QC Specialist

No deviation Pte Ltd.; Singapore; Hybrid; SGD 56,000 - 89,000; Full time

Benefits offered by this job

Generous leave

Health coverage

Professional development

Inclusive culture

Career growth

Job summary

No deviation Pte Ltd. is seeking QC Personnel to support daily quality control activities in a GMP environment in Singapore. You will perform routine testing, document results, and assist in method validation and investigations.

Join a collaborative team focusing on quality, regulatory readiness, and continuous improvement across QA, Manufacturing, and MSAT functions.

Qualifications

• Diploma or degree in Chemistry, Pharmaceutical Science, Biotechnology, Microbiology, Life Sciences, or related discipline.
• Minimum 2 to 5 years of QC laboratory experience in GMP-regulated environments.
• Experience with method validation, verification, or transfer.
• Hands-on experience with GLIMS, Veeva, and SAP.
• Familiar with GMP, GDP, data integrity, ALCOA+, and laboratory compliance.

Responsibilities

• Perform routine QC testing for materials and finished products.
• Execute laboratory testing in accordance with SOPs and GMP requirements.
• Ensure data integrity and timely documentation of activities.
• Support method validation, verification, transfer, and qualification activities.
• Maintain ALCOA+-compliant documentation and support investigations.

Skills

QC testing

Data integrity

ALCOA+

Documentation

Education

Diploma or Degree in Chemistry, Pharmaceutical Science, Biotechnology, Microbiology, Life Sciences, or related discipline

Tools

GLIMS

Veeva

SAP

HPLC

GC

UV

Job description

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

The QC Personnel will be responsible for supporting day‑to‑day Quality Control laboratory activities, including testing, documentation, method validation support, data review, and compliance with GMP requirements. The role requires hands‑on experience with laboratory systems such as GLIMS, Veeva, and SAP, as well as experience in analytical method validation activities.

Key Responsibilities

• Perform routine QC testing for raw materials, intermediates, finished products, stability samples, and/or environmental monitoring samples, as applicable
• Execute laboratory testing in accordance with approved SOPs, test methods, specifications, and GMP requirements.
• Ensure all laboratory activities are completed accurately, timely, and in compliance with data integrity expectations.
• Support sample receipt, testing coordination, result entry, and laboratory documentation.
• Support analytical method validation, verification, transfer, and qualification activities.
• Execute validation protocols and document results in accordance with approved acceptance criteria.
• Assist in the preparation, review, and closure of method validation protocols, reports, deviations, and supporting documentation.
• Support troubleshooting of analytical methods and laboratory investigations where required.
• Use GLIMS for sample management, test assignment, result entry, and laboratory workflow tracking.
• Use Veeva for document management, SOP retrieval, document review, training, and quality records where applicable.
• Use SAP for material/sample-related transactions, inventory checks, batch information retrieval, or quality-related processes.
• Ensure proper documentation practices in line with ALCOA+ principles and GMP expectations.
• Support laboratory investigations, OOS/OOT investigations, deviations, CAPA, and change control activities.
• Ensure timely escalation of abnormal results, laboratory issues, equipment issues, or documentation discrepancies.
• Participate in internal audits, external inspections, and laboratory readiness activities.
• Maintain laboratory areas, equipment, reagents, standards, and records in an inspection‑ready state
• Support calibration, maintenance, and qualification readiness of laboratory equipment.
• Assist in laboratory process improvements, system updates, and workflow optimization.
• Work closely with QA, Manufacturing, MSAT, Validation, and Supply Chain teams to support product release and compliance requirements.

Required Qualifications

• Diploma or Degree in Chemistry, Pharmaceutical Science, Biotechnology, Microbiology, Life Sciences, or related discipline.
• Minimum 2 to 5 years of QC laboratory experience in a pharmaceutical, biologics, medical device, or GMP-regulated environment.
• Experience with method validation, method verification, or method transfer is required.
• Hands‑on experience with laboratory or quality systems such as GLIMS, Veeva, and SAP.
• Experience in QC testing, laboratory documentation, investigations, and GMP compliance.
• Familiar with GMP, GDP, data integrity, ALCOA+, and laboratory compliance requirements.
• Experience with analytical techniques such as HPLC, GC, UV, pH, conductivity, TOC, endotoxin, bioburden, sterility, or other QC methods will be advantageous.
• Able to execute and document method validation activities according to approved protocols.
• Comfortable working with electronic systems for sample tracking, document control, training, and material/batch-related transactions.
• 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.