Quality Analyst Graduate Jobs in Hyderabad

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QA tools and software.# Immediate joiners preferred.Offered Salary:Upto 6 LPA (hike as per company norms based on last withdrawn)How to Apply:Share your CV with me at AK00908688@TechMahindra.comDon't forget to mention Job Title (IQA-Hyd) while applying!#TechMahindra #hyderabadjobs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

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.

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

After 45 days of free training (technical) followed by 15 days (non technical), candidates can be placed in pharma company. During training candidate need to take care of living expenses including food accomodation and local travel.

Diamond Assorter From Jewelry Background3 + years experienced in Diamond assorting and person with an eye for detail with in depth knowledge of Cut Clarity and color of Diamonds.

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.

Responsible for planning and delivering development related projects according to the established goals, while working with regulatory, BD, analytical, QC, QA Must have an understanding of relevant methodologies, processes and standards and ensure that all project team members understand and follow these. Experience in developing, reviewing and approving cGMP and ISO related documents (SOPs, protocols, reports, etc) To complete the sample request from different customer which include sample preparation, documentation, COA preparation, packing and dispatch of free sample to the customer and maintain all the required and supporting document. To cater and address different Vendor Qualification Documentation requirement like VQ questionnaire, quality agreements, declaration of regulatory compliance documents against the request came from different customer. Investigates and conducts root cause analysis of deviations and out of specification results for non-validated or under development procedures. Review and update standard operating procedures (SOPs) to align with changing regulations and best practices. Documentation And Records Management Maintain and manage documentation related to quality assurance activities, including batch records, investigation reports, change controls, and validation documentation. Reviewing and approving compliance reports following external (customer/regulatory) audits and corporate audits to ensure compliance. Prepared & Review of Validation protocol and report (like Process Validation, Cleaning Validation, Analytical Method Validation,) Identifying the Incomplete and inadequate data, and Addressing the same for resolve. Ensure the data is accurate, reliable and sustainable.

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

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.

Every Day 3 to 5 Hours Classes .if Online Can Be Taken Class from Your Own Place

Should be able to own couple of projects and do hands-on work in an IC role. Also provide guidance to other team members to generate the QA test strategy Has good knowledge of functional, regression testing.Hands on with API testing,Has hands-on understanding of Complex SQL queries with JoinsAble to understand ER diagram, DB schemaHas worked on ETL, BI and Data warehousing projectsHas worked in projects using multiple data source and data processing of OLTP Dbparticipate in everyday scrum, update on your daily task progress, highlight risks and suggest mitigation plansYou will work with team members in India and in the US/CanadaYou will do demo of product features to the clientsYou will participate in discussions on architecture, project requirement and test strategy.

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.