QC Lab Calibration & Compliance Specialist

No-Deviation-Pte.-Ltd; Singapore; On-site; SGD 42,000 - 64,000; Full time

Benefits offered by this job

Generous Leave Policy

Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Shape the Future

Job summary

No deviation in Singapore seeks a QC support professional to assist calibration, maintenance, and qualification of laboratory instruments. You will help maintain documentation integrity, SOPs, and change controls while contributing to investigations, deviations, CAPA, and audit readiness within the QC department.

Ideal candidates hold a science-related diploma/degree, familiarity with GMP, and proficiency in LIMS/MS Office, with strong attention to detail and coordination skills for vendor

Qualifications

• Diploma or Degree in Science, Chemistry, Biology, Pharmacy, or a related discipline.
• Prior experience in a QC laboratory or GMP-regulated environment preferred.
• Familiarity with laboratory equipment calibration, maintenance, and qualification processes.
• Working knowledge of GMP, Data Integrity, and quality system requirements (change control, deviations, CAPA).
• Strong attention to detail and accuracy in documentation.
• Good organizational and coordination skills, with the ability to liaise with vendors and cross-functional teams.
• Effective written and verbal communication skills.

Responsibilities

• Support routine calibration, maintenance, and qualification activities for laboratory instruments.
• Assist in coordinating equipment servicing and vendor maintenance activities.
• Support equipment lifecycle management activities, including documentation updates and qualification records.

Skills

Attention to detail

Communication skills

Vendor coordination

Education

Diploma/ Degree in Science or related

Tools

LIMS

MS Office

Job description

No deviation in Singapore seeks a QC support professional to assist calibration, maintenance, and qualification of laboratory instruments. You will help maintain documentation integrity, SOPs, and change controls while contributing to investigations, deviations, CAPA, and audit readiness within the QC department.

Ideal candidates hold a science-related diploma/degree, familiarity with GMP, and proficiency in LIMS/MS Office, with strong attention to detail and coordination skills for vendor