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 dedicated QC Chemist to join our Client’s Quality Control team on a contract basis. This role is part of a permanent night shift team supporting routine testing of in-process samples and finished pharmaceutical products. The ideal candidate must have hands-on experience in High-Performance Liquid Chromatography (HPLC) and other analytical techniques, and a solid understanding of GMP requirements in a regulated environment.

REQUIRED QUALIFICATIONS

• Diploma or Bachelors degree in Chemistry, Pharmaceutical Science, or a related field.
• Minimum 2 years of hands-on experience with HPLC in a pharmaceutical QC lab.
• Familiarity with GMP and regulatory guidelines (e.g., USP, EP, ICH).
• Ability to work independently during night shift with minimal supervision.
• Strong attention to detail and good documentation practices.
• Good communication and teamwork skills.
• Comfortable working in a fast-paced and dynamic environment.

• Perform analytical testing using HPLC, UV-Vis spectrophotometry, FTIR, KF titration, and other QC techniques in accordance with SOPs and test methods.
• Review and interpret analytical results to ensure accuracy, reliability, and compliance.
• Ensure all testing is conducted in compliance with GMP, GLP, and safety protocols.
• Document test results clearly and accurately in logbooks, LIMS, and other systems.
• Participate in routine equipment calibration, maintenance, and troubleshooting.
• Support investigation of non-conformances, deviations, and out-of-specification (OOS) results.
• Assist in preparation of reagents, reference standards, and stability samples as required.
• Maintain a clean, safe, and compliant laboratory environment at all times.
• Collaborate with cross-functional teams to ensure timely testing and release of products.