Junior Lab Analyst - Microbial / Bioburden / Validation (Up to $3600 x 14)

RecruitFirst; Singapore; On-site; SGD 3,000 - 4,000; Full time

Job summary

A leading recruitment agency in Singapore is seeking a Junior Lab Analyst to ensure laboratory operations comply with ISO 17025 and cGMP standards. Responsibilities include method development, data evaluation, and technical liaison with clients. The ideal candidate should possess a Bachelor of Science and have 1-2 years' relevant experience in a QC microbiological lab. The position offers a competitive salary package.

Qualifications

• Minimum 1-2 years of relevant QC microbiological experience in an ISO17025/GMP laboratory environment.
• Experience in method validation and development.
• Knowledge of regulatory guidelines.

Responsibilities

• Ensure laboratory operations comply with ISO 17025 and cGMP requirements.
• Perform method development and validation for tests.
• Evaluate analytical results and provide scientific opinions.

Skills

Method validation

Good knowledge of ISO 17025

cGMP compliance

Analytical interpretation

Education

Bachelor of Science or related discipline

Job description

Junior Lab Analyst - Microbial / Bioburden / Validation (Up to $3600 x 14)

Responsible for ensuring the laboratory operations in accordance to ISO 17025 and cGMP requirements.

Performs method development (i.e. bioassay and mycoplasma) and validation of new test procedures for incoming projects.

Evaluates analytical results to form interpretations of data and renders scientific opinions for client-driven projects.

Serves as technical liaison with Customers with regards to technical services and performs Customer site visits where required.

Participates in internal Quality Audits, System Audits, Audits conducted by external agencies and Regulatory Authorities.

Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements.

Requirements

• Bachelor of Science or any related in any science discipline.
• Minimum 1-2 years of relevant QC microbiological experience working in an ISO17025/GMP laboratory environment.
• Experience in method validation and development, method transfer, qualification activities in regulated laboratory.
• Good knowledge of ISO 17025, cGMP and other regulatory guidelines.

Interested applicants, please apply with your resume with reason(s) for leaving previous employment(s), notice period, last drawn and expected salary.

All applications will be treated with strictest confidentiality. We regret that only shortlisted candidates will be notified.