Top Quality Control Analyst Skills

Below we've compiled a list of the most important skills for a Quality Control Analyst. We ranked the top skills based on the percentage of Quality Control Analyst resumes they appeared on. For example, 10.5% of Quality Control Analyst resumes contained Lab Equipment as a skill. Let's find out what skills a Quality Control Analyst actually needs in order to be successful in the workplace.

The six most common skills found on Quality Control Analyst resumes in 2020. Read below to see the full list.

1. Lab Equipment

high Demand
Here's how Lab Equipment is used in Quality Control Analyst jobs:
  • Performed day-to-day maintenance and troubleshooting of lab equipment/instruments.
  • Performed general lab and equipment maintenance duties such as sterility core cleaning and periodic cleaning and maintenance of lab equipment.
  • Utilized and calibrated all lab equipment in a timely and accurate manner to ensure reliable results during product testing.
  • Performed routine QC responsibilities such as lab equipment maintenance, QC inventory control, and reconciliation of samples.
  • Assisted Senior Microbiologist with the design of the Installation/Qualification (IQ/OQ) protocol for new lab equipment.
  • Maintain, troubleshoot, investigate lab equipment to reduce recurring problems and improve throughput and cycle time.
  • Maintained and handled lab equipment and devices, which includes calibrations, proper storage and maintenance.
  • Coordinate the use of lab equipment and testing devices with other lab and management personnel.
  • Assist technicians with installation, repair, and maintenance of lab equipment and devices.
  • Support execution of validations for lab equipment, Lab methods and/or facility projects.
  • Clean and maintain lab equipment and sterility suite to ensure ISO 9000 compliance.
  • Completed validation projects on any new kit, reagent, or lab equipment.
  • Set up and maintained Instrumentation Program for the Quality Control lab equipment.
  • Performed tests and monitored lab equipment for 100% output accuracy rate.
  • Operate and calibrate lab equipment; conduct troubleshooting and preventive maintenance.
  • Test and audit new procedures, calculations, and lab equipment.
  • Calibrate lab equipment's as per plan and maintain records.
  • Calibrated, maintained and kept an inventory of lab equipment.
  • Trained new employees on various types of lab equipment.
  • Complete maintenance and calibration on lab Equipment.

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2. Test Procedures

high Demand
Here's how Test Procedures is used in Quality Control Analyst jobs:
  • Performed basic test procedures for raw materials and reviewed test results for accuracy prior to submitting documentation reports.
  • Compiled and reported data for documentation of test procedures and performed investigations on OOS results.
  • Compiled data for documentation of test procedures and prepared reports.
  • Followed good documentation practices for documentation of test procedures.
  • Monitored chemical and physical test procedures and results.
  • Compiled data for documentation of test procedures and prepared precise technical reports, summaries, protocols, and quantitative analyses.
  • Compiled data for documentation of test procedures of chemical assays, stability program testing, and formulation studies.
  • Execute and documents test procedures of raw materials prior to production release.
  • Organized test procedures and executing tests in Web and Client/Server Environments.
  • Developed new test procedures as well as improving current test procedures.
  • Drafted and revised all enzyme test procedures.
  • Coordinated review of Supplier Test Procedures.
  • Compiled data for documentation of test procedures and reported abnormalities Reviewed data obtained for compliance with specifications
  • Docummented test procedures and developed testing methods.
  • Prepared Analytical Test Procedures and Documents.
  • Train new employees on departmental test procedures and maintain training records, maintain equipment calibration program.
  • Designed and delivered a stability program (SOPs and Test Procedures) for cGMP facility

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3. Ensure Compliance

high Demand
Here's how Ensure Compliance is used in Quality Control Analyst jobs:
  • Perform quality control testing and monitoring to ensure adherence to established policies and procedures; also ensure compliance with state/federal regulations.
  • Prepare and organize laboratory department policies and procedures to ensure compliance with regulatory standards and hospital Administrative standards.
  • Conducted training sessions for operations personnel to ensure compliance with the policies and procedures and regulatory requirements.
  • Perform and document periodic compliance reviews to ensure compliance with internal policies and applicable lending compliance regulations.
  • Perform critical evaluations of stability data to ensure compliance with global regulations and ICH guidelines.
  • Conducted internal quality audits of various departmental areas to ensure compliance with invoked procedures.
  • Complete in-process and final inspections to ensure compliance to all applicable documentation requirements.
  • Reviewed work papers to ensure compliance with client methodology and regulatory recommendations.
  • Analyzed daily new account membership applications to ensure compliance within company requirements.
  • Investigated new methodology and instrumentation to ensure compliance with QC/QA procedures.
  • Conduct laboratory documentation to review and ensure compliance.
  • Perform a variety of tests/inspections on installations at various stages of a process to ensure compliance with quality and reliability standards.
  • Analyze documentation and data related to gas distribution facilities to ensure compliance with Federal & State Codes and company standards.
  • Provided risk guidance in overseeing and maintaining department standards to ensure compliance was being maintained within bank and federal standards.
  • Proofread and edit all outgoing letters to customers disputing charges to ensure compliance with Federal Regulation Z and internal guidelines.
  • Reviewed all financial transactions to ensure compliance with national guidelines and NY Regulation 60 requirements for our New York segment.
  • Counted and documented quarterly cash-on-hand reviews for the Commissary and Alabama National Guard to ensure compliance with Cash Holding Authority.
  • Perform customer profile reviews for investment and Global Market clients to ensure compliance with the bank's BSA/AML program.
  • Review compliance documents to ensure compliance with PHH, Client, Investor, State, Federal and Regulatory guidelines.
  • Review of Performing and Non-performing portfolio loans to ensure compliance to Master Agreements between Freddie Mac & various lenders.

