Key Responsibilities:

- Perform quantitative and qualitative testing on pharmaceutical materials

- Analyze results against established specifications and document findings

- Investigate OOS results through root cause analysis

- Calibrate, maintain, and troubleshoot analytical instruments

- Prepare methods,

validation protocols, and cGMP reports

Requirements:

- Bachelor's or Master's degree in Chemistry, Pharmacy, or related science

- Minimum seven years' pharmaceutical Quality Control Analyst experience

- Hands-on experience with HPLC, GC, spectrophotometers, and dissolution testers

- Solid GMP and pharmaceutical regulatory knowledge

- Proficiency in analytical method development and validation

Apply pharmaceutical analysis, HPLC expertise, GMP knowledge, and meticulous documentation skills as a Senior Quality Control Analyst