Array ( [0] => quality-control-analyst [1] => hyderabad ) Quality Control Analyst Jobs in Hyderabad,QC Analyst Job Vacancies in Hyderabad Telangana
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Quality Control Analyst Job Vacancies in Hyderabad

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Quality Analyst

Tech Mahindra

  • 2 - 5 yrs
  • Hyderabad
Quality Auditing Root Cause Calibration Quality Control Tools Quality Analysis
Independent Quality Analyst (iQA) - Hyderabad (Content Moderation Focus)About the Role:In this role, you will be responsible for ensuring the quality and accuracy of videos showcasing products for purchase. This involves monitoring videos to verify that featured items are correctly tagged and linked in descriptions, allowing viewers to easily find and buy these products on eCommerce platforms. You will assess the adherence to company standards and client expectations while handling potentially sensitive content with professionalism.Key Responsibilities:# Quality Monitoring: Review videos where content creators showcase products like watches, clothing, furniture, and appliances. Ensure that all featured products are properly tagged and linked in the video descriptions for easy purchase on eCommerce platforms.# Tagging and Linking Verification: Verify that all products shown in the video are accurately tagged and linked in the video description. Ensure that links direct viewers to the correct eCommerce platforms and product pages.Requirements:# 2+ years of quality assurance (QA) experience in moderation.# Bachelor's Degree or equivalent.# Ready to work from office (Bahadurpally-Hyd).# 5 days working. Ready to work for rotational shift.# Experience with content that features products for purchase.# Experience in content creation/moderation for social media.# Proficiency in QA tools and software.# Immediate joiners preferred.Offered Salary:Upto 6 LPA (hike as per company norms based on last withdrawn)How to Apply:Share your CV with me at AK00908688@TechMahindra.comDon't forget to mention Job Title (IQA-Hyd) while applying!#TechMahindra #hyderabadjobs #ContentModerator #QAhiring #QAcontentModeration #techmahindratiring #Hyderabadhiring #CoMojobs #ContentModeration
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Quality Control Inspector

Vidhata Plastics India Pvt Ltd

  • 1 - 3 yrs
  • 3.3 Lac/Yr
  • Hyderabad
Quality Analyst Quality Assurance Analyst Quality Control Analyst Quality Control Engineer Quality Control Manager Quality Control Inspector Quality Controller Quality Control
Hi all,We are currently hiring for the following position on an urgent basis. If anyone is interested in joining immediately, send your latest resume to the email id below.Company: Vidhata Plastics India Pvt LtdJob Location: S-1 P/C, Survey No: 114, E-City, Maheshwaram, Ranga Reddy, Hyderabad, Telangana, 501359Email Id: hr@vidhata.co.inPosition Name: Quality InspectorNo. of years exp required: 1 to 2 years.Min. Qualification: Intermediate/ITI/DiplomaNo of Positions: 1Job Description: Tool Room inspectionSalary: 15000 18000 (Salary is negotiable based on experience)Benefits: PF & Health Insurance
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Quality Control Analyst

Kreative Organics Private Limited

  • 3 - 6 yrs
  • 5.0 Lac/Yr
  • Hyderabad
Pharma Quality Control HPLC Quality Analysis Empower Software Method Development Pharma Quality Walk in
1. To ensure compliance with Good laboratory practices and Good manufacturing practices.2. Should be follow laboratory safety personal protective equipments while handling analysis.3. Based on work allocation analysis should be perform and same day document completion.4. All the analysis of raw materials, in-process, intermediate, stability, Recovery solvents, R&Dsamples and finished product HPLC and GC analysis as per procedure.5. All working standards HPLC and GC related analysis planned as per schedule date.6. Working standard should be use by ensuring validity of standard within the period.7. Chemist should be ensuring before using the instrument status and calibration of instrumentand earlier analysis results should be ensure.8. Chemist should be ensure before starting analysis availability of standards, chemicals andglasswares etc.,9. Analyst should follow good laboratory practices laid down in the quality control laboratory.10. Analyst should follow after completion of chromatography analysis ensure the results anddiscard the solutions if results within the specification.11. Analyst once started the sequence set of sample loading same day next day need to processyesterday samples then only go for new work.12. Analyst should process the samples contemporaneously if any abnormal results observedinform immediately senior supervisor/reviewer/designee then only next decision to be taken.13. Analyst is responsible for analysis and documentation and sample disposition.14. Analyst is responsible for laboratory cleaning, instrument cleaning and maintenance in goodcondition.15. Results are reported as per rounding of the SOP.16. Equipments calibration shall be performed as per internal calibration master schedule.17. After usage of the working standards and reference standards it shall be kept in designatedplace.18. Monitoring the daily room temperature and its recording as per procedure.
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Quality Control Analyst

Bhagyavati Placement & Services

Microsoft Office Pharma Quality Control HPLC Quality Analysis
Quality Control Analyst RoleWe are seeking a Quality Control Analyst to ensure the consistent quality of our production output. In this role, you will conduct laboratory tests on incoming raw materials, in-process production samples, and final products before distribution. You will analyse data to ensure product specifications are met and perform peer reviews of other analyses. As part of this role, you will also review current GMP documentation relating to testing methods and regulations and implement ways that we can update or improve our processes. Applicants should have a bachelors degree in chemistry, biochemistry, or another biological sciences field.Quality Control Analyst DutiesPerform QC testing on raw materials, in-process items, and final productsAssess data to make sure product specifications are metReview good manufacturing practise documentation, including test methods and protocolsPerform review of test data and analysisMaintain inventory of testing suppliesSupport process improvementMaintain laboratory equipmentQuality Control Analyst RequirementsBachelors degree in chemistry, biochemistry, or another biological sciences fieldMasters degree a plusAnalytical skillsFamiliarity with Industry standards and regulationsClinical laboratory experience preferred
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QC Analyst

