1,449 Quality Control Specialists jobs in India

About the Company

As the world’s leading multidisciplinary service provider, Deluxe underpins the media and entertainment industry, servicing content creators and distributors including Netflix, Warner Media, The Walt Disney Company, Amazon, Apple, Viacom, NBCU, Google, AT&T and many others, by providing Global Content Distribution, Localization, Accessibility and Mastering while leading end-to-end innovation with unparalleled scale and agility across the Streaming, Theatrical, Broadcast and Mobile landscapes. With headquarters in Los Angeles and offices around the globe, the company employs over 3,200 of the most talented and experienced industry individuals worldwide. For more information, please visit

Position Overview

Performing Technical checks on files daily, on various file types. Ensuring our subtitles conform to industry and Deluxe standards and client requirements (timing, formatting, and language and client specific rules) and ensuring 100% on-time delivery, while maintaining an average quality record of 99%.

Primary Responsibilities

• Checking that language subtitles conform to Deluxe guidelines and meet the specific client requirements.
• Ensuring that these subtitles are checked against reference material related to the project and

implementing required instructions to ensure that the final product is consistent and errorfree

• Ensuring that the quality of work is very high with less than 1% error rate, thus maintaining an average quality yield of nothing less than 99% throughout the year, for all clients.
• Updating work trackers to denote accurate status of projects.
• Ensuring 100% on-time delivery for all clients.
• Coordinating with PC and updating Project Notes to implement changes or fixes in languages, based on errors found.
• Providing feedback to other users and departments, when standard procedure is not followed, so that quality measures are implemented upstream as well.
• Communicate clearly and effectively with clients, both internal / external.
• Should take ownership of one's work.
• Follow department specific schedules, guidelines and demonstrate schedule adherence, and attendance.

Additional Responsibilities

• Mentoring and coaching newer recruits to bring them up to the expected quality standards set

by the department.

• Promote teamwork.
• Suggest improvements to the platform or any of the subtitling workflows during your work.
• Actively participate in all job / personal knowledge training programs.
• Display eagerness and willingness to learn other aspects of the process such as task assignments, process evaluation, etc., that contribute eventually to individual growth

Skills & Personal Attributes

• Exceptional audio sensitivity – ability to understand a variety of English accents.
• Good comprehension and communication skills.
• Broad cultural knowledge and wide range of interests.
• Team player, detail-oriented, ability to multi-task and work under tight deadline.
• Technically proficient in Microsoft Office, including Word, Excel, Outlook, Access, PowerPoint.
• Good knowledge of Computers and internet.
• Good typing speed and accuracy.
• Broad cultural knowledge and wide range of interests.
• Should be Accountable / Dependable
• Should possess Analytical Thinking & Problem-Solving skills
• Should be methodical, possess a disciplined work approach and have an eye for detail.

**Candidates should be flexiable to work from our office location (Bellandur, Bangalore) and ready to work in night shift**

• 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 maintain comprehensive quality control plans and procedures.
• Conduct routine inspections and testing of raw materials, in-process materials, and finished products.
• Analyze test results, identify deviations from specifications, and initiate corrective actions.
• Collaborate with production and engineering teams to identify root causes of quality issues and implement solutions.
• Maintain accurate quality records, documentation, and reports.
• Monitor and analyze production processes using statistical methods (SPC) to ensure consistency and identify trends.
• Ensure compliance with all relevant quality standards, industry regulations, and customer requirements.
• Participate in internal and external quality audits.
• Contribute to continuous improvement initiatives to enhance product quality and process efficiency.
• Stay updated on advancements in quality control techniques and technologies.
• Train production staff on quality standards and procedures as needed.

• Bachelor's degree in Engineering (Mechanical, Chemical, Industrial) or a related technical field.
• Minimum of 4 years of experience in quality control or quality assurance within a manufacturing or production environment.
• Proficiency in quality management systems (e.g., ISO 9001) and methodologies.
• Experience with statistical process control (SPC) software and techniques.
• Strong analytical and problem-solving skills, with a keen eye for detail.
• Excellent documentation and reporting skills.
• Effective communication and interpersonal skills, essential for remote collaboration.
• Ability to work independently, prioritize tasks, and manage time effectively in a remote setting.
• Familiarity with relevant industry-specific quality standards is a plus.
• Proficiency in standard office software (e.g., MS Office Suite).

• Develop, validate, and transfer analytical methods for pharmaceutical raw materials, intermediates, and finished products.
• Perform routine testing of raw materials, in-process samples, and finished products according to established specifications and protocols.
• Operate and maintain various analytical instruments, including HPLC, GC, FTIR, UV-Vis, and dissolution apparatus.
• Interpret analytical data, troubleshoot instrument issues, and resolve Out-of-Specification (OOS) results.
• Ensure compliance with GMP, GLP, and relevant pharmacopoeial standards.
• Collaborate with manufacturing and R&D teams to address product quality issues and support process improvements.
• Prepare analytical reports, method validation protocols, and summary reports.
• Participate in internal and external audits as a subject matter expert.
• Maintain accurate and complete laboratory records and documentation.
• Stay current with advances in analytical techniques and regulatory expectations.