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4. Raw Materials

high Demand
Here's how Raw Materials is used in Quality Control Analyst jobs:
  • Represented Raw Materials during regulatory inspections and customer audit tours, and performed audits on outsourced testing laboratories and qualified vendors.
  • Performed routine and non-routine analysis of raw materials, in process, and finished formulations according to standard operating procedures.
  • Performed various wet, physical and instrumental testing to monitor physical and chemical characteristics of raw materials and finished products.
  • Analyze raw materials, intermediates and finished products by chemical and instrumental techniques in accordance with established procedures.
  • Review and approve Certificates of Analysis for Finished Products, Pharmaceutical Finished Products and Raw Materials.
  • Analyzed raw materials, intermediates and finished products by physical, instrument and chemical analysis techniques.
  • Test assessment and analysis, standardization and validation of raw materials, intermediates and finished products.
  • Execute chemical and physical laboratory analysis of raw materials, in process and finished products.
  • Conducted physical, chemical and microbiological analyses on all raw materials and finished products.
  • Worked in quality control laboratory and ran analysis on finished products and raw materials.
  • Performed routine and non-routine analysis of in-process material, and inspected incoming raw materials.
  • Tested raw materials, intermediates and finished products using current chemistry and instrumental techniques.
  • Coordinated outsourcing of laboratory testing for third party vendor qualification for critical raw materials.
  • Release raw materials and intermediate materials by performing testing and visual inspection.
  • Initiated and implemented testing for chemical raw materials according to USP/NF/ACS requirements.
  • Conduct biological, chemical and physical analyses of incoming raw materials.
  • Sample analysis and approve incoming raw materials to support factory production.
  • Conduct analysis of raw materials and in-process and finished product formulations.
  • Performed analysis of raw materials and developed adhesives and bonding techniques.
  • Performed testing Cleaning Validation/Verification, Raw Materials and In-process samples.

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5. Analytical Methods

high Demand
Here's how Analytical Methods is used in Quality Control Analyst jobs:
  • Identified quality problems and evaluate analytical methods and procedures to determine how they might be improve and make recommendations for improvement.
  • Provided technical expertise for the development of new assays and optimization of current analytical methods.
  • Validated analytical methods and Excel calculation sheets used in QC departments across different sites.
  • Transferred and optimized analytical methods from Pharmaceutical Sciences for the in-process testing team.
  • Learned about various analytical methods used for raw material testing.
  • Authored validation reports, analytical methods and standard operating procedures.
  • Write and prepare standard operating procedure for analytical methods
  • Designed and streamlined analytical methods of new products.
  • Execute transfer validation of several analytical methods.
  • Executed water validation analytical methods, i.e.
  • Review and update standard operating procedures, protocols, reports, and analytical methods.
  • Train and develop new employees and other analysts on analytical methods and instrumentation.
  • Utilized analytical methods such as SDS-Page, western blot, raw materials testing.
  • Worked with clients to transfer, develop, and optimize analytical methods.
  • Validated and transferred analytical methods for new products in the pipeline.
  • Set up new or existing analytical methods for identifying compounds.
  • Validated analytical methods as IEF and HCP Assay.
  • Trained employees on a variety of analytical methods.
  • Initiate, revise, and approve analytical methods.
  • Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines Identify quality problems and recommend solutions.

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6. QC

high Demand
Here's how QC is used in Quality Control Analyst jobs:
  • Reviewed QC data records and notebooks to ensure conformance with approved documentation criteria and material specification.
  • Coordinated with QC and Development to manage defects and process automation updates for application enhancements.
  • Communicated issues to QC management for escalation and participated in meetings to address research options.
  • Ensured product quality by confirming accurate execution of QC testing and documenting deviations and investigations.
  • Led the weekly quality control department meetings, facilitating QC communication and project coordination.
  • Supported QC personnel during inspections or audits conducted by internal groups or regulatory agencies.
  • Performed Environmental monitoring within the QC department and during the manufacturing processes.
  • Review appraisal in conjunction with QC Checklist to verify acceptability of collateral.
  • Identify and implement issues and opportunities for improvement including new/revised QC tests.
  • Managed/maintained QC Automation lab environment, coordinating with QC and Development.
  • Created new training module that achieved QC department standardization and consistency.
  • Promoted from QC analyst to technical service and ultimately account responsibility.
  • Reviewed QC data and laboratory notebooks for completeness and accuracy.
  • Maintained database with QC data and supervised calibration program.
  • Picked up/received samples into QC Micro laboratory.
  • Prepared QC Raw Materials Specifications.
  • Assisted the QC Validation Department by performing specific validation duties and procedures required to bring new raw materials in-house for testing.
  • Provide guidance and coaching of KYC Analysts/Specialists to improve the quality output of the team based on findings in QC reviews.
  • Provide the AD with key inputs in support of complex QC challenges related to objectives and operation of the QC projects.
  • Reviewed, performed and assisted with QC sample receiving and shipping of all QC samples and special client material shipments.

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7. Stability Samples

high Demand
Here's how Stability Samples is used in Quality Control Analyst jobs:
  • Coordinated and performed instrumental analysis of drug product and stability samples.
  • Supported stability areas: submitted stability samples to the laboratory.
  • Perform testing of raw materials, drug product, clinical supplies, and stability samples per established methods and protocols.
  • Received and analyzed bulks, complaints, stability samples, special requests and finished products according to SOP and specifications.
  • Performed microbiological testing of in-process samples, drug product release and stability samples, and cleaning verification samples.
  • Tested raw materials, in-process, release, and stability samples to support drug manufacturing process.
  • Milled finished product and stability samples (tablets, capsules and powders) prior to analyses.
  • Tested In-process, final, and stability samples and reviewed Quality Control test results for accuracy.
  • Performed QC analysis on raw materials, in-process samples, and finished product and stability samples.
  • Performed testing on raw materials, in process samples, finished product, and stability samples.
  • Tested Development, Raw Materials, In-Process, Bulk, Finished Product, and Stability Samples.
  • Performed routine cell-based potency testing for in process, final product, and stability samples.
  • Tested API for stability samples, Release, In Process, and Raw Materials.
  • Performed standard solutions required for testing finished products, in-process, and stability samples.
  • Tested real-time stability samples for ~8 different studies to determine extended expiration dating.
  • Followed protocols and test methods for the analysis of release and stability samples.
  • Tested proteins, in-process, release, and stability samples for multiple clients.
  • Performed testing for raw materials, in-process, finished product and stability samples.
  • Performed Related Compounds Testing for Finished Product including Stability samples by UPLC.
  • Perform testing on stability samples for in-house products and products from Europe.

