QC Environmental Monitoring Analyst
Core
Perform scientific procedures and environmental monitoring in biopharmaceutical cleanroom environments to ensure product safety and compliance.
Role type
QC Environmental Monitoring Analyst
Builds
Robust environmental monitoring programs for biopharmaceutical manufacturing clients
Domain
Biopharmaceuticals / GMP / Cleanroom Operations
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP compliance, aseptic techniques, viable and non-viable air monitoring, surface sampling, water and steam system sampling, compressed gas monitoring, anomaly investigation, documentation, data recording
Preferred skills
Microbiology or Biochemistry background, cleanroom experience, analytical thinking, problem-solving, shift flexibility
Technologies
ISO 7, ISO 8, GMP
Responsibilities
Conduct routine Environmental Monitoring within ISO 7 and ISO 8 biopharmaceutical cleanroom environments, perform viable and non‑viable sampling and incubation activities, complete sampling of Ethanol, Water for Injection (WFI), and Clean Steam systems, support investigations by completing ad‑hoc sampling and swabbing, maintain accurate compliant documentation aligned with GMP requirements, report and investigate anomalous or quality-related events, support manufacturing operations by completing post‑shutdown and response Environmental Monitoring
Seniority
Junior to Senior, hands-on IC
