QC Lab Specialist - GMP & Continuous Improvement

No deviation Pte Ltd; Singapore; On-site; SGD 45,000 - 75,000; Full time

Benefits offered by this job

Generous Leave Policy

Health & Wellness Coverage

Professional Development

Inclusive Culture

Impactful Work

Job summary

No deviation Pte Ltd is seeking a qualified QC Laboratory support role to ensure equipment reliability, documentation integrity, and GMP compliance in the QC department. This position assists with calibration, maintenance, and qualification of laboratory instruments, coordinates vendor servicing activities, and supports the broader equipment lifecycle from documentation to qualification.

You will participate in investigations, deviations, CAPA, and other quality system activities while

Qualifications

• Diploma or degree in science, chemistry, biology, pharmacy, or related field.
• Prior QC lab or GMP-regulated experience preferred.
• Familiarity with calibration, maintenance, and qualification of laboratory equipment.
• Knowledge of GMP, Data Integrity, change control, deviations, CAPA.
• Strong attention to detail and documentation accuracy.
• Good organizational and vendor coordination skills.

Responsibilities

• Support routine calibration, maintenance, and qualification of laboratory instruments.
• Coordinate equipment servicing and vendor maintenance activities.
• Maintain documentation, SOPs, forms, and laboratory records.
• Initiate and manage change controls, deviations, and CAPA with GMP compliance.
• Assist in audits, investigations, and continuous improvement initiatives.

Skills

Attention to detail

Documentation

Communication

Team coordination

Education

Diploma/Degree in Science or related

Tools

LIMS

MS Office

Calibration tools

Job description

No deviation Pte Ltd is seeking a qualified QC Laboratory support role to ensure equipment reliability, documentation integrity, and GMP compliance in the QC department. This position assists with calibration, maintenance, and qualification of laboratory instruments, coordinates vendor servicing activities, and supports the broader equipment lifecycle from documentation to qualification.

You will participate in investigations, deviations, CAPA, and other quality system activities while