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8. Hplc

high Demand
Here's how Hplc is used in Quality Control Analyst jobs:
  • Performed HPLC/GC/wet chemistry analysis on raw materials and finished goods used in the quality process of making agricultural chemicals.
  • Received Empower software certification for methods and analysis of data using Waters HPLC
  • Assisted in troubleshooting and optimizing HPLC methods and investigated out-of-specification results.
  • Maintained and calibrated dissolution apparatus and HPLC systems.
  • Performed product stability analyses using established HPLC methods.
  • Worked on special projects such as equipment calibration (HPLC and Dissolution Baths) and method development, validation and transfer.
  • Acquired proficiency in wet chemical analysis & instrumental techniques (including AA, Lambda 3 Spectrometer, GC, & HPLC)
  • Developed QC test SOP s, an Annual HPLC Instrument PQ SOP, and an Electronic Data File Archiving Procedure.
  • Performed HPLC, GC, IR, UV, and wet chemistry analyses of in-process and finished product veterinary pharmaceuticals.
  • Performed an extensive amount of quality control testing such as pH/water content/mixing of dermatological products with emphasis on HPLC testing.
  • Preformed pH and osmosis testing, conductivity, HPLC runs, SDS-Page, environmental monitoring, and cell viability studies.
  • Performed determination of assays on raw materials, in-process and finished products, product stability and proficiency using HPLC.
  • Configured LIMS system to meet product specification, helped with ANRESCO HPLC lab supporting analysis of sucrose and protein.
  • Perform reagent qualification testing for reagents and/or standards to be used in HPLC, PCR, and ELISA assays.
  • Monitored container-closure, fall back, accelerated and long-term stability parameters using HPLC, MS prior to product release.
  • Developed HPLC method validations for the release and stability testing of the company's products and raw materials.
  • Performed Quantitative and Qualitative tests for the analysis of raw materials and finished products using HPLC, FTIR.
  • Prepare samples for, and run Vitamin E analyses on HPLC, using Atlas remote instrument management software.
  • Performed HPLC on raw materials and final container samples for total protein and concentration and desalting analysis.
  • Utilized GC, HPLC, UV spectroscopy, TLC, dissolution and wet chemistry equipment for assays.

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9. Test Cases

high Demand
Here's how Test Cases is used in Quality Control Analyst jobs:
  • Reviewed and analyzed Business requirement documents, Technical specification and documented test cases.
  • Developed and executed test cases for existing software and software under development.
  • Analyzed system specification and developed Test Cases for System and Integration Testing.
  • Lead Professional Reviewed software requirements, specifications, and other design documents for Blood Bank System to execute effective test cases.
  • Develop the test scenarios and test cases for verifying that everything is working as designed according to the proposed design documentation.
  • Drafted test cases and QTP-Quick Test Professional templates to fill out identified gaps resulting in increased performance and minimizing production issues.
  • Analyzed new project impact to Regression test bed and updated existing scripts and/or created new test cases to incorporate the changes.
  • Develop and document test cases and other test artifacts such as test data, data validation, and automated scripts.
  • Executed test cases, analyzed results, reported deviations, identified trends and communicated final testing results to business clients.
  • Executed the test cases in Quality Center, tracked the defects and coordinated with the developers to fix the defects.
  • Created, maintained, and tracked test cases using the QUACC (Quality Assurance Control and Compliance) tool.
  • Used Quality Center as repository for design test cases, Execute test cases, Bug tracking and reporting.
  • Recorded the Test cases using Automation tool QTP and checked the functionality of the application for every release.
  • Created test cases, prepared Test Strategy Plan documents and conducted Verify Product Deliverable meetings with project team.
  • Designed, implemented, and executed test cases enabling rapid deployment of the company's first web-based front-end.
  • Developed a matrix tool for the analysis of regression test bed to locate deficiencies in automated test cases.
  • Created use cases, test plans, test scenarios, and test cases based on the defined requirements.
  • Created and executed test cases as part of quality control efforts for a large scale compliance software project.
  • Performed System and Integration testing by executing test cases by using Microsoft Test Manager (MTM).
  • Documented test cases and generated reports using Mercury Quality Center (Test Director) and Business Objects.

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10. PH Meter

high Demand
Here's how PH Meter is used in Quality Control Analyst jobs:
  • Operated various technical laboratory instruments such as: pH Meter, Conductivity Meter, UV Spectrometer and HPLC.
  • Operated and maintained laboratory equipment including vacuum oven, autoclave, pH meters, and balances.
  • Maintained and calibrated lab instrumentation (i.e., pH meter, balance, etc).
  • Calibrated and operate of instruments like pH meter, balance weights, and pipettes.
  • Maintained and operated lab instrumentation, including pH meters, pipettes and balances.
  • Performed leak and stability tests which utilized pH meters and spectrophotometers.
  • Maintained equipment including pH meters and probes, balances, water baths, HPLCs, bio-safety hoods, Milli-Q systems.
  • Calibrated pH meter, analytical balances, and other lab equipment.
  • Analyze raw materials and finished goods using GC, HPLC, Mettler Toledo, pH meter and other analytical instruments.
  • Trained analysts on GMP use of Yokogawa data monitoring systems, spectrophotometers, pH meters, and balances.
  • Performed calibration of pH meter, analytical balance, UV visible spectrophotometer, HPLC and GC.
  • Operated pH Meters, TOC, Viscometers, Karl Fischer and performed titrations.
  • Operate and maintain analytical instrumentation such as pH meters, spectrophotometers, clinical chemistry analyzers, automatic titrators, and centrifuges.
  • Prepared buffers and reagents, Took absorbance on UV VIS Spectrophotometer, Calibration of PH meter, Micropipettes, balance and spectrometry
  • Worked with esters, specific gravity, karl fischer, ph meter, titrations, tested viscosity, filtered samples.

