QC Technician

WUXI XDC SINGAPORE PRIVATE LIMITED; Singapore; On-site; SGD 39,000 - 73,000; Full time

Job summary

WUXI XDC SINGAPORE PRIVATE LIMITED is seeking a laboratory professional to conduct microbiological and physiochemical testing in a cGMP environment. You will monitor clean utilities, classify cleanrooms, and support aseptic simulations.

The role requires a Diploma in Life Science or equivalent and 1–2 years in pharma/medical devices labs, with knowledge of pharmacopoeias and GMP practices. Strong basic lab skills and MS Office proficiency are expected.

Qualifications

• Min Diploma in Life Science, Process Technology, Pharmaceutical Sciences or equivalent.
• 1-2 years of experience in the pharmaceutical or medical devices industry, with experience on working in a laboratory environment preferred
• Familiar with PICS, ICH, Singapore HSA, FDA, EMA, NMPA, WHO technical guideline and USP, Eur.P, ChP pharmacopoeias.
• Preferred to have knowledge on GMP manufacturing.
• Basic laboratory skills such as pipetting, glassware management and laboratory safety.
• Attended courses associated with microbiology
• Basic proficiencies in digital literacies such as Microsoft Word, Excel, PowerPoint
• Ability to work independently and follow critical timelines
• Ability to adapt to a changing work environment
• Effective interpersonal skills at all internal and external levels

Responsibilities

• To perform quality control microbiological testing of raw materials, under cGMP conditions.
• To perform physiochemical testing of pharmaceutical water samples
• To perform monitoring for the facility clean utilities system e.g.
• To perform monitoring for classified cleanrooms, clean air devices and personnel.
• To perform non-routine sampling and testing for microbiological investigations.
• To perform cleaning and disinfection of laboratory instruments, controlled temperature units and equipment
• To perform, preventative maintenance of laboratory instruments/equipment
• To support aseptic process simulations
• To manage microbiological inventory required for sampling and testing
• To ensure adherence to ALCOA principles for managing laboratory data
• To adhere to site/job role training plan, and maintain individual training records
• To support continuous improvement initiatives
• To maintain laboratory housekeeping using 5S approach
• Ensure timely escalation of investigations accidents, near misses and breaches of policies
• To carry out tasks required by the reporting Manage

Education

Diploma in Life Science, Process Technology, Pharmaceutical Sciences or equivalent

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Job Responsibilities：

• To perform quality control microbiological testing of raw materials, under cGMP conditions

• To perform physiochemical testing of pharmaceutical water samples

• To perform monitoring for the facility clean utilities system e.g.

• To perform monitoring for classified cleanrooms, clean air devices and personnel.

• To perform non-routine sampling and testing for microbiological investigations.

• To perform cleaning and disinfection of laboratory instruments, controlled temperature units and equipment

• To perform, preventative maintenance of laboratory instruments/equipment

• To support aseptic process simulations

• To manage microbiological inventory required for sampling and testing

• To ensure adherence to ALCOA principles for managing laboratory data

• To adhere to site/job role training plan, and maintain individual training records

• To support continuous improvement initiatives

• To maintain laboratory housekeeping using 5S approach

• Ensure timely escalation of investigations accidents, near misses and breaches of policies

• To carry out tasks required by the reporting Manage

Requirements:

• Min Diploma in Life Science, Process Technology, Pharmaceutical Sciences or equivalent.

• 1-2 years of experience in the pharmaceutical or medical devices industry, with experience on working in a laboratory environment preferred

• Familiar with PICS, ICH, Singapore HSA, FDA, EMA, NMPA, WHO technical guideline and USP, Eur.P, ChP pharmacopoeias.

• Preferred to have knowledge on GMP manufacturing.

• Basic laboratory skills such as pipetting, glassware management and laboratory safety.

• Attended courses associated with microbiology

• Basic proficiencies in digital literacies such as Microsoft Word, Excel, PowerPoint

• Ability to work independently and follow critical timelines

• Ability to adapt to a changing work environment

• Effective interpersonal skills at all internal and external levels