QC Environmental Monitoring Analyst - Cleanroom GMP (Shift)

Lonza; Singapore; On-site; SGD 42,000 - 72,000; Full time

Benefits offered by this job

Medical insurance

Transport from MRT to site

Global exposure

Job summary

Lonza Singapore is seeking an Analyst QC, Environmental Monitoring to perform air, surface, viable and non-viable sampling across manufacturing and cleanroom areas, ensuring GMP quality and safety standards.

You will analyze raw materials, in-process, environmental and final product samples per SOPs and GMP requirements, document results with data integrity, support investigations and deviations, maintain lab operations, and contribute to continuous improvement while working on site.

Qualifications

• Degree in science or related field.
• Relevant work experience in Pharmaceutical Manufacturing or Biopharmaceutical industry.
• Familiar with Regulatory requirements and local codes & standards (FDA, EMEA, ICH Q7).
• Knowledge of quality management system requirements in GMP facilities.

Responsibilities

• Perform environmental monitoring (air, surface, viable, non‑viable) across manufacturing and cleanroom areas.
• Analyze environmental, in‑process, raw material and final product samples per SOPs and GMP requirements.
• Document, review and report results with data integrity.
• Support trending, investigations, deviations/OOS and root cause analysis.
• Maintain laboratory operations including equipment upkeep, reagents, consumables and inventory.
• Manage sample logistics and QC documentation/shipping.

Skills

GMP knowledge

Quality management

Regulatory compliance

Team player

Safety focus

Education

Bachelor's degree in science

Job description

Lonza Singapore is seeking an Analyst QC, Environmental Monitoring to perform air, surface, viable and non-viable sampling across manufacturing and cleanroom areas, ensuring GMP quality and safety standards.

You will analyze raw materials, in-process, environmental and final product samples per SOPs and GMP requirements, document results with data integrity, support investigations and deviations, maintain lab operations, and contribute to continuous improvement while working on site.