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11. Audit Procedures

high Demand
Here's how Audit Procedures is used in Quality Control Analyst jobs:
  • Wrote/revised business and audit procedures.
  • Enhanced internal audit procedures to ensure compliance to FAA standards.

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12. Uv/Vis

high Demand
Here's how Uv/Vis is used in Quality Control Analyst jobs:
  • Operated and calibrated all Laboratory Instruments including UV/VIS, HPLC etc.
  • Test in-process, drug substance, and finished goods utilizing HPLCs, UV/VIS, and prep HPLC.
  • Performed UV/Vis and wet chemical analysis to support process control.
  • Determined protein concentration (A280) by UV/VIS spectrophotometry.
  • Performed Dissolution, Assay, CU Test by UV/Vis.
  • Operated a UV/Vis to analyze enzyme activity.
  • Use and knowledge of equipments like HPLC, UV/VIS, Karl Fisher, Dissolution Baths, pH meter.
  • Conduct testing on in-process bulk reactions for production using HPLC and uv/vis.
  • Evaluated production control for over-the-counter and prescription medications Applied various analytical methods including: GMP, SOP, HPLC, UV/Vis.

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13. Cgmp Regulations

high Demand
Here's how Cgmp Regulations is used in Quality Control Analyst jobs:
  • Experience in reviewing manufacturing formulation batch production records to ensure compliance with specification and cGMP regulations.
  • Recorded, analyzed and maintained all testing data as well as ensure document quality and accuracy under cGMP regulations.
  • Followed the cGMP regulations and performed Quality Control (QC) testing on tablets, capsules.
  • Performed moisture analysis and prepared solutions, standards, mobile phases under cGMP regulations.
  • Train analysts on assays, instrument/lab maintenance activities, and cGMP regulations.
  • Perform routine analytical testing of biological drug products according to cGMP regulations.
  • Support for manufacturing with in process analytical testing, EM data trending, and OOS investigations with adherence to cGMP regulations.
  • Maintained accurate and concurrent testing records and ensure compliance with company SOPs and specifications, USDA and cGMP regulations.
  • Follow cGMP regulations, SOPs and other required document.
  • Reviewed and Revised SOPs according to cGMP regulations.
  • Created, revised, and reviewed hundreds of SOPs through a change control documentsystem to comply with cGMP regulations and guidelines.

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14. FDA

high Demand
Here's how FDA is used in Quality Control Analyst jobs:
  • Supported testing operations in a 20-person Chemical Laboratory, monitoring production quality for 3 FDA approved products already in production.
  • Provide microbiological and regulatory expertise to the Quality and Operations groups regarding FDA and European Union regulatory expectations.
  • Evaluated patient care products within manufacturing department that enabled FDA approval for new product developments.
  • Developed reserve sample program of storage, inspection and documentation for clients following FDA requirements
  • Performed and documented testing in FDA-regulated environment for global manufacturer of therapeutic plasma proteins.
  • Performed updates on laboratory Standard Operating Procedures to reflect improvement and FDA guidelines.
  • Lead the implementation of a new FDA regulated product-labeling process into manufacturing.
  • Implemented FDA regulatory practices for production and quality control.
  • Aided in contamination investigations and FDA audits.
  • Documented test results with minimum errors in accordance with GMP, GLP's, and Good documentation Practices and FDA regulations.
  • Analyzed and performed quality control evaluations, according to FDA or OECD regulations, on studies, validations and reports.
  • Approved testing results, Manufacturing batch records and certificate of analysis in compliance with the company standards and FDA requirements.
  • Monitored all quality assurance animal testing for compliance with FDA, USDA, GLP, and USP guidelines and requirements.
  • Review and compile testing data received from the QC Marketed Labs and evaluate compliance to appropriate FDA standards and procedures.
  • Prepared for FDA and IMB audits; assessed Laboratory and Manufacturing areas per IMB and FDA inspections to ensure compliance.
  • Prepared submissions to the FDA and other regulatory agencies, based on information collected from various departments within the company.
  • Complied with current Good Manufacturing Practices as required by FDA and other regulatory agencies, and followed safety procedures.
  • Impacted mission critical operations across numerous departments, thousands of global users, and corporate compliance with FDA regulations.
  • Observed, recorded, maintained, and performed data analysis according to Good Laboratory Practices and within FDA guidelines.
  • Identified test objectives according to Merck web standard and FDA 21 CFR part 11 business requirements after business analysis.

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15. Lims

average Demand
Here's how Lims is used in Quality Control Analyst jobs:
  • Provided microbiological trending data from the Laboratory Information Management System (LIMS) for support of investigations and regulatory agency audits.
  • Assessed modifications to LIMS functionality including programmatic design, system configuration, and metadata changes.
  • Helped identify LIMS user requirements for sample processing and instrument maintenance tracking.
  • Performed facility water sampling and entered data into LIMS database.
  • Created and revised LIMS Stability protocols and product specifications.
  • Participate in LIMS feasibility project.
  • Perform troubleshooting of LIMS issues, and escalate any issues to IT that cannot be resolved as a LIMS Admin.
  • Perform routine analyses of samples; process, analyze, and report data via Laboratory Information Management System (LIMS).
  • Performed final approval of exception documents, test data, and release functions in LIMS or other computerized systems.
  • Review test data to ensure results meet all specifications and input data into the QC LIMS system and MANMAN.
  • Qualified on Empower 3 Data Acquisition System, Laboratory Information Management System (LIMS) and Empower Interface.
  • Experienced with QMS software such as Track Wise, laboratory data management software LIMS and Enterprise software SAP.
  • Supported general laboratory activities like reagent preparation, routine equipment maintenance, data entry and review in LIMS.
  • Create, modify and maintain the static data objects that are used to support more complex LIMS builds.
  • Implemented several simplification projects as a LIMS admin that saved analysts time when testing and logging in samples.
  • Utilized quality systems such as of computer systems such as GLIMS, JLL, MAXIMO and ATLAS.
  • Collect the data, enter the result in the LIMS system and file all the testing documentation.
  • Worked on LIMS assay grids regarding assay chronology, permissions, and sample storage and expiry dates.
  • Record and track data in LIMS and QUMAS; calibrate and maintain lab instruments / equipment.
  • Collaborated with SAP experts on the design, and implementation of the SAP QM LIMS system.

