Microbiology Laboratory Analyst/Specialist

Jobstreet SG; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A distinguished pharmaceutical brand is seeking a skilled Microbiology Laboratory Analyst/Specialist in Singapore. This role ensures high-quality standards in microbiological testing and supports both the startup of a new facility and routine QC operations. Candidates must have a Bachelor degree in a related field and 3 to 5 years of experience in a GMP environment. The position offers a competitive salary and opportunities for professional development.

Benefits

Competitive salary and benefits package

Opportunities for professional development

Dynamic and collaborative work environment

Qualifications

• Minimum of 3 to 5 years of experience in microbiology within a pharmaceutical or GMP-regulated environment.
• Hands-on experience with microbiological testing and equipment qualification.
• Knowledge of microbiological data analysis and reporting.

Responsibilities

• Assist in the setup of the new manufacturing plant and QC lab.
• Perform routine QC microbiological testing on various samples.
• Write Standard Operating Procedures (SOPs) and testing methods.

Skills

Microbiological testing

Equipment qualification

Environmental monitoring

Data analysis

Problem-solving

Attention to detail

Education

Bachelor degree in Microbiology, Biotechnology, Pharmaceutical Sciences, or related field

Job description

Microbiology Laboratory Analyst/Specialist

We are a distinguished pharmaceutical brand with over sixty years of expertise, now expanding regionally in Singapore as our Southeast Asia hub. We are seeking a skilled Microbiological Laboratory Analyst/Specialist to ensure the high standards of quality control in our manufacturing operations, supporting both the startup of a new facility and routine QC operations. This role will involve performing microbiological tests, environmental monitoring, and method validation among others to ensure compliance with GMP, regulatory standards, and internal quality policies.

Responsibilities

Startup Phase

• Assist in the setup of the new manufacturing plant and QC lab, ensuring all necessary equipment, materials, testing methods, and procedures are in place for smooth operations.
• Collaborate with teams to source materials, equipment, and contract laboratories to support microbiological testing and manufacturing needs.
• Develop and lead Environmental Monitoring (EM) qualification programs and utilities qualification to ensure facility cleanliness and microbial control per GMP standards.
• Conduct microbiological testing-related equipment qualification and method verification to meet GMP standards.
• Assist with chemistry method validation/verification activities to meet GMP standards, where necessary.
• Support the establishment of QC operations, ensuring QC readiness to support testing and release for raw materials, in-process samples, finished products, and environmental samples.
• Support preparations for Health Sciences Authority (HSA) GMP inspections to ensure compliance.

Routine Operations

• Perform routine QC microbiological testing on raw materials, in-process samples, finished products, and environmental samples.
• Assist in troubleshooting microbiological issues and implement corrective actions when needed.
• Ensure proper maintenance, calibration, and qualification of microbiological equipment in the lab.
• Document testing and activities in accordance with GMP guidelines, maintaining accurate records.
• Write Standard Operating Procedures (SOPs) and testing methods to ensure continued compliance.
• Stay updated on new microbiological techniques and regulatory changes to maintain high laboratory standards.

Qualifications & Skills

• Bachelor degree in Microbiology, Biotechnology, Pharmaceutical Sciences, or a related field.
• Minimum of 3 to 5 years of experience in microbiology within a pharmaceutical or GMP-regulated manufacturing environment.
• Hands‑on experience with microbiological testing, equipment qualification, and environmental monitoring in a QC lab.
• Strong understanding of QC equipment qualification and validation processes.
• Familiarity with environmental monitoring (EM) programs and utilities qualification in pharmaceutical manufacturing.
• Knowledge of microbiological data analysis, interpretation, and reporting.
• Experience in preparing for and supporting GMP inspections is highly desirable.
• Excellent attention to detail, communication, and problem‑solving skills.

What We Offer

• Competitive salary and benefits package.
• Opportunities for professional development and advancement.
• A dynamic and collaborative work environment.