19 Diamond Processing jobs in Surat

• Developing and validating new testing methodologies and equipment calibration procedures.
• Analyzing production data to identify trends, root causes of defects, and implement corrective and preventative actions (CAPA).
• Collaborating closely with R&D, production, and engineering teams to address quality issues and contribute to product development cycles.
• Ensuring compliance with relevant industry standards, regulatory requirements, and internal quality policies.
• Preparing comprehensive quality reports, performance metrics, and trend analyses for management review.
• Mentoring and training junior quality control technicians, fostering a culture of continuous improvement and excellence.
• Maintaining accurate and organized records of all quality-related activities and documentation.
• Conducting internal audits to assess adherence to quality standards and identify potential non-conformities.
• Staying abreast of the latest advancements in quality control technologies and manufacturing best practices.
• Contributing to the overall strategic direction of the quality management system.

• Develop, implement, and refine quality control procedures and standards for textile production.
• Conduct comprehensive inspections of raw materials, in-process materials, and finished goods.
• Utilize various measurement and testing equipment to assess product specifications and performance.
• Identify non-conforming products and defective materials, documenting findings accurately.
• Analyze quality data to identify trends, root causes of defects, and areas for improvement.
• Collaborate with production supervisors and manufacturing engineers to implement corrective and preventive actions.
• Train and mentor junior quality control staff on inspection techniques and quality standards.
• Ensure compliance with industry regulations, customer specifications, and internal quality policies.
• Maintain detailed records of inspection results, quality metrics, and improvement initiatives.
• Participate in internal and external audits to verify adherence to quality management systems.
• Contribute to continuous improvement efforts by recommending process enhancements and quality initiatives.
• Conduct visual inspections for aesthetic defects, color consistency, and dimensional accuracy.
• Perform functional tests to ensure product performance meets established criteria.
• Work closely with the R&D department on new product quality assessments.
• Oversee the calibration and maintenance of all quality control testing equipment.

• Bachelor's degree in Textile Engineering, Manufacturing Technology, or a related field.
• A minimum of 7 years of experience in quality control within the textile manufacturing industry.
• In-depth knowledge of textile production processes, materials, and common defects.
• Proficiency in using quality inspection tools and measurement equipment.
• Strong understanding of quality management systems (e.g., ISO 9001).
• Excellent analytical, problem-solving, and decision-making skills.
• Detail-oriented with a high level of accuracy.
• Effective communication and interpersonal skills for cross-functional collaboration.
• Ability to interpret technical drawings and specifications.
• Experience in training and leading a team is a plus.
• Familiarity with statistical process control (SPC) techniques is advantageous.

• Develop and implement comprehensive quality control plans and procedures for manufacturing processes.
• Conduct regular inspections and tests on raw materials, in-process materials, and finished products to ensure compliance with specifications.
• Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA) to address non-conformities.
• Lead and participate in internal and external audits to ensure compliance with quality standards (e.g., ISO 9001).
• Collaborate with production, engineering, and R&D teams to resolve quality issues and improve product design.
• Train and mentor junior quality control technicians and inspectors.
• Maintain accurate and detailed quality records, including test results, inspection reports, and deviation reports.
• Develop and manage quality control documentation, including SOPs, work instructions, and specifications.
• Oversee the calibration and maintenance of quality control equipment and instrumentation.
• Stay informed about industry best practices, new technologies, and regulatory requirements related to quality control.
• Drive a culture of quality throughout the organization, promoting awareness and accountability.
• Contribute to continuous improvement initiatives aimed at enhancing product quality, process efficiency, and customer satisfaction.
• Manage supplier quality, including audits and performance evaluations.

• Bachelor's degree in Engineering (Mechanical, Industrial, Chemical, or related field).
• Minimum of 6 years of experience in quality control or quality assurance within a manufacturing environment.
• Strong understanding of quality management systems (QMS), such as ISO 9001.
• Proficiency in statistical process control (SPC) techniques and quality tools (e.g., Six Sigma, Lean Manufacturing).
• Experience with various inspection and testing methods and equipment.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong leadership, communication, and interpersonal skills.
• Ability to read and interpret technical drawings, specifications, and standards.
• Experience in the manufacturing sector relevant to our client's operations is highly preferred.
• Proficiency in using quality management software.
• Certification like ASQ Certified Quality Engineer (CQE) is a plus.