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16. GC

average Demand
Here's how GC is used in Quality Control Analyst jobs:
  • Confirmed blend composition via GC ensuring outgoing products met required specifications.
  • Developed and implemented a training program for GC instrumentation.
  • Developed a method for residual solvents by GC and performed an investigation of raw materials and finished products for residual solvents.
  • Performed and developed GC qualitative assays for final approval of products for purity and dispatch.
  • Determined Fatty Acid Profile (FAP) using GC-FID for tropical oils and fats.
  • Conduct analysis for pesticides utilizing GC/MS on all incoming raw materials.
  • Performed analysis of the different propellants and solvents on GC.
  • Analyzed gas samples using HPGC (Hewlett Packard 5890A).
  • Analyzed water and soil samples for Gasoline and Petroleum Range Organics (GRO/PVOC) and VOCs using Purge-and-Trap/GC and GC-MS.
  • Conducted training sessions to Lab Technicians on modern chromatographic techniques LCMS and GCMS.
  • Performed GC on various wastewater samples and collected and retained samples of PAP.
  • Operated the Gas Chromatograph (GC) for identification of microbial contaminates.
  • Worked on various projects including Multinational Geospatial Co-production Program (MGCP).
  • Worked with UV/IR, GC, and Co-Oximeter and Nova-stat profiler.
  • Experienced composing and revision of SOPs compliant with GMP/GCP.
  • Devised and conducted experiments for determining & improving limits of detection Increased productivity in the lab Trouble-shooting GC Instrument
  • Analyzed daily incoming/outgoing samples using the following instrumentation: Karl Fisher, densitometer, viscometer, LC and GC instruments.
  • Sample prep for GC analyses, and the use and operation of GCs equipped with Chemstation software.
  • Helped with the troubleshooting, use, and operation of GCs equipped with Chemstation software.
  • Worked with GC, LC, UV-Vis and other analytical lab instruments.

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17. Bioburden

average Demand
Here's how Bioburden is used in Quality Control Analyst jobs:
  • Executed method validation of pour plate method for bioburden microbial limit testing, improving upstream manufacturing processes.
  • Performed component and finished product microbiological testing (bioburden, sterility, antibiotic potency).
  • Analyzed in-process samples for bioburden, cell culture purity and microbial identification.
  • Perform testing of critical biological process for Identification and In-process bioburden.
  • Performed sterility and bioburden testing, plate reading and microbiological identifications.
  • Performed bioburden testing by membrane filtration.
  • Conducted bioburden and conductivity testing.
  • Collected water samples from WFI, clean steam, and RODI water systems and put those samples through bioburden testing.
  • Perform environmental monitoring including but not limited to bioburdens, viable airborne particle counts, and microbiological air sampling.
  • Read EM plates and Bioburden plates, and track various projects such as investigations and alerts weekly.
  • Perform IPB (In Process Bioburden) testing of plasma samples, and raw materials.
  • Perform EM, Conductivity, and Bioburden testing for DIH20, in-process and finished products.
  • Conduct Bioburden testing (RO/DI) to determine the sterility of purified water systems.
  • Run TOC, conductivity, chlorides, bioburdens, and pH on water daily.
  • Authored Validation Reports for Sterility, Bioburden, Extrusion, HIAC Test Methods.
  • Performed Bioburden, TOC, LAL, BI, Conductivity and pH assays.
  • Performed Bioburden Testing of WFI water, raw materials and finished products.
  • BET and bioburden testing of API, in-process, and finished product.
  • Conducted routine assays, including bioburden, TOC, pH and conductivity.
  • Performed Bioburden Testing of In-process products, buffers, and water.

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18. Final Product

average Demand
Here's how Final Product is used in Quality Control Analyst jobs:
  • Performed and reported qualitative and quantitative analysis of raw materials and final products for quality control.
  • Facilitate timely release of manufactured products, by performing microbial assays of in-process and final products.
  • Conducted critical chemistry analysis of raw materials and final products for the pharmaceutical industry.
  • Performed final product identity testing.
  • Evaluated final product, intermediate products, raw materials, and production facility samples to ensure compliance with industry quality standards.
  • Performed routine chemical analysis on raw materials, in-process, and final products to determine if sample met quality specifications.
  • Analyzed the samples from research and development for purity and stability for further use of the intermediates and final products.
  • Performed quality control testing of in process, final product and stability sample testing in a GMP compliant manner.
  • Analyzed raw incoming materials using a variety of methods including FTIR as well as quality checks of final products.
  • Performed operations necessary for Quality Testing of raw materials, in-process and final products in accordance with SOP's.
  • Analyzed raw material, by product for process and final product in the elaboration of precooked corn flour.
  • Participated in construction and maintenance of SOP, BSE-TSE and MSDS; Issued CoA on qualified final products.
  • Reviewed quality control testing documentation for release of cell banks, intermediates, in-process and final product material.
  • Perform analysis of ink products throughout the production process which includes release of final product and sensory testing.
  • Performed methods in the analysis of in-process and final product, raw materials, and water purity.
  • Monitor, measure and implement quality changes to manufacturing process of converting raw materials into final product.
  • Tested wide range of bulk pharmaceutical drugs at raw material, intermediate, and final product stages.
  • Test samples of raw materials, in process samples and final products to the specifications designated.
  • Collaborate with Quality Assurance, Research and Development, and Production from rough draft to final product
  • Perform critical chemical and physical analyses on raw materials, initial, in-process and final products.

