QC Analyst

No deviation; Singapore; On-site; SGD 36,000 - 60,000; 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 is seeking a detail-oriented and safety-conscious individual to join our operations team. The role involves performing GMP-compliant tasks, supporting documentation, housekeeping, and data integrity across the site while following SOPs.

The successful candidate will identify deviations, report safety concerns, and communicate with teams. A diploma or higher in a relevant field is required, with willingness to work shift schedules if needed.

Qualifications

• Diploma or higher in a relevant science, engineering, or related discipline.
• Experience in a GMP-regulated manufacturing environment is preferred.
• Familiarity with SOPs and data integrity practices.
• Strong communication and teamwork skills.
• Willingness to work shift schedules if required.
• Meticulous and safety-conscious; able to follow procedures.

Responsibilities

• Perform assigned operational tasks in accordance with GMP and SOPs
• Identify and report any deviations, non-conformances, or safety concerns in a timely manner
• Support documentation activities such as data entry, document review, and submission of forms
• Assist in routine housekeeping, cleaning, and 6S activities to maintain a compliant and safe work environment
• Participate in training as required for assigned tasks
• Handle materials, components, or equipment as per procedures and safety guidelines
• Uphold data integrity principles in accordance with company policies
• Communicate effectively with team members, supervisors, and cross-functional personnel
• Maintain confidentiality and integrity of company data and operations
• Perform any other tasks as assigned by supervisor

Skills

Communication skills

Teamwork

Attention to detail

Safety-conscious

Education

Diploma or higher in a relevant science, engineering, or related discipline

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.

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 seeking a detail-oriented and safety-conscious individual to join our operations team. The successful candidate will perform assigned operational tasks in compliance with Good Manufacturing Practices (GMP) and standard operating procedures (SOPs), while supporting documentation, housekeeping, and data integrity efforts across the site. This role requires strong attention to detail, a proactive approach to identifying and reporting issues, and effective communication across teams to maintain a safe, compliant, and efficient work environment.

Key Responsibilities

• Perform assigned operational tasks in accordance with GMP and SOPs
• Identify and report any deviations, non-conformances, or safety concerns in a timely manner
• Support documentation activities such as data entry, document review, and submission of forms
• Assist in routine housekeeping, cleaning, and 6S activities to maintain a compliant and safe work environment
• Participate in training as required for assigned tasks
• Handle materials, components, or equipment as per procedures and safety guidelines
• Uphold data integrity principles in accordance with company policies
• Communicate effectively with team members, supervisors, and cross-functional personnel
• Maintain confidentiality and integrity of company data and operations
• Perform any other tasks as assigned by supervisor

Required Qualifications

• Diploma or higher in a relevant science, engineering, or related discipline
• Prior experience in a GMP-regulated manufacturing environment preferred
• Familiarity with SOPs, documentation practices, and data integrity principles
• Good communication and teamwork skills
• Willingness to work shift schedules, if required
• Meticulous, safety-conscious, and able to follow procedures accurately

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.