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.

• Conduct comprehensive analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and implement new analytical methods according to regulatory guidelines (e.g., ICH, USP, BP).
• Analyze test results, interpret data, and generate detailed reports, ensuring accuracy and compliance.
• Investigate deviations, out-of-specification (OOS) results, and critical quality issues, proposing and implementing corrective and preventive actions (CAPAs).
• Maintain laboratory equipment, ensuring it is calibrated, qualified, and in good working order.
• Ensure adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) at all times.
• Contribute to the continuous improvement of quality control processes and laboratory operations.
• Prepare and review Standard Operating Procedures (SOPs) and other quality-related documents.
• Train and mentor junior analysts, providing guidance on testing procedures and analytical techniques.
• Collaborate with R&D, Production, and Regulatory Affairs departments to resolve quality-related issues.

• Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
• Extensive hands-on experience with analytical instrumentation such as HPLC, GC, spectroscopy, and dissolution apparatus.
• Thorough understanding of cGMP, GLP, and relevant regulatory guidelines (ICH, USP, BP, EP).
• Proven ability to develop and validate analytical methods.
• Strong data analysis and interpretation skills, with meticulous attention to detail.
• Excellent written and verbal communication skills.
• Experience with laboratory information management systems (LIMS) is a plus.
• Ability to work effectively in a team-oriented environment, with a hybrid work arrangement.

• Perform a variety of chemical and physical tests on raw materials, intermediates, and finished pharmaceutical products.
• Operate and maintain analytical instruments including HPLC, GC, UV-Vis, IR, and dissolution apparatus.
• Conduct method validation studies according to ICH guidelines.
• Analyze and interpret test results, documenting findings accurately and comprehensively.
• Prepare Certificates of Analysis (CoA) and other quality control documentation.
• Ensure compliance with Good Manufacturing Practices (GMP) and other regulatory standards.
• Troubleshoot analytical methods and instrumentation issues.
• Participate in Out-of-Specification (OOS) investigations and contribute to Corrective and Preventive Actions (CAPA).
• Collaborate with R&D, production, and regulatory affairs teams to address quality-related matters.
• Maintain laboratory records and ensure equipment calibration and qualification.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, Biotechnology, or a related field.
• Minimum of 4-5 years of hands-on experience in pharmaceutical quality control or analytical development.
• Proficiency in using various analytical techniques and instrumentation (HPLC, GC, UV-Vis, etc.).
• Strong understanding of pharmaceutical regulatory guidelines (GMP, ICH).
• Excellent data analysis, interpretation, and reporting skills.
• Meticulous attention to detail and strong record-keeping abilities.
• Good problem-solving skills and ability to troubleshoot effectively.
• Effective communication and teamwork skills.
• Experience with laboratory information management systems (LIMS) is a plus.

• Perform comprehensive analytical testing on pharmaceutical raw materials, intermediates, and finished products using various techniques, including HPLC, GC, UV-Vis, FTIR, and Karl Fischer titration.
• Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH, FDA, EMA).
• Prepare and analyze samples according to approved Standard Operating Procedures (SOPs) and test methods.
• Operate and maintain laboratory equipment, ensuring calibration, qualification, and preventative maintenance are performed as scheduled.
• Accurately record, analyze, and interpret test data, ensuring all results are documented in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Investigate Out-of-Specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Contribute to the preparation and review of analytical documentation, including test reports, method validation protocols, and validation reports.
• Collaborate with R&D, production, and regulatory affairs departments to address product quality issues and support new product development.
• Ensure a safe laboratory environment by adhering to all safety protocols and guidelines.
• Participate in internal and external audits as required, providing necessary documentation and explanations.
• Stay updated on current pharmacopoeial standards and regulatory updates relevant to pharmaceutical quality control.
• Train and mentor junior chemists and technicians on analytical techniques and laboratory procedures.

