Quality Control Analyst I, Microbiology

Proclinical; Norton (MA); Presencial; GBP 33.000 - 48.000; Jornada completa

Descripción de la vacante

Proclinical is seeking a Quality Control Analyst I to join a GMP manufacturing environment. This entry-level role focuses on routine environmental monitoring and critical utility sampling to support production of critical therapies.

The candidate will perform QC testing (TOC, conductivity, bioburden, endotoxin) and microbial identification using MALDI-TOF, while contributing to SOP authoring and data trending. On-site role with domestic travel between Norton, MA and Cambridge, MA may be required.

Formación

• Bachelor of Science in Microbiology, Biology or Biochemistry.
• 0–2 years of GMP laboratory experience.
• Ability to travel between domestic sites (Norton, MA and Cambridge, MA).
• On-site work is required.

Responsabilidades

• Perform routine environmental monitoring (EM) and critical utility (CU) sampling and testing at the GMP manufacturing site.
• Support the raw material program through inspection of material.
• Perform water, gas and environmental sampling within a cleanroom facility.
• Perform QC testing (TOC, conductivity, bioburden, endotoxin).
• Perform microbial counting and identification using MALDI-TOF instrumentation.
• Author and review technical documentation (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.

Conocimientos

Environmental monitoring

Microbiology techniques

GMP laboratory practices

Educación

Bachelor of Science Degree in scientific discipline (e.g. Microbiology, Biology, Biochemistry)

Herramientas

MALDI-TOF instrumentation

Descripción del empleo

Quality Control Analyst I - Contract - Norton, MA

Ready to launch your microbiology career in a GMP environment where your work directly supports the production of critical therapies?

Proclinical is hiring a Quality Control Analyst I - Microbiology to join our client's team in the US. The position requires flexibility with changing priorities.

Primary Responsibilities:

The successful candidate will be primarily responsible for performing 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.

Skills & Requirements:

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

The Quality Control Analyst I's responsibilities will be:

• Supporting the EM/CU program at the GMP manufacturing site at the Norton facility
• 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