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.

REQUIRED QUALIFICATIONS

• Diploma/ Degree in Chemistry, Biochemistry, Pharmaceutical Science, or related field.
• 1 to 3 years of laboratory experience in the pharmaceutical or related industry (fresh graduates with strong technical background may be considered).
• Hands-on experience with analytical techniques (HPLC, GC, FTIR, UV, etc.) preferred.
• Knowledge of GMP, pharmacopeial standards (USP/EP/JP), and regulatory guidelines.

• Perform sampling, testing, and analysis of raw materials (API, excipients, packaging materials) in compliance with USP/EP/JP and internal specifications.
• Conduct chemical and physical testing using techniques such as HPLC, GC, UV/Vis, FTIR, Karl Fischer, titration, and wet chemistry methods.
• Review and interpret analytical results to ensure accuracy and reliability.
• Document all testing activities in compliance with Good Documentation Practices (GDP) and maintain laboratory records in LIMS/ELN systems.
• Support raw material release process by preparing Certificates of Analysis (CoAs) and ensuring timely approval for use in production.
• Ensure compliance with GMP, GDP, safety, and regulatory requirements.