112 Quality Assurance Analyst jobs in Vadodara

Qualifications and Skills

• Proven experience in a quality control or inspection role for at least 1 year, up to a maximum of 3 years.
• In-depth knowledge of ISO 9001 standards to ensure company meets international quality requisites.
• Proficiency in Six Sigma methodologies to improve processes and reduce defects effectively.
• Familiarity with Non-Destructive Testing (NDT) techniques to evaluate the integrity of materials without causing damage.
• Expertise in Statistical Process Control (SPC) to monitor and control processes through statistical data analysis.
• Skilled in conducting Root Cause Analysis to identify the underlying causes of defects and implement preventive measures.
• Ability to perform Gage R&R Studies to assess the variability in measurement systems for accuracy improvements.
• Experience using Control Charts for tracking process performance and detecting any deviations from standards.
• Competent in using precision measuring tools such as calipers and micrometers for dimensional measurements.

Roles and Responsibilities

• Conduct regular inspections and tests on materials and products to ensure adherence to quality standards.
• Document inspection outcomes by completing detailed reports and production records.
• Identify areas of improvement within the production process and propose solutions to enhance quality.
• Collaborate with production teams to resolve quality issues and implement corrective actions.
• Ensure all quality inspections are performed in compliance with company and regulatory guidelines.
• Assist in the development and implementation of quality control procedures and policies.
• Train and guide manufacturing staff on quality standards and operating procedures.
• Monitor the use of all equipment to ensure they are maintained to quality standards.

• Perform chemical and physical tests on raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis, Titration).
• Calibrate and maintain laboratory equipment to ensure accurate and reliable results.
• Analyze and interpret test data, comparing results against established specifications.
• Document all testing procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Prepare standard solutions and reagents.
• Investigate out-of-specification (OOS) results and deviations, collaborating with relevant departments to identify root causes and implement corrective actions.
• Participate in method validation and transfer activities.
• Maintain a clean and organized laboratory environment.
• Prepare reports summarizing test results and quality control status.
• Ensure compliance with all relevant regulatory guidelines (e.g., FDA, WHO).

• Diploma or Bachelor's degree in Engineering or a related technical field.
• Minimum of 3-5 years of experience in quality control, specifically within the aerospace or aviation industry.
• Proficiency with various inspection tools and techniques (e.g., calipers, micrometers, CMM).
• Strong understanding of aerospace quality standards (e.g., AS9100).
• Ability to read and interpret complex engineering drawings and specifications.
• Excellent attention to detail and accuracy.
• Good written and verbal communication skills.
• Ability to work independently and as part of a team.

• Develop and implement robust quality control plans and procedures for all manufacturing processes.
• Conduct regular inspections and audits of raw materials, in-process materials, and finished goods.
• Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA) to address non-conformities.
• Lead root cause analysis investigations for quality issues and drive effective solutions.
• Collaborate with production teams to ensure adherence to quality standards and specifications.
• Develop and deliver quality training programs for manufacturing personnel.
• Manage the calibration and maintenance of quality control equipment and instrumentation.
• Stay updated with industry quality standards (e.g., ISO 9001) and regulatory requirements.
• Contribute to the continuous improvement of quality management systems (QMS).
• Interface with suppliers regarding material quality and performance.
• Prepare detailed quality reports for management review.
• Champion a quality-first culture throughout the organization.

• Bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related technical field.
• Minimum 6 years of experience in quality control or quality assurance within a manufacturing environment.
• In-depth knowledge of quality control methodologies, statistical process control (SPC), and problem-solving techniques.
• Experience with ISO 9001 or other relevant quality management systems.
• Proficiency in using quality control tools and equipment.
• Strong analytical and data interpretation skills.
• Excellent communication, leadership, and interpersonal skills.
• Ability to work collaboratively across different departments.
• Experience in the manufacturing industry is mandatory.
• Six Sigma Green Belt or Black Belt certification is a strong advantage.

Responsibilities

• Lead and manage the Quality Control team, ensuring effective allocation of responsibilities, mentoring, and performance monitoring.
• Establish, implement, and continually improve QC systems aligned with ISO 9001:2015 and other relevant quality standards.
• Oversee inspection, testing, and certification processes across all production stages to ensure full compliance with internal and international customer requirements.
• Drive continuous improvement initiatives in quality systems, measurement techniques, and reporting.
• Ensure accuracy, completeness, and long-term traceability of all quality records and documentation.
• Liaise with internal departments, customers, and external auditors to demonstrate compliance and manage audits effectively.
• Implement advanced quality tools, data analysis, and root-cause investigation methodologies to prevent recurrence of non-conformances.

Qualifications

• Graduate degree in Engineering, Materials Science, or related discipline (postgraduate preferred).
• Minimum 10 years of progressive experience in Quality Control / Quality Assurance, with at least 5 years in a leadership role heading a team.
• Strong familiarity with ISO 9001:2015 standards and audit processes.
• Demonstrated expertise in developing, maintaining, and auditing comprehensive quality documentation systems.
• Proven ability to manage high-complexity projects with demanding compliance and international customer standards.
• Excellent written and verbal communication skills, with a strong focus on accuracy, clarity, and documentation discipline.

Required Skills

• Strong leadership and team-building skills.
• Meticulous attention to detail with the ability to manage large volumes of documentation.
• High integrity, professionalism, and commitment to compliance.
• Analytical problem-solving with focus on preventive action.
• Ability to interface confidently with auditors, international customers, and senior management.

• Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
• Develop, validate, and transfer analytical methods in accordance with regulatory guidelines (ICH, USP, EP).
• Analyze and interpret test results, ensuring compliance with established specifications and standards.
• Troubleshoot and maintain laboratory equipment, ensuring its proper functioning and calibration.
• Prepare detailed analytical reports, Certificates of Analysis (CoA), and other quality documentation.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Participate in internal and external audits, providing necessary documentation and explanations.
• Ensure adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and all relevant safety regulations.
• Train and mentor junior analysts, providing guidance on analytical techniques and laboratory procedures.
• Contribute to the continuous improvement of quality control processes and systems.
• Collaborate with other departments, such as R&D, Production, and Regulatory Affairs, to resolve quality-related issues.
• Maintain accurate and up-to-date laboratory records.
• Stay informed about the latest advancements in pharmaceutical analysis and regulatory requirements.

• Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific field.
• Minimum of 6 years of experience in pharmaceutical quality control, with a strong focus on analytical method development and validation.
• In-depth knowledge of GMP, GLP, ICH guidelines, and pharmacopeial standards (USP, EP, BP).
• Hands-on experience with analytical instruments such as HPLC, GC, LC-MS, GC-MS, FTIR, UV-Vis spectrophotometer.
• Proficiency in data analysis and interpretation, with strong documentation skills.
• Experience in investigating OOS results and implementing CAPAs.
• Excellent problem-solving and critical-thinking abilities.
• Strong communication and interpersonal skills, with the ability to work effectively in a team.
• Detail-oriented with a high degree of accuracy and precision.
• Experience with stability studies is a plus.