QC MI&S Specialist (LIMS/ GMP Computer Systems)

Recruit Express Pte Ltd.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading recruitment firm is seeking a QC MI&S Specialist for its client in Singapore. The role entails ensuring data integrity and compliance with regulatory requirements in analytical instruments and software. Candidates should have experience in pharma manufacturing, GMP environments, and proficiency in QC systems like LIMS and TrackWise. A degree in a relevant field is required. Interested applicants should email their resumes to the provided contact person, Leon Leong.

Qualifications

• Experience in pharma manufacturing.
• Experience in MIS and LIMS operation in lab systems.
• Working experience within a regulated cGMP industry is a must.

Responsibilities

• Ensure data integrity by following regulatory requirements and policies.
• Complete QC analytical instrument and software validation deliverables.
• Write GMP procedures, validation documents and execute test scripts.

Skills

GMP

Project Management

Verbal Communication

Written Communication

Education

Bachelor or Master’s Degree in Microbiology, Biochemistry, Chemistry or Related Science Fields

Tools

TrackWise

LIMS

Empower

iLAB

MODA

C3ME

Job description

QC MI&S Specialist (LIMS/ GMP Computer Systems)

Singapore | Posted: Dec 15, 2025

Job Overview

QC MI&S Specialist

Key Requirements

• Office Hours: 5 days
• Experience in pharma manufacturing
• Experience in MIS (QC System, computerized systems) and LIMS operation in lab systems

Key Skills and Competencies

• Experience in GMP
• Experience in QC equipment qualification such as writing protocol
• Basic knowledge on regulatory requirement on equipment qualification
• Strong Project Management skill
• Good verbal and written communication skills

Responsibilities and Qualifications

• Our client is searching for an experienced Quality Control Validation Lead to join their QC computer systems validation team.
• Ensures data integrity by following regulatory requirements and policies pertaining to analytical instruments and computer software applications. Completes QC analytical instrument and software validation deliverables, writes GMP procedures, validation documents and executes test scripts. Approves final project documents and writes final validation summary reports.
• Minimum qualifications:
  • Min Bachelor or Master’s Degree. Preferred area of study in Microbiology, Biochemistry, Chemistry or Related Science Fields (Computer Sciences)
  • Working experience within a regulated cGMP industry is a must
  • Experience working in Quality Control Laboratory or enterprise computer systems. and GMP Quality Systems such as TrackWise, LIMS, iLAB, MODA, C3ME, and Empower would be at an advantage
  • Significant experience in Analytical Laboratory testing (ie: protein purification and characterization, protein chromatography, SDS-PAGE, Western blotting, and amino acid analysis, TOC, Bioburden, Endotoxin, Elisa, Flow cytometry, Microbiology).
  • Project manage

Contact

Interested candidates should drop your most updated resume to [e-mail] (Attn: QC Systems Specialist)

Leon Leong De Cong

Recruit Express Pte Ltd (Healthcare & Lifesciences Division)

EA License: 99C4599