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19. Endotoxin

average Demand
Here's how Endotoxin is used in Quality Control Analyst jobs:
  • Executed EndotoxinBe consistent with upper and lower case terms!
  • Perform inhibition enhancement testing for endotoxin validation sample.
  • Authored endotoxin and cell viability method validation protocols.
  • Conducted microbial and endotoxin testing on environmental, in process, bulk and final vial samples.
  • Performed ELISA, BCA total protein assay for Cleaning Validation, Endotoxin and HPLC analysis.
  • Performed PCR, protein expression and purification, assay to determine endotoxin level in drug.
  • Provide rapid results for cleaning validation protocols for Endotoxin, TOC and Conductivity testing.
  • Subject Matter Expert (SME) in Endotoxin, Conductivity, and Nitrate testing.
  • Performed STAT endotoxin tests on water, buffers and drug products to support production.
  • Executed pour plate, membrane filtration, conductivity, TOC, & endotoxin testing.
  • Lead a validation project to determine the endotoxin for samples tested in the facility.
  • Analyzed drug products, water and buffer solution samples for the presence of Endotoxins.
  • Observed Growth Promotion, Endotoxin, Identifying Molds, and Nitrates Testing.
  • Trained to perform Kinetic LAL and Gel Clot analysis for endotoxin determination.
  • Performed the qualification of incoming Endotoxin, media and organism supplies.
  • Performed endotoxin, conductivity and TOC for the water systems.
  • Perform LAL/Endotoxin assay on routine USP water and buffers.
  • Conducted Endotoxin studies in conjunction with a dual-company request.
  • Focus assessments on Sterility USP and Endotoxin USP.
  • Assisted in environmental monitoring and water sampling procedures, testing procedures (bioburden, endotoxin), and validation protocol executions.

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20. Data Entry

average Demand
Here's how Data Entry is used in Quality Control Analyst jobs:
  • Execute numerous administrative duties including operating switchboard, filing, analyzing documents, and data entry.
  • Performed routine environmental monitoring, data entry, review, and document revisions verification.
  • Assisted occasionally with review/verification of data entry and stability study set ups.
  • Verified and approved data entry for automation process of data analysts.
  • Handled data entry duties and demonstrated extremely high productivity and accuracy.
  • Perform daily data entry of departmental information into reporting forms.
  • Documented analysis results and completed SAP application data entry.
  • Returned all uncorrected data entry to analyst for corrections.
  • Developed and implemented a data entry database.
  • Review accuracy of laboratory data entry.
  • Performed daily audits for our platinum clients and monthly audits of the data entry operators and made recommendations for quality improvement.
  • Performed in-process, release & stability testing; data entry, analysis, and prepared data summaries/reports for various clients.
  • Re-established internal service levels and production standards for the Data Processing department resulting in 0% data entry errors.
  • Performed clerical duties including phone, fax, e-mail, filing, data entry, and order checking.
  • Operated and maintained database system, including data entry, report generation, data archives, and billing.
  • Sample preparation, sample analysis, calculating data, data entry, validation data, instruments validations.
  • Analyze production batches and assist with data entry, daily activity log, and incident updates.
  • Provided feedback to clerical and data entry employees regarding work processes, quality concerns, etc.
  • Finished product spoilage report and data entry for later sales, inventory and accounting purposes.
  • Review data entry reports for any errors in consumer records and make corrections if needed.

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21. Validation Protocols

average Demand
Here's how Validation Protocols is used in Quality Control Analyst jobs:
  • Support cleaning verification and validation by drafting validation protocols for GMP manufacturing equipment Maintained inventory and log books according to CGMP.
  • Review and approval of QC data, development of microbiological assays and validation protocols.
  • Authored and revised Standard Operating Procedures, Validation Protocols, Stability Protocols and Forms.
  • Drafted and finalized standard operating procedures, qualifications, validation protocols and reports.
  • Write validation protocols, execute experiments and write validation reports based on results.
  • Authored and executed validation protocols for plate-based enzyme activity testing.
  • Authored and edited standard operating procedures for cleaning validation protocols.
  • Participate in execution of Method Validation Protocols and Technology Transfer.
  • Execute qualification and validation protocols to support Assay Validation.
  • Execute Laboratory Validation Protocols and Method Development as needed.
  • Create and execute Validation protocols for incubators and refrigerators.
  • Executed validation protocols for environmental monitoring in manufacturing ambient.
  • Assist in writing qualification and validation protocols and reports.
  • Prepared validation protocols, performed experiments and prepared reports.
  • Executed validation protocols for a new laboratory equipment.
  • Executed validation protocols on new and existing methods.
  • Authored and executed equipment and method validation protocols.
  • Execute method transfers and method validation protocols.
  • Authored method validation protocols and summary reports.
  • Reviewed and executed validation protocols and reports.

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22. ISO

average Demand
Here's how ISO is used in Quality Control Analyst jobs:
  • Conduct discrepancy documentation and electronically input them onto spreadsheets as to inform direct supervisor for presentation to the Operations Executive Manager.
  • Served as a liaison between QC and Manufacturing by communicating test results and organizing testing/retesting schedules around production schedule.
  • Performed laboratory analysis for finish products, raw materials and active ingredients under the direction of the laboratory supervisor.
  • Organized and compiled data, assist in the analysis of data by statistical procedures as requested by manager/supervisor.
  • Serve as quality liaison during third party audit visits or external monitoring organizations and/or customer evaluation compliance call.
  • Notified supervisor and specified personnel of deviations from specifications, machine malfunctions and need for equipment maintenance.
  • Coordinated liaison activities between several client companies as well as internally to ensure quality and accuracy.
  • Requested by management to assume temporary supervisor role in Commercial Paper Department during critical audit period.
  • Characterize bacterial and fungal isolates, execute test method validations, and assist with investigations.
  • Performed various supervisory responsibilities as well as performing Software Testing on various internal Software products.
  • Provided quality control by assigning and verifying specific roles and permissions to commissioners and supervisors.
  • Provided advisory and training to laboratory analysts on a daily basis in a lead capacity.
  • Isolated, separated and re-evaluated materials deemed to be non-compliant with regards to established specification.
  • Team Mentor-assisting supervisor with special projects, Programs department representative, Center of Excellence representative.
  • Worked closely with telesales supervisors to ensure telesales agents were meeting strict quality standards.
  • Promoted to Production supervisor in which I was responsible for approximately 20 chemical operators.
  • Second and third Shift Supervisor for a manufacturer of specialty chemicals with industrial applications.
  • Hand selected by senior supervisors to translate critical documents for time sensitive operations.
  • Assisted supervisors in monitoring interviewers, develop/improve training documentation, providing written/verbal critique.
  • Prepare full research reports including company history and industry comparison for management review.

