Lab QC Analyst - Microbial Testing / Bioburden / Validation (Up to $5000 x 14)

RECRUITFIRST PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading recruitment firm in Singapore is seeking a professional for laboratory operations to ensure compliance with ISO 17025 and cGMP. The role involves method development, validation, and acting as a technical reviewer for tests. Candidates should have 2-6 years of relevant experience in a regulated environment with a Bachelor’s degree in Science or a related field. Competitive salary and good benefits offered.

Benefits

Good Culture

Benefits

Qualifications

• Minimum 2-6 years of relevant QC microbiological experience in an ISO17025/GMP laboratory.
• Experience in method validation and development.
• Good understanding of regulatory guidelines.

Responsibilities

• Ensure laboratory operations meet ISO 17025 and cGMP requirements.
• Lead and perform method development and validation.
• Serve as Technical Reviewer for accredited tests.

Skills

QC microbiological experience

Knowledge of ISO 17025

Understanding of cGMP guidelines

Project Management

Measurement Uncertainty

Education

Bachelor of Science or related field

MSc. preferred

Job description

Up to $4500/mth

6 / 12 mth (can renew/convert)

Good Culture + Benefits!

Job Details

• Working hours: Office Hours

• Location: East

Job Descriptions

• Responsible for ensuring the laboratory operations in accordance to ISO 17025 and cGMP requirements
• Leads, designs and performs method development (i.e. bioassay and mycoplasma) and validation of new test procedures for incoming projects
• Functions as Technical Reviewer for A2LA accredited tests and non-accredited tests
• Evaluates analytical results to form interpretations of data and renders scientific opinions for client-driven projects
• Serves as subject matter expert (SME) in area of specialization, established standards for regulatory compliance
• 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 field; MSc. preferred but not essential
• Minimum 2-6 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
• Good understanding/working knowledge of Project Management and Measurement Uncertainty (MU)

*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.

RecruitFirst Pte Ltd E.A. 13C6342

Joseph Yap Shi Hao (R1767577)