Microbiology Laboratory Analyst/Specialist

Private Advertiser; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A distinguished pharmaceutical brand is seeking a Microbiological Laboratory Analyst/Specialist in Singapore to ensure high-quality standards in their manufacturing operations. This role involves conducting microbiological tests, environmental monitoring, and compliance with GMP standards, while supporting both the startup of a new facility and routine QC operations. Candidates should have a relevant Bachelor's degree and 3 to 5 years of experience in a GMP environment.

Benefits

Competitive salary

Professional development opportunities

Collaborative work environment

Qualifications

• 3 to 5 years of experience in microbiology within a pharmaceutical or GMP-regulated environment.
• Hands-on experience with microbial testing and equipment qualification.
• Experience in preparing for GMP inspections.

Responsibilities

• Assist in setting up the manufacturing plant and QC lab.
• Perform routine QC microbiological testing.
• Document testing activities in accordance with GMP guidelines.

Skills

Microbiological testing

Environmental monitoring

Equipment qualification

Data analysis

Problem-solving skills

Education

Bachelor Degree in Microbiology or related field

Job description

About

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 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 procedure 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 the 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.