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23. Ftir

average Demand
Here's how Ftir is used in Quality Control Analyst jobs:
  • Maintained and calibrated all QC laboratory equipment to include NMR, XRF, FTIR, and MP600 Melt Index instruments.
  • Performed sampling and ID testing of incoming GMP raw materials, including wet chemical and FTIR analysis.
  • Finished Product Fourier Transform Infrared Spectroscopy (FTIR) analysis.
  • Perform testing on activated polystyrene devices using FTIR including microscopic and Attenuated Total Reflectance (ATR).
  • Analyzed compounds using FTIR to determine chemical and physical properties.
  • Worked on FTIR for identification of raw materials for qualitative analysis.

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24. Chromatography

average Demand
Here's how Chromatography is used in Quality Control Analyst jobs:
  • Assisted in troubleshooting and maintenance issues regarding software, instrumentation, system suitability, column, integration and general chromatography questions.
  • Prepare process buffers needed to support chromatography and ultra filtration steps to manufacture pharmaceutics.
  • Prepared research study on Comprehensive Two-Dimensional Ultrahigh-Pressure Liquid Chromatography for Separations of Polymers.
  • Analyzed quantitatively amount of raw chemical concentrations using Gas Chromatography/ Mass Spectrometer.
  • Experienced data processing, review and management in chromatography and other platforms.
  • Perform chemical requirements and chromatography of in-process and finished products.
  • Employed affinity chromatography methods for biological commercial product.
  • Performed separation of solvent properties using chromatography techniques.
  • Determined chemical concentrations using Gas Chromatography/ Mass Spectrometer.
  • Water analysis solutions using ion chromatography.
  • Purified gp160 antigen using pressure liquid chromatography
  • Gas chromatography, C6+ and C9+, BTU / process gas analysis, trouble shooting and calibration of GC / gas analyzers
  • Supported manufacturing through in-process testing, including size exclusion high performance liquid chromatography, ion exchange and SDS PAGE.
  • Well-versed in X-ray florescence, ICP, gel permeation/gas chromatography, TOC analysis, and infrared testing.
  • Collect and perform Raw Material and Gas Chromatography testing for Alcohol drops throughout the facility.
  • Performed various quality control tests including stability testing, ELISA assays, and Gas Chromatography.
  • Analyzed flavors and fragrances samples using a Gas chromatography-mass spectroscopy (GC-MS) equipment.
  • Monitored and assisted with questions from Internal Audit in regard to Chromatography area.
  • Used Gas Chromatography in the detection of ethanol, 1-propanol.
  • Finished Product Thin Layer Chromatography (TLC) analysis.

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25. QA

average Demand
Here's how QA is used in Quality Control Analyst jobs:
  • Managed all phases of the administrative computer center - hardware/software acquisition/testing & QA/implementation/disposal, human resource (including conflict) management.
  • Conducted laboratory analysis, instrument maintenance, instrument calibration and QA/QC compliance.
  • Performed data verification of packaging components for QA approval.
  • Coordinate with QA for documentation development.
  • Gather water, steam and compressed gas samples from manufacturing and utilities area to perform microbiological tests within the QA lab.
  • Involved in a TQM Process Improvement Team to streamline the collection of Army QA and QC inspection data within the department.
  • Experienced in initiating, authoring, and working with QA-Compliance to close Deviations, Change Controls, and Laboratory Investigation Reports.
  • Work with both operational and QC/QA audit management staff to review system and technical changes for system enhancements and upgrades.
  • Assist the QA team to obtain a QP declaration within the European Union for the purpose of pharmaceutical clinical trials.
  • Reviewed existing QA/QC for the Department's FOIA operations and suggest improvements for best practices within the FOIA section.
  • Drive product quality, user experience and client satisfaction through QA processes and systems for custom Rich Media campaigns.
  • Work closely with development team to create and QA new tools to improve accuracy and efficiency of data loaded.
  • Revised existing departmental written procedures for FOIA & PA processing to incorporate improved QA/QC practices and other process improvements.
  • Provide regular status report to QA Lead and Project management, updating tasks and tasks estimates, as necessary.
  • Installed and set up Mercury Quality Center, QA error tracking and documentation tool for entire portal group.
  • Collaborate with developers and FPS QA team members to identify defects and validate bug fixes before each release.
  • Maintained and updated QA systems (holds, incoming inspections, weight control, etc.).
  • Assisted in developing and improving QA programs and procedures, as well as in new product development.
  • Pipe Production: QAQC analysis on composite pipes to ensure that they fall within the required specifications.
  • Send out QA exceptions to Operations and provide response once exceptions have been satisfactorily addressed by Operations.

