We're looking for a QC Analyst Grade II to perform routine analytical testing and support QC operations across Technical Services, Incoming Materials, and Finished Products. You'll work independently, follow GMP and SOP requirements, and ensure high‑quality analytical output.
Key Responsibilities
Perform routine analytical testing as assigned by the QC Supervisor or QC Lead Analyst.
Support drafting, checking, and verifying SOPs and specifications.
Ensure full compliance with analytical standards, methods, sampling processes, and training requirements.
Coordinate workload with QC Lead Analyst to meet deadlines.
Peer‑review documentation for QC Analysts where required.
Report issues related to protocols, specifications, equipment validity, or reference materials.
Maintain strong data integrity and good documentation practices.
Perform EHS tasks (waste disposal, glassware cleaning) and ensure QC Analysts I follow EHS requirements.
Demonstrate capability with HPLC, KF titration, dissolution testing, and physical testing of tablets, capsules, and packaging.
Prepare and check analytical data before submitting for review.
Implement corrective actions identified by reviewers.
Maintain accurate analytical documentation and training records.
Carry out equipment care, minor maintenance, and reference standard management as required.
About You
Certificate, Diploma, or BSc in Chemistry, Analytical Sciences, Medical Lab Science, or equivalent experience.
Strong analytical background with substantial QC lab experience.
Experience with HPLC and method troubleshooting (Agilent/OpenLab preferred).
Skilled in a broad range of analytical techniques.
Strong attention to detail with clear communication skills.
Proficient in Microsoft Office and comfortable working independently