Issar pharmaceuticals private limited

  • 3 - 5 yrs
  • 6.5 Lac/Yr
  • Greater Hyderabad
Complete Knowledge Of Operation Good Documentation QC Chemist QC Analyst Documentation Analyst HPLC LCMS
The candidate should have complete Knowledge of operation and familiarity of various instruments including HPLC, LCMS, GC, and TOC with Good documentation and timely analysis and recording of stability data.
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  • 5 - 8 yrs
  • 20.0 Lac/Yr
  • Hyderabad
Quality Assistant Quality Assurance Analyst Quality Associate QA QC Engineer Walk in
DetailsHands-on overall minimum experience of 5 years in Testing.Proficient experience of minimum 2-3 years in Manual Testing.Proficient experience of minimum 2 years in Automation testing tool i.e Selenium.Minimum 2 years in any programming language like Java(Preferably)Working experience in Agile methodology * Identify the tools for Test Reporting, Test Management, Test Automation, etc. andeducate the team on how to use those tools. Again, plan knowledge transfer sessions ifrequired to the team members for the tools that they would use.*During the Testing Cycle, monitor the test progress by constantly assessing the workassigned to each of the resources and re-balance or re-allocate them as required.* Identify the testing effort required by calculating the sizing needed for the given releaseand plan the required effort for the same.
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LAB Analyst Chemical Engineer Chemist Microbiologist Pharmaceutical Production Pharmacy QC Walk in
Job descriptionWANTED Chemical, FMCG, Polymer, Plastic, Rubber, Petroleum Products & Pharma - Manufacturing Sectors hiring people for the following departments:- PRODUCTION / PROCESS / QC / LAB ANALYSTM / F, Fresh / Exp., Age : 18-35 Yrs.Eligibility :-Diploma's/ Engineers / Graduate's(B.Sc. / M.Sc) Graduates - Batches: 2017 - 2020.Desired Candidates are willing to work anywhere in India.Role Pharmacist/Chemist/Bio ChemistIndustry Type Pharma / Biotech / Clinical ResearchFunctional Area Medical, Healthcare, R&D, Pharmaceuticals, BiotechnologyEducationUG : B.Pharma - Pharmacy, B.Sc - General, Environmental science, Food Technology, Agriculture, Geology, Anthropology, Home science, Bio-Chemistry, Biology, Microbiology, Botany, Chemistry, Dairy Technology, Zoology, Diploma - Chemical, Vocational Course, B.Tech/B.E. - Petroleum, Environmental, Production/Industrial, Textile, Bio-Chemistry/Bio-Technology, Biomedical, Ceramics, Chemical, PG : M.Tech - Chemical, Petroleum, Agriculture, Environmental, Production/Industrial, Textile, Bio-Chemistry/Bio-Technology, Biomedical, Ceramics, MS/M.Sc(Science) - Botany, Chemistry, Dairy Technology, Zoology, Environmental science, Food Technology, Agriculture, Geology, Anthropology, Home science, Bio-Chemistry, Biology, Microbiology, M.Pharma - Pharmacy, PG Diploma - Chemical
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  • 1 - 4 yrs
  • 3.8 Lac/Yr
  • Jeedimetla Hyderabad
Analytical Chemist Quality Control Walk in
Kreative Organics Private Limited is a manufacturer of Active Pharmaceutical Ingredients (APIs) for the world market. Kreative started operations in 1990.Kreative was established by Dr. S. Krishnamohan. Dr. Krishnamohan was formerly with TIFR, BARC, Caltech and NASA. He is a scientist of international repute and runs Kreative with professionalism and a focus on innovation.Kreative maintains strict quality standards and has developed a robust quality system around which all of our products are manufactured.Kreative invested in a state of the art cGMP facility in 2005 and expanded it to a US FDA class facility in 2013.Kreative, is WHO GMP certified and has successfully been audited by the US FDA in Feb 2020.
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Quality Assurance Analyst

Kreative Organics Private Limited

  • 5 - 9 yrs
  • 6.0 Lac/Yr
  • Jeedimetla Hyderabad
Communication Skills Organic Chemistry Method Development Change Control OOS & OOT Investigations Of Incidents Quarterly & Annual Calibrations Schedules Stability Study Initiation AS Part Of CCF Review Of IM FP AWS Records Master STP Relevant Work Sheet AR Review Quality Analyst QMS
1. Master STP and relevant work sheet and AR review/ revision.2. Analytical Method validation protocol, monitoring and report (9 No's - 2020)3. Investigations of incidents (139 No's - 2020)4. QC SOP revision (Review, Print, signature followup)5. Review of daly, monthly, quarterly and annual calibrations and schedules.6. Organized data backup as per the schedule7. Stablity study initiation as part of CCF/ Add on batch. accordingly protocols to be review and approval8. Review of IM & FP AWS recordsQMS:12. Change control handling (66 No's)13. Deviation Handling14. OOS handling15. Weekly meeting preparation16. MRM preparation17. Audit support.18. CAPA followup19. CAPA effectiveness20. Internal audits followup and closure
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