manufacturing setting, with travel between Norton, MA and Cambridge, MA.

You will perform water, gas and environmental sampling in cleanrooms, run QC tests (TOC, conductivity, bioburden, endotoxin), and assist with documentation, data trending and raw material inspections as needed.

Qualificações

• Bachelor of Science in a scientific discipline (e.g. Microbiology, Biology, Biochemistry).
• 0-2 years of GMP laboratory experience.
• Ability to travel between Norton, MA and Cambridge, MA.
• On-site support is required.

Responsabilidades

• Perform routine environmental monitoring (EM) and critical utility (CU) sampling and testing in support of GMP manufacturing.
• Secondary responsibility supporting the raw material program through inspection of material.
• Perform water, gas and environmental sampling within a cleanroom facility.
• Perform QC testing (i.e., TOC, conductivity, bioburden, endotoxin).
• Perform microbial counting and identification using MALDI-TOF instrumentation.
• Author and review technical documentation (e.g. SOPs, protocols, reports).
• Support and maintain data for trending analysis
• Secondary support for Raw Material visual inspection and sampling
• Additional project work or duties as assigned

Formação

Bachelor of Science Degree in Microbiology/Biology/Biochemistry

GMP Laboratory Experience (0-2 years)

Descrição da vaga

Proclinical is seeking a Quality Control Analyst I - Microbiology on a contract basis for our client in the US. The role focuses on routine environmental monitoring and critical utility sampling in a GMP manufacturing setting, with travel between Norton, MA and Cambridge, MA.

You will perform water, gas and environmental sampling in cleanrooms, run QC tests (TOC, conductivity, bioburden, endotoxin), and assist with documentation, data trending and raw material inspections as needed.