• Master's or Ph.D. in Analytical Chemistry, Pharmaceutical Chemistry, or a related scientific discipline.
• Minimum of 7 years of experience in pharmaceutical quality control and analytical development.
• Extensive hands-on experience with various analytical techniques, particularly HPLC and GC.
• Proven experience in method development and validation according to ICH guidelines.
• Strong understanding of GMP, GLP, and pharmacopoeial requirements.
• Proficiency in using laboratory information management systems (LIMS).
• Excellent analytical, problem-solving, and critical thinking skills.
• Meticulous attention to detail and strong organizational abilities.
• Effective written and verbal communication skills for reporting and collaboration.
• Ability to work independently and manage workload effectively in a remote setting.
• Experience in **pharmaceutical quality control** and **analytical chemistry** within the **Chennai, Tamil Nadu, IN** pharmaceutical landscape.

• Reviewing and analyzing sanitation logs, checklists, and inspection reports.
• Conducting virtual audits of sanitation practices and procedures based on provided documentation and evidence.
• Ensuring compliance with health, safety, and environmental regulations.
• Identifying deviations from quality standards and recommending corrective actions.
• Providing detailed feedback and reports to management and on-site teams.
• Assisting in the development and updating of sanitation protocols and training materials.
• Monitoring key performance indicators (KPIs) related to sanitation quality.
• Communicating effectively with field staff to gather information and address concerns.
• Maintaining accurate records of audits and quality control activities.
• Staying updated on industry best practices and emerging trends in sanitation and hygiene.

• Reviewing and approving or rejecting raw materials, in-process materials, and finished products based on established specifications and testing results.
• Analyzing and interpreting laboratory test data to ensure compliance with pharmacopeial standards and internal quality control procedures.
• Investigating deviations, out-of-specification (OOS) results, and customer complaints, identifying root causes and recommending corrective and preventive actions (CAPAs).
• Collaborating with manufacturing, R&D, and regulatory affairs departments to resolve quality issues and ensure product consistency.
• Participating in the development, validation, and transfer of analytical methods.
• Maintaining accurate and complete quality control records, including batch records, testing data, and deviation reports.
• Ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
• Contributing to internal and external audits by preparing relevant documentation and providing information as requested.
• Assisting in the qualification and calibration of laboratory equipment.
• Participating in risk assessments and quality management initiatives.

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
• Operate and maintain laboratory equipment such as HPLC, GC, and Spectrophotometers.
• Interpret test results and investigate deviations and OOS results.
• Document all laboratory activities in compliance with GMP and GLP.
• Conduct method validation and stability studies.
• Contribute to the development and implementation of CAPA plans.
• Mentor and train junior QC personnel.
• Ensure laboratory equipment is calibrated and maintained.
• Collaborate with cross-functional teams on quality-related matters.

• Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field.
• 5+ years of experience in pharmaceutical quality control or quality assurance.
• In-depth knowledge of analytical techniques (HPLC, GC, UV-Vis, FTIR).
• Familiarity with pharmaceutical regulatory guidelines (ICH, FDA, WHO).
• Strong understanding of GMP and GLP principles.
• Excellent documentation and record-keeping skills.
• Proficiency in data analysis and interpretation.
• Strong problem-solving and critical thinking abilities.
• Effective communication and interpersonal skills.

• Conduct inspections of raw materials, in-process products, and finished goods according to established quality control procedures.
• Perform dimensional, visual, and functional tests on automotive components using various measurement tools and equipment.
• Identify, document, and report non-conforming products or process deviations.
• Collaborate with production teams to implement corrective actions and prevent recurrence of defects.
• Monitor production processes to ensure adherence to quality standards and specifications.
• Analyze quality data, identify trends, and generate reports for management review.
• Participate in internal and external audits to ensure compliance with quality management systems (e.g., ISO/TS 16949).
• Maintain calibration records for all quality control equipment.
• Assist in the development and improvement of quality control procedures and work instructions.
• Support new product introduction by ensuring quality requirements are met.
• Provide training to production personnel on quality standards and inspection techniques.
• Handle customer complaints related to product quality and support investigation.
• Ensure a clean and organized work environment within the quality control area.
• Contribute to continuous improvement initiatives within the manufacturing operations.
• Uphold company policies and safety regulations at all times.

• Diploma or Bachelor's degree in Mechanical Engineering, Manufacturing Technology, or a related technical field.
• Minimum of 3 years of experience in quality control within the automotive manufacturing sector.
• Proficiency in using precision measuring instruments such as calipers, micrometers, gauges, and CMMs.
• Solid understanding of quality control principles, statistical process control (SPC), and problem-solving tools (e.g., 8D, Pareto analysis).
• Experience with quality management systems like ISO 9001 or IATF 16949.
• Ability to read and interpret technical drawings, specifications, and blueprints.
• Strong analytical and problem-solving skills.
• Good communication and interpersonal skills, with the ability to work effectively with different departments.
• Attention to detail and a commitment to accuracy.
• Basic computer skills, including MS Office.
• Physical ability to stand for extended periods and lift moderately heavy items if required.