• Master's degree in Pharmaceutical Chemistry, Analytical Chemistry, Organic Chemistry, or a related field.
• Minimum of 5 years of experience in pharmaceutical quality control, with a strong emphasis on analytical testing and method validation.
• Proven expertise in operating and troubleshooting analytical instrumentation, particularly HPLC and GC systems.
• In-depth knowledge of pharmacopoeias (e.g., USP, EP, IP) and regulatory guidelines (GMP, GLP, ICH).
• Excellent analytical, problem-solving, and documentation skills.
• Strong attention to detail and commitment to accuracy.
• Effective communication and interpersonal skills.
• Ability to work independently and as part of a collaborative team in a laboratory setting.
• Experience with data integrity principles is essential.

• Develop, implement, and maintain comprehensive quality control plans and procedures.
• Supervise and guide the quality control team, ensuring efficient workflow and adherence to protocols.
• Conduct regular inspections and audits of raw materials, in-process materials, and finished goods.
• Utilize statistical methods and tools (e.g., SPC, Six Sigma) to monitor and analyze production quality.
• Identify non-conformance issues, investigate root causes, and implement corrective and preventive actions (CAPA).
• Collaborate with production, engineering, and R&D teams to address quality concerns and improve product design.
• Ensure compliance with relevant industry standards (e.g., ISO 9001) and regulatory requirements.
• Manage the calibration and maintenance of testing and measurement equipment.
• Develop and deliver training programs to production staff on quality standards and procedures.
• Maintain accurate quality records, documentation, and traceability systems.
• Analyze quality data to identify trends and opportunities for process improvement.
• Prepare detailed quality reports for management review.
• Participate in supplier quality audits and assessments.
• Drive continuous improvement initiatives within the quality control department and across the manufacturing floor.
• Champion a quality-focused culture throughout the organization.

• Bachelor's degree in Engineering (Mechanical, Industrial, Chemical, or related field) or equivalent practical experience.
• Minimum of 5 years of experience in quality control or quality assurance within a manufacturing setting.
• Strong understanding of quality management systems (QMS), such as ISO 9001.
• Proficiency in statistical process control (SPC), Six Sigma methodologies, and root cause analysis techniques.
• Experience with various inspection and testing methods and equipment.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong leadership and team management abilities.
• Effective communication and interpersonal skills, with the ability to collaborate across departments.
• Detail-oriented with a commitment to accuracy and precision.
• Experience in the **Surat, Gujarat, IN** manufacturing hub is preferred, as this is a hands-on, on-site role.

• Develop, validate, and transfer analytical methods for drug substance and drug product testing using techniques such as HPLC, GC, spectroscopy (UV-Vis, IR, MS), and dissolution testing.
• Perform routine quality control testing of raw materials, intermediates, and finished pharmaceutical products according to established SOPs and regulatory guidelines.
• Investigate Out-of-Specification (OOS) results, identify root causes, and implement corrective and preventive actions (CAPAs).
• Write, review, and approve analytical method validation reports, protocols, and SOPs.
• Ensure all laboratory activities comply with current Good Manufacturing Practices (cGMP) and relevant regulatory requirements.
• Maintain laboratory equipment and instrumentation, ensuring proper calibration and performance.
• Contribute to regulatory filings and respond to queries from health authorities.
• Mentor and train junior QC scientists and analysts.
• Participate in internal and external audits as required.
• Stay current with scientific literature, industry trends, and advancements in analytical techniques relevant to pharmaceutical QC.

• Master's or Ph.D. in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or a related field.
• Minimum of 5-7 years of hands-on experience in pharmaceutical quality control and analytical method development/validation.
• Extensive experience with HPLC, GC, dissolution apparatus, and other relevant analytical instrumentation.
• Thorough understanding of cGMP, ICH guidelines, and pharmacopeial standards (USP, EP, JP).
• Excellent documentation skills, with the ability to write clear, concise, and compliant reports and protocols.
• Strong problem-solving and critical thinking abilities.
• Proficiency in data analysis and interpretation.
• Excellent communication and interpersonal skills, crucial for remote collaboration.
• Experience with laboratory information management systems (LIMS) is a plus.