QC Raw Material Analyst

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 64,000 - 91,000; Full time

Job summary

A dynamic engineering consultancy in Singapore seeks a QC Raw Material Analyst to sample, test, and release incoming raw materials. The candidate will ensure compliance with GMP standards and safeguard product quality. A degree in Chemistry or Biological Chemistry and relevant handling experience are required. The role offers a generous leave policy and comprehensive health coverage.

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Career advancement opportunities

Qualifications

• Relevant work experience preferably with Raw Material handling.
• Understanding of compendial monographs and the chemistry fundamentals behind methods.
• Experience with compendial testing listed in the USP, JP and EP monographs.

Responsibilities

• Perform testing and analysis of raw materials and final products.
• Document and ensure data integrity and compliance with GMP.
• Manage sample logistics and participate in method transfers.

Skills

Analytical testing

Data integrity

GMP compliance

Chemical handling

Education

Degree in Chemistry or Biological Chemistry

Tools

HPLC

UV Spectroscopy

Infrared Spectroscopy

pH Meter

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

The QC Raw Material Analyst is responsible for sampling, testing, and releasing incoming raw materials in accordance with GMP, pharmacopeial standards, and company procedures. The role ensures that only materials meeting defined specifications are used in manufacturing, thereby safeguarding product quality and patient safety.

Key Responsibilities

• Perform testing and analysis of raw materials, in-process, and final products, as well as environmental samples, following SOPs, Test Methods, and cGMP standards.
• Document, review, and ensure data integrity and compliance with GMP requirements.
• Support laboratory operations, including equipment maintenance, housekeeping, inventory control, and preparation of standards and reagents.
• Manage sample logistics, such as retention storage, external lab coordination, document control, and sample shipments.
• Participate in method transfers, validations, and equipment qualification activities.
• Troubleshoot analytical methods, equipment issues, and support OOS or deviation investigations.
• Contribute to continuous improvement and operational efficiency initiatives as assigned by the Manager.

Required Qualifications

• Degree in Chemistry or Biological Chemistry.
• Relevant work experience preferably with Raw Material handling
• Understanding and execution of compendial monographs and the chemistry fundamentals behind methods. Technology/equipment, UV, Infrared Spectroscopy, Osmolality, HPLC, pH, Conductivity, Polarimetry, Refractometry, Density meter, Titration (manual and automatic), as well as all compendial testing listed in the USP, JP and EP monographs.

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.