QA/QC Executive job in Vadodara

1. Testing & Analysis:   - Perform routine and non-routine testing of raw materials, in-process samples, finished products, and stability samples.    - Use analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, and dissolution testers.   2. Documentation & Compliance:     - Maintain and review QC documentation, including test records, SOPs, and COAs.     - Ensure compliance with cGMP, FDA, WHO, and other regulatory guidelines.   3. Stability Studies:     - Conduct stability testing as per ICH guidelines.     - Monitor and report deviations in stability profiles.   4. Calibration & Maintenance:     - Calibrate and maintain lab equipment regularly.     - Troubleshoot instrument malfunctions and coordinate with maintenance teams.   5. Sampling & Specifications:     - Follow approved specifications and procedures for sampling and testing.     - Report non-conformities and participate in investigations (OOS, OOT, CAPA).   6. Regulatory & Audit Compliance:     - Prepare for internal and external audits (FDA, MHRA, etc.).     - Implement corrective actions based on audit findings.   Qualifications & Skills :  - Education: B.Pharm/M.Pharm/M.Sc in Chemistry, Microbiology, or a related field.  - Experience: 1-5 years in QC in a pharmaceutical company (freshers may be considered for junior roles).  - Technical Skills: HPLC, GC, UV, FTIR, Microbiological testing, and software like LIMS.  - Knowledge: cGMP, GLP, ICH guidelines, pharmacopeial standards (USP, BP, IP).  - Soft Skills: Attention to detail, teamwork, problem-solving, and communication skills.  1. Testing & Analysis:     - Perform routine and non-routine testing of raw materials, in-process samples, finished products, and stability samples.     - Use analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, and dissolution testers.   2. Documentation & Compliance:     - Maintain and review QC documentation, including test records, SOPs, and COAs.     - Ensure compliance with cGMP, FDA, WHO, and other regulatory guidelines.   3. Stability Studies:     - Conduct stability testing as per ICH guidelines.     - Monitor and report deviations in stability profiles.   4. Calibration & Maintenance:     - Calibrate and maintain lab equipment regularly.     - Troubleshoot instrument malfunctions and coordinate with maintenance teams.   5. Sampling & Specifications:     - Follow approved specifications and procedures for sampling and testing.     - Report non-conformities and participate in investigations (OOS, OOT, CAPA).   6. Regulatory & Audit Compliance:     - Prepare for internal and external audits (FDA, MHRA, etc.).     - Implement corrective actions based on audit findings.    Qualifications & Skills:  - Education: B.Pharm/M.Pharm/M.Sc in Chemistry, Microbiology, or a related field.  - Experience: 1-5 years in QC in a pharmaceutical company (freshers may be considered for junior roles).  - Technical Skills: HPLC, GC, UV, FTIR, Microbiological testing, and software like LIMS.  - Knowledge: cGMP, GLP, ICH guidelines, pharmacopeial standards (USP, BP, IP).  - Soft Skills: Attention to detail, teamwork, problem-solving, and communication skills.