QC Analytical Support Officer

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 33,000 - 42,000; Full time

Benefits offered by this job

Leave policy

Health & dental coverage

Professional development opportunities

Inclusive culture

Career growth

Job summary

No deviation is seeking a QC Laboratory Associate to join the Quality Control department at GSK Jurong. This role oversees day-to-day equipment management, ensures GMP-compliant documentation, and supports data integrity, CAPA, and change control in a global pharma setting.

Early-career candidates are encouraged to apply. The successful candidate will work in a regulated laboratory environment, contributing to continuous improvement initiatives and audits while developing a strong foundation in

Qualifications

• 0-2 years in a laboratory or QC environment; fresh graduates encouraged to apply.
• Basic understanding of GMP and laboratory quality/documentation practices preferred.
• Good attention to detail and strong documentation habits.
• Ability to work well in a regulated laboratory environment with structured procedures.
• Willingness to learn and adapt in a GMP setting.

Responsibilities

• Equipment Management: support routine calibration, maintenance, and qualification activities for laboratory instruments.
• Documentation and Compliance: ensure documentation is completed accurately and SOPs/records are prepared and updated; assist in investigations, deviations, CAPA and change control.
• Continuous Improvement: participate in laboratory audits and inspection readiness; support process improvements and best practices in QC.

Skills

Attention to detail

Documentation

Teamwork

Willingness to learn

Education

Bachelor's degree in Chemistry, Biotechnology, Life Sciences, Pharmaceutical Science, or related field

Job description

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation. We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development - empowering our team members to grow personally and professionally.

Position Overview

We are looking for a QC Laboratory Associate to join the Quality Control department at GSK Jurong. This role supports the day-to-day management of laboratory equipment, ensures documentation meets GMP and data integrity standards, and contributes to continuous improvement initiatives within the lab. It's a great opportunity for early-career candidates - including fresh graduates - looking to build a strong foundation in pharmaceutical quality control within a global organization.

Key Responsibilities

• Equipment Management
  • Support routine calibration, maintenance, and qualification activities for laboratory instruments.
  • Maintain equipment logbooks and associated documentation.
  • Assist in coordinating equipment servicing and vendor maintenance activities.
• Documentation and Compliance
  • Ensure laboratory documentation is completed accurately and in a timely manner.
  • Assist in the preparation and revision of Standard Operating Procedures (SOPs), forms, and laboratory records.
  • Support investigations, deviations, CAPA, and change control activities when required.
  • Comply with GMP, data integrity, EHS, and company quality requirements.
• Continuous Improvement
  • Participate in laboratory audits and inspection readiness activities.
  • Support process improvement initiatives within the QC department.
  • Assist in implementation of laboratory best practices and operational excellence initiatives.

Required Qualifications

• Degree in Chemistry, Biotechnology, Life Sciences, Pharmaceutical Science, or a related field.
• 0-2 years of relevant experience in a laboratory or QC environment - fresh graduates are encouraged to apply.
• Basic understanding of GMP and laboratory quality/documentation practices preferred.
• Good attention to detail and strong documentation habits.
• Ability to work well in a team and follow structured procedures.
• Willingness to learn and adapt in a regulated laboratory environment.

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.