Quality Control Officer

As a Quality Control Analyst, you will be responsible for conducting routine and specialized analytical testing on Solid Oral Dosage Forms, including Finished Products, Raw Materials, In-Process Samples, and Stability Samples. Your key responsibilities will include: - Performing and documenting Analytical Method Validation in accordance with regulatory guidelines. - Supporting Process and Product Quality Assurance (PMQC) activities through data review and root cause analysis. - Executing dissolution testing and ensuring accuracy, precision, and compliance with established protocols. - Maintaining and troubleshooting analytical instruments to ensure optimal performance and data reliability. - Preparing and reviewing technical reports, batch records, and regulatory documentation. - Collaborating with cross-functional teams to resolve quality issues and support continuous improvement initiatives. Qualifications required for this role include: - B.Sc./ M.Sc./ B. Pharm/ M.Pharm degree. - 2 to 8 years of experience in the analysis of Solid Oral - FP, RM, In-process, or Stability. - Experience in Analytical Method Validation. - Experience in PMQC & Dissolution. If you are interested in this position, the interview is scheduled at 09:00 AM to 04:00 PM at Hotel Silver Leaf, Plot No-CM-14 & 15, Raghuvir Complex, Opp. Vapi Industries. As a Quality Control Analyst, you will be responsible for conducting routine and specialized analytical testing on Solid Oral Dosage Forms, including Finished Products, Raw Materials, In-Process Samples, and Stability Samples. Your key responsibilities will include: - Performing and documenting Analytical Method Validation in accordance with regulatory guidelines. - Supporting Process and Product Quality Assurance (PMQC) activities through data review and root cause analysis. - Executing dissolution testing and ensuring accuracy, precision, and compliance with established protocols. - Maintaining and troubleshooting analytical instruments to ensure optimal performance and data reliability. - Preparing and reviewing technical reports, batch records, and regulatory documentation. - Collaborating with cross-functional teams to resolve quality issues and support continuous improvement initiatives. Qualifications required for this role include: - B.Sc./ M.Sc./ B. Pharm/ M.Pharm degree. - 2 to 8 years of experience in the analysis of Solid Oral - FP, RM, In-process, or Stability. - Experience in Analytical Method Validation. - Experience in PMQC & Dissolution. If you are interested in this position, the interview is scheduled at 09:00 AM to 04:00 PM at Hotel Silver Leaf, Plot No-CM-14 & 15, Raghuvir Complex, Opp. Vapi Industries.