Quality Analyst Female Graduate Jobs in Hyderabad

As data Analyst at Krisantec Solutions, you will leverage data to help our clients make informed business decisions. Your ability to interpret and analyze large datasets will be critical in helping the team provide actionable insights. This role is ideal for someone who thrives on data storytelling, problem-solving, and delivering results.

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QA tools and software.# Immediate joiners preferred.Offered Salary:Upto 6 LPA (hike as per company norms based on last withdrawn)How to Apply:Share your CV with me at AK00908688@TechMahindra.comDon't forget to mention Job Title (IQA-Hyd) while applying!#TechMahindra #hyderabadjobs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

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

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.

We are seeking experienced Quality Management (QM) End User Experts with 5 to 8 years of relevant experience in managing quality processes within SAP systems. Candidates should have hands-on experience in data feeding, quality management, and handling quality control operations. Experience in the Pharma industry is preferred. This is an excellent opportunity for professionals looking to grow in the SAP Quality Management domain.Key Requirements: 5 to 8 years of experience as a QM End User, with a focus on quality management processes. Hands-on experience managing quality control processes and operations using SAP S/4 HANA. Proficient in data management within SAP Quality Management (QM). Experience in the Pharma industry is preferred. Basic understanding of SAP systems and QM modules. Strong attention to detail and the ability to manage quality-related datasets. Good communication and teamwork skills. Ability to work independently and manage tasks efficiently.Key Responsibilities: Perform data entry, quality data feeding, and quality control management tasks within the SAP QM module. Ensure the accuracy and integrity of quality data in SAP systems. Collaborate with production, quality control, and other departments to ensure smooth data flow and process execution. Assist in preparing reports and documentation related to quality management activities. Troubleshoot and resolve data discrepancies and issues within the SAP QM system. Support quality assurance and production teams with SAP-related queries and tasks. Participate in system upgrades and testing related to SAP QM processes.Preferred Qualifications: Familiarity with SAP modules like MM (Material Management) and PP (Production Planning) is a plus. Prior experience in the quality management or quality control field is preferred.Work Environment: Based in Hyderabad with a collaborative work environment. Opportunities for professional growth and development within the com

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.

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

Greetings from Starworth Global Solutions!Hiring for AR-QA Job Position: Quality analyst Location Bangalore, Chennai, HyderabadQualification: Graduates are eligible.Max salary for QA-Bangalore and Chennai-Upto 50kHyderabad - Upto 47k Should have acted as QA in the previous company . Minimum 4+ years of Experience in AR calling is Mandatory. Excellent domain knowledge and Exposure in quality aspects. Experience : Expertise in AR domain/ Denial Management- Physician Billing / Hospital Billing Joining : Immediate/ or a max of 10-15 days Work Mode : Work from Office Night shifts Company will provide a weeks accommodation for candidates relocating from other cities. The salary package will commensurate with industry standards basis their current CTC and years of relevant experience. Week Off Details: Fixed off on Saturdays & Sundays Cab facility: 2-way cab available ( For night shifts/ Compulsory to be availed by Women Employees)Rounds of Interview: 1st Round - HR Round ( screening by TA team / will be conducted over teams.)2nd Round - Operations Round( Assessment by Ops Managers/ will be conducted over teams.)

Good Communication in written & Oral.Hand on experience in QA in a non voice process.Should have 1-3 year experience in BPO.Must hand on experience on Chat, Document Verification, E-Mail support (Non Voice).Open work in rotational shifts.Should be fluencet in Telugu.Can join immediate or 15 Days max.

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