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QC Raw Material Analyst

3 weeks ago

Singapore No deviation Full time

Overview
QC Raw Material Analyst (6 months Contract) – Join to apply for the QC Raw Material Analyst (6 months Contract) role at No deviation.
This range is provided by No deviation. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
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 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.
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.
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.
Seniority level
Entry level
Employment type
Contract
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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