Quality Control Technician

NUSANTARA PRIME CONSULTING PTE. LTD.

Singapore

On-site

SGD 28,000 - 42,000

Full time

3 days ago

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Job summary

NUSANTARA PRIME CONSULTING PTE. LTD. in Singapore invites a detail-oriented lab support professional to assist in day-to-day laboratory operations, including documentation, sample handling, and equipment upkeep.

You will work under GMP guidelines, maintain training records, and contribute to continuous improvement initiatives while ensuring accurate data management and timely execution of tasks.

Qualifications

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.
Candidates who do not fulfill the education background but possess laboratory experience can be accepted.
Fresh graduates with positive attributes will be considered.
Possess basic laboratory skills such as pipetting, glassware management and laboratory safety.
Have GMP manufacturing knowledge.
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.
Excellent attention to details.
Good time management and project management skills.

Responsibilities

To support laboratory operations including filing/archival, receipt of media, autoclaving of consumables.
To support LIMS/LES coordinator roles.
To perform check for documentation completeness for basic instruments, equipment or testing/calibrations.
To perform cleaning and disinfection of laboratory instruments, controlled temperature units and equipment.
To perform, preventative maintenance of laboratory instruments/equipment.
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 Manager.

Skills

Pipetting

Glassware management

Laboratory safety

LIMS

MS Word

MS Excel

PowerPoint

Independence

Time management

Project management

Interpersonal skills

Attention to detail

Education

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

Tools

LIMS/LES

Job description

Job Responsibilities:

To support laboratory operations(not limited to) e.g., filing/archival, receipt of media, autoclaving of consumables
To support LIMS/LES coordinator roles
To perform check for documentation completeness for basic instruments, equipment or testing/calibrations
To perform cleaning and disinfection of laboratory instruments, controlled temperature units and equipment
To perform, preventative maintenance of laboratory instruments/equipment
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 Manager

Job Requirements:

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.
Candidates who do not fulfill the education background but possess laboratory experience can be accepted.
Fresh graduates with positive attributes will be considered.
Possess basic laboratory skills such as pipetting, glassware management and laboratory safety.
Have GMP manufacturing knowledge.
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
Excellent attention to details
Good time management and project management skills