1,346 Qc Analyst jobs in India

Role

• Working on maintaining consistency of terminology while transcribing
• Creating/ Quality assuring, proofreading and editing final transcribed versions with strong US and UK accents and providing feedback as necessary to team members
• Providing process improvement ideas for faster and quality output
• Researching idioms, technical content, colloquial expressions etc. using various online resources, dictionaries and thesauruses to find the correct contextual transcription.

Job Requirement

• Strong in English transcription with US and UK accents
• Good typing skills
• Strong English comprehension
• He/she should have work experience in English content writing, transcription, copywriting, trans-creation, editing and knowledge of multiple subtitling/captioning tools like, Subtitle Edit, Subtitle Workshop, etc.
• He/she should have an in-depth knowledge of English grammar and flow and related culture required for localization.
• Presence on Social Media Sites, blogging in English and international languages will be an advantage.
• He/She should work as a team player with production team with full support and involvement.
• He/She should have respect towards deadlines to avoid misses.
• Should be flexible to work in shifts.

Education and Experience:

• Bachelor’s Degree in Languages/Translation/Transcription/Computational Linguistics, or equivalent experience.
• 3+ years in English transcription, subtitling/captioning process with knowledge of multiple subtitling/captioning tool like Subtitle Edit, Subtitle Workshop, etc.
• Have worked on technical and creative contents previously.

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
• Operate and maintain laboratory instruments (HPLC, GC, UV-Vis, etc.).
• Document all test results and maintain accurate laboratory records.
• Ensure compliance with GLP, GMP, and relevant regulatory guidelines.
• Conduct method validation and stability studies.
• Investigate out-of-specification (OOS) results and deviations.
• Prepare Certificates of Analysis (CoA).
• Collaborate with R&D, Production, and Regulatory Affairs teams.
• Participate in internal and external audits.
• Contribute to process improvement initiatives within the QC department.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
• Proven experience as a Quality Control Analyst in the pharmaceutical industry.
• Hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis).
• Strong knowledge of pharmaceutical quality systems and regulations.
• Excellent analytical and problem-solving skills.
• Meticulous attention to detail and record-keeping.
• Ability to work effectively in a laboratory setting and meet deadlines.
• Good communication and teamwork skills.
• Familiarity with method validation principles.
• Experience with OOS investigations and CAPA.

• Perform routine and non-routine analytical tests on raw materials, intermediates, and finished products.
• Operate and maintain laboratory equipment such as HPLC, GC, FTIR, UV-Vis, and dissolution apparatus.
• Analyze samples using validated methods and ensure compliance with pharmacopoeial standards.
• Document all laboratory activities, results, and observations accurately and contemporaneously.
• Investigate out-of-specification (OOS) results and deviations, and implement corrective and preventive actions (CAPA).
• Prepare certificates of analysis (CoA) and other quality control reports.
• Ensure adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Participate in method validation and transfer activities.
• Maintain laboratory inventory and ensure proper storage of reagents and samples.
• Collaborate with Quality Assurance and Production teams on quality-related issues.
• Stay updated with the latest regulatory guidelines and scientific advancements in pharmaceutical quality control.
• Contribute to continuous improvement initiatives within the QC department.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 4-6 years of experience in a pharmaceutical Quality Control laboratory setting.
• Hands-on experience with analytical instrumentation (HPLC, GC, etc.).
• Thorough understanding of GMP, GLP, and regulatory requirements.
• Proficiency in data analysis and interpretation.
• Strong attention to detail and accuracy.
• Excellent problem-solving and investigative skills.
• Good written and verbal communication skills.
• Ability to work effectively in a team environment.

• Conduct analytical testing on pharmaceutical raw materials, intermediates, and finished products.
• Utilize various analytical instruments like HPLC, GC, and spectrophotometers.
• Document all laboratory activities and results according to GMP and GLP.
• Participate in method validation and stability studies.
• Investigate and report out-of-specification (OOS) results.
• Maintain laboratory equipment and ensure proper calibration.
• Prepare reagents and samples for testing.
• Collaborate with Quality Assurance for product release.
• Adhere to all safety and environmental protocols in the laboratory.
• Contribute to continuous improvement initiatives in the QC department.

• Perform routine and non-routine analytical testing using a variety of laboratory techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
• Analyze samples of raw materials, intermediates, and finished pharmaceutical products.
• Document all laboratory activities, results, and observations accurately and in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Prepare reagents, standards, and samples for testing.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and calibration records.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Assist in the validation and qualification of analytical methods and equipment.
• Review and approve test results and associated documentation.
• Maintain a clean and organized laboratory environment.
• Stay updated on pharmacopoeial standards (e.g., IP, BP, USP) and regulatory guidelines.
• Contribute to the continuous improvement of quality control processes.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Microbiology, or a related life science discipline.
• Minimum of 3-5 years of experience in a pharmaceutical Quality Control laboratory.
• Proficiency in analytical techniques such as HPLC, GC, and wet chemistry.
• Thorough understanding of GLP, GMP, and relevant regulatory guidelines.
• Experience with laboratory information management systems (LIMS) is a plus.
• Strong attention to detail and accuracy in data recording and analysis.
• Excellent organizational and time management skills.
• Ability to work independently and as part of a team.
• Good written and verbal communication skills.
• Proficiency in Microsoft Office Suite.

• Performing analytical tests on raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
• Analyzing test results and comparing them against established specifications and regulatory standards.
• Documenting all testing procedures, results, and observations accurately in laboratory notebooks and electronic systems.
• Identifying and investigating any deviations from established specifications or procedures.
• Participating in method validation and transfer activities.
• Preparing and standardizing reagents and solutions for analytical testing.
• Calibrating and maintaining laboratory equipment to ensure accurate and reliable results.
• Ensuring compliance with all safety regulations and environmental policies.
• Assisting in the investigation of out-of-specification (OOS) results.
• Contributing to the continuous improvement of quality control processes.
• Collaborating with production and R&D teams to resolve quality-related issues.
• Maintaining a clean and organized laboratory environment.

• Perform routine and advanced 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 transfer analytical methods according to established protocols and regulatory guidelines.
• Analyze test results, interpret data, and prepare accurate and comprehensive reports.
• Investigate out-of-specification (OOS) results and deviations, documenting findings and recommending corrective and preventive actions (CAPA).
• Maintain laboratory equipment, ensuring calibration, qualification, and routine maintenance are performed.
• Ensure adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory standards.
• Prepare and review standard operating procedures (SOPs) for analytical testing and laboratory operations.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues and support product development.
• Manage laboratory inventory, including chemicals, reagents, and consumables.
• Participate in internal and external audits as required.
• Stay updated with the latest advancements in pharmaceutical analysis and quality control techniques.
• Contribute to continuous improvement initiatives within the Quality Control department.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
• Extensive hands-on experience with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
• Proficiency in wet chemistry techniques and compendial testing (USP/EP/BP/IP).
• Strong understanding of GMP, GLP, and ICH guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Meticulous attention to detail and accuracy in data recording and reporting.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.
• Proficient in Microsoft Office Suite and LIMS (Laboratory Information Management System) software.
• Strong written and verbal communication skills.
• Experience with method validation and transfer is highly desirable.