1,260 Quality Control Analyst jobs in India

This role is for one of Weekday’s clients
Salary range: Rs - Rs (ie INR 2-7 LPA)
Min Experience: 2 years
Location: Hyderabad
JobType: full-time

Requirements

We are seeking a motivated Quality Control Analyst with 2-7 years of experience specializing in HPLC, GC, and wet chemical analysis to join our botanical healthcare manufacturing operations. The ideal candidate will ensure that raw materials, in-process samples, and finished products meet quality standards as per regulatory and company guidelines. The role involves hands-on testing, data interpretation, and reporting for botanical and herbal healthcare products.

• Perform routine and non-routine analysis of raw materials, intermediates, and finished products using HPLC, GC, and wet chemical methods.
• Ensure compliance with standard operating procedures (SOPs), Good Manufacturing Practices (GMP), and regulatory requirements.
• Prepare and maintain accurate analytical records, test results, and reports.
• Conduct method validation and troubleshooting of analytical instruments as needed.
• Collaborate with R&D and production teams to ensure quality standards during product development and manufacturing.
• Monitor and maintain laboratory equipment, ensuring calibration and maintenance schedules are followed.
• Participate in internal and external audits and assist in implementing corrective actions.
• Maintain cleanliness and safety standards in the QC laboratory.
• Support stability studies and other quality-related projects.

• Bachelor’s degree in Chemistry, Pharmacy, Life Sciences, or a related field.
• 2-7 years of experience in quality control, preferably in the botanical or herbal healthcare industry.
• Hands-on experience with HPLC, GC, and wet chemical analysis.
• Good understanding of GMP and quality standards.
• Ability to interpret chromatograms and analytical data accurately.
• Strong attention to detail and problem-solving skills.
• Good communication and teamwork abilities.

• Experience working in manufacturing or factory environments.
• Knowledge of regulatory requirements applicable to botanical healthcare products.
• Experience with documentation and data management software

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis spectroscopy, and dissolution testing.
• Accurately document all testing procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Prepare reagents, solutions, and standards required for analytical testing.
• Calibrate and maintain laboratory equipment to ensure accuracy and reliability of test results.
• Review and interpret analytical data, identifying any deviations from specifications and escalating them to the Quality Control Supervisor.
• Participate in method validation and transfer activities for new analytical methods.
• Contribute to the investigation of out-of-specification (OOS) results and implementation of corrective and preventive actions (CAPAs).
• Ensure a safe working environment by adhering to all laboratory safety protocols and procedures.
• Collaborate with R&D, Production, and Quality Assurance departments to resolve quality-related issues.
• Stay up-to-date with current pharmacopoeial standards and regulatory guidelines.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field.
• Minimum of 3 years of experience in a pharmaceutical quality control laboratory.
• Proficiency in common analytical techniques and instrumentation used in pharmaceutical testing.
• Familiarity with GMP and GLP requirements.
• Strong attention to detail and accuracy in data recording and reporting.
• Excellent problem-solving and critical thinking skills.
• Good written and verbal communication skills.
• Ability to work effectively both independently and as part of a team in a hybrid work environment.

• Perform analytical tests on raw materials, intermediates, and finished pharmaceutical products using various instruments (e.g., HPLC, GC, UV-Vis Spectrophotometer).
• Prepare and standardize reagents and solutions.
• Document all testing procedures, results, and deviations in accordance with SOPs.
• Calibrate and maintain laboratory equipment.
• Review and analyze test data, and prepare quality control reports.
• Ensure compliance with all relevant regulatory requirements (e.g., GMP, FDA).
• Investigate out-of-specification (OOS) results and deviations.
• Participate in method validation and transfer activities.
• Maintain a clean and organized laboratory environment.
• Contribute to continuous improvement initiatives within the Quality Control department.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a related discipline.
• Minimum of 3 years of experience in pharmaceutical quality control or quality assurance.
• Hands-on experience with analytical instruments like HPLC, GC, FTIR, UV-Vis.
• Strong knowledge of pharmaceutical analytical methods and validation.
• Familiarity with GMP, ICH guidelines, and other regulatory requirements.
• Excellent attention to detail and accuracy in data recording.
• Good laboratory practices (GLP) knowledge.
• Strong problem-solving and analytical skills.
• Effective written and verbal communication skills.

• Perform analytical tests on raw materials, intermediates, and finished products.
• Utilize various laboratory instruments such as HPLC, GC, UV-Vis, and dissolution testers.
• Ensure compliance with GLP, GMP, and other regulatory guidelines.
• Maintain accurate and detailed laboratory records and test results.
• Prepare Certificates of Analysis (CoA) for released products.
• Participate in method validation and instrument calibration activities.
• Troubleshoot laboratory equipment and analytical methods.
• Collaborate with cross-functional teams on quality-related issues.
• Contribute to continuous improvement of QC processes.
• Adhere to safety protocols in the laboratory.

• Bachelor's or Master's degree in Pharmacy, Chemistry, or a related science field.
• Proven experience as a Quality Control Analyst in the pharmaceutical industry.
• Hands-on experience with analytical techniques and laboratory instrumentation.
• Knowledge of pharmacopoeial standards (IP, USP, BP).
• Familiarity with GLP and GMP requirements.
• Strong analytical, problem-solving, and record-keeping skills.
• Excellent attention to detail and organizational abilities.
• Ability to work effectively in a team environment.

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
• Utilize various analytical instruments and techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Document all laboratory procedures, results, and observations accurately.
• Analyze test data, interpret results, and prepare detailed quality control reports.
• Ensure compliance with GLP, GMP, and relevant regulatory guidelines.
• Participate in method validation, transfer, and verification activities.
• Maintain laboratory equipment, including calibration and qualification.
• Investigate out-of-specification (OOS) results and deviations, implementing CAPAs.
• Collaborate with QA, R&D, and Production departments on quality-related matters.
• Assist in the training and development of junior QC analysts.

• Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline.
• Minimum of 5 years of experience in pharmaceutical quality control analysis.
• Hands-on experience with analytical instrumentation such as HPLC, GC, and spectrophotometers.
• Thorough understanding of GMP, GLP, and pharmaceutical regulatory requirements.
• Proficiency in data analysis and report writing.
• Strong problem-solving and troubleshooting skills.
• Excellent attention to detail and organizational abilities.
• Good written and verbal communication skills.
• Ability to work independently and as part of a team.

• Perform routine quality control tests on raw materials, in-process samples, and finished products using established analytical methods (e.g., HPLC, GC, UV-Vis spectrophotometry).
• Calibrate and maintain laboratory equipment.
• Document all testing procedures, results, and observations accurately and according to SOPs.
• Analyze and interpret test data, identify any deviations from specifications, and report them to supervisors.
• Assist in the investigation of out-of-specification (OOS) results.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other regulatory requirements.
• Prepare reports on quality control testing and product release.
• Participate in method validation and transfer activities.
• Maintain laboratory cleanliness and safety standards.
• Stay updated with industry advancements and regulatory changes in pharmaceutical quality control.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related science field.
• Minimum of 2 years of experience in pharmaceutical quality control or a related laboratory setting.
• Hands-on experience with analytical instruments such as HPLC, GC, FTIR, and dissolution testers.
• Strong understanding of pharmaceutical quality systems and regulatory guidelines (e.g., ICH, FDA).
• Proficiency in data analysis and interpretation.
• Excellent attention to detail and accuracy.
• Good written and verbal communication skills.
• Ability to work effectively both independently and as part of a team.