QC Lab Calibration & Compliance Specialist

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 42,000 - 66,000; Full time

Benefits offered by this job

Leave policy

Health & wellness coverage

Professional development

Inclusive culture

Industry impact

Job summary

No deviation Pte. Ltd. in Singapore seeks a QC Laboratory Support professional to maintain equipment reliability, ensure documentation integrity, and uphold GMP standards.

You will assist with calibration, maintenance, qualification, and change controls while contributing to CAPA, deviations, and audit readiness. Collaboration with vendors and cross-functional teams is essential. The role emphasizes laboratory best practices, SOP updates, and continuous improvement within the QC department to

Qualifications

• Diploma or degree in science, chemistry, biology, pharmacy or related discipline.
• Strong attention to detail and accuracy in documentation.
• Effective written and verbal communication; good organizational and coordination 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; update qualification records and documentation.
• Ensure laboratory documentation is completed accurately and timely.
• Assist in preparing and revising SOPs, forms, and records.
• Raise and coordinate Change Controls for equipment, docs, and process improvements per GMP.
• Support investigations, deviations, CAPA, and other quality system activities.
• Comply with GMP, data integrity, EHS, and quality requirements.
• Participate in laboratory audits and inspection readiness activities.
• Support process improvement and implementation of best practices in QC.

Education

Diploma or Degree in Science, Chemistry, Biology, Pharmacy, or related discipline

Tools

LIMS

MS Office

Job description

No deviation Pte. Ltd. in Singapore seeks a QC Laboratory Support professional to maintain equipment reliability, ensure documentation integrity, and uphold GMP standards.

You will assist with calibration, maintenance, qualification, and change controls while contributing to CAPA, deviations, and audit readiness. Collaboration with vendors and cross-functional teams is essential. The role emphasizes laboratory best practices, SOP updates, and continuous improvement within the QC department to