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26. Microbiology

average Demand
Here's how Microbiology is used in Quality Control Analyst jobs:
  • Consulted with sensory, microbiology and packaging Subject Matter Experts to verify information regarding brand label and private label products.
  • Performed critical media preparation at Microbiology Laboratory, analyzed microbial samples and prepared specific dilution concentrations for its posterior analysis.
  • Presented Power Point presentation of Overview of Microbiology Procedures and corrective actions for deviations or product non-conformance.
  • Performed sterilization of laboratory equipment, cleaned and disinfected equipment, work area and Microbiology aseptic room.
  • Evaluated, purchased and validated/qualified laboratory equipment for Microbiology, Biochemistry, Chemistry and Raw Material Labs.
  • Performed routine microbiology task such as media qualification, organism qualification, reads, and microbial identification.
  • Planned, prioritized, conducted data trending, ordered laboratory supplies and scheduled workloads for microbiology analysts.
  • Review static and dynamic environmental monitoring records including personnel monitoring for the microbiology quality control department.
  • Performed final review of environmental monitoring data that was generated by Quality Control Microbiology and Manufacturing.
  • Maximized operational efficiency of Quality Control, Microbiology by streamlining testing preparations and improving sampling procedures.
  • Presented microbiology deviations at daily management meetings and devised solutions to prevent future occurrences.
  • Trained new microbiologists and assessed progression in clean room sampling and microbiology laboratory techniques.
  • Managed inventory of consumables, media, and testing organisms in QC Microbiology laboratory.
  • Performed microbiology quality control analysis of raw materials and final medication products.
  • Validated culture media for microbiology analysis, minimizing the occurrence of contamination.
  • Obtained microbiology techniques like media preparation, identification of bacteria and gram-staining.
  • Completed QC testing in both Chemistry and Microbiology labs on anti-coagulant pharmaceutical.
  • Conducted planning and performing of comprehensive microbiology tests and provided detailed updates.
  • Developed operation and maintenance procedures for all microbiology instruments / equipment.
  • Lead analyst for microbiology, micro containment and tissue culture laboratory.

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27. Customer Service

average Demand
Here's how Customer Service is used in Quality Control Analyst jobs:
  • Promoted to a Quality Control Analyst position within two months of hire by consistently demonstrating outstanding customer service expertise.
  • Resolved customer service issues related to quality control by investigating problems and providing solutions resulting in customer satisfaction.
  • Provide exceptional customer service by registering all the measurements necessaries of FOUPS in a semiconductor environment.
  • Revised and implemented policy, procedures and training materials to maximize efficiency and customer service.
  • Identified training opportunities by reporting production errors while monitoring inbound and outbound customer service calls.
  • Communicate with engineering, operations, and project management teams to improve SolarCity customer service.
  • Use customer service experience to assess existing practices and procedures for process improvement opportunities.
  • Recognized by management on numerous occasions for a strong commitment to excellent customer service.
  • Developed protocols for customer service personnel to ensure adherence to quality service measures.
  • Performed quality control functions for incoming claims and provided exceptional customer service.
  • Performed detailed auditing of all transactions processed by customer service reps.
  • Promoted from Customer Service Associate to Customer Service Quality Control Analyst.
  • Provided technical support and consulting support for Customer Service.
  • Performed quality audits on various customer service processes.
  • Managed daily statistics for customer service center.
  • Trained Customer Service Representatives and Underwriting Assistants.
  • Provided customer service for Medicare recipients.
  • Certificate of Stellar Customer Service completion.
  • Create PP based on own findings, to compare how competitors handle Customer Service issues, cost, logistics, etc.
  • Provide Customer service to our internal/external clients as it pertains to searches, reports, status, invoicing and technical errors.

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28. Elisa

average Demand
Here's how Elisa is used in Quality Control Analyst jobs:
  • Perform biological and chemical assays - ELISA, tissue culture, cell-based assays and enzyme assays.
  • Carried out and reported data from ELISA release assays for Quality Control using established GMP protocols.
  • Transferred and qualified new ELISA assays for product testing from the Research and Development groups.
  • Performed stability testing on different reagents in a testing kit using ELISA assay.
  • Involved in validation and verification of automated system for ELISA and DNA extraction.
  • Performed CV testing on all in house manufactured ELISA plates for clinical testing.
  • Performed Elisa Assay, to measure the concentration of IgG of Antibodies.
  • Managed the validation of Quality Control ELISA data spreadsheets and associated documents.
  • Studied the binding affinity of several drugs using ELISA and Dot Blots.
  • Performed the ROS biological assay and residual CHO Host Cell Protein ELISA.
  • Performed cell-based ELISA assay (VEGF) for clinical trials.
  • Coated 96-well and 384 ELISA plates from purified selective antigens.
  • Experience in transferring ELISA procedures and executing new protocols.
  • Participated in the validation of the CHO ELISA assay.
  • Qualified critical reagents for various ELISA methods.
  • Decreased TAT of ELISA assays 2-fold.
  • Conducted ELISA experiments on serum samples.
  • Experienced in automated ELISA assays.
  • Perform Mouse IgG1 and Rat IgG2b ELISA assays.
  • Conducted ELISA analysis of international aeroallergen samples.

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29. Wet Chemistry

average Demand
Here's how Wet Chemistry is used in Quality Control Analyst jobs:
  • Analyzed and identify the physical composition of compounds and chemical properties of samples using qualitative analysis and wet chemistry method.
  • Worked in an environment utilizing basic wet chemistry techniques.
  • Performed wet chemistry and general testing on incoming raw materials according to defined in-house methods, and USP guidelines.
  • Performed wet chemistry tests as: TLC, solubility, acidity-alkalinity, ROI, Heavy Metals, LOD.
  • Experience in wet chemistry techniques such as KFR technique for the identification and water content.
  • Utilize wet chemistry techniques to quantify Oxidant, Calcium and Sulfur Dioxide levels.
  • Worked with a variety of wet chemistry and top-of-the line instrumentation.EXPERIENCE, CTD.
  • Analyze UF6 using ICP-MS, AA and wet chemistry methods for purity.
  • Perform wet chemistry tests, comply with good housekeeping and safety practices.
  • Demonstrate fundamental physical, wet chemistry, and instrument analyses techniques.
  • Perform various wet chemistry tests on a variety of instruments.
  • Performed wet chemistry methods in testing finished and bulk products.
  • Wet chemistry techniques, including heavy metal and arsenic digestions.
  • Performed tests and assays by wet chemistry and instrumental techniques.
  • Performed wet chemistry and biological assays for in-process samples.
  • Conduct wet chemistry per USP and EP methods.
  • Performed wet chemistry test on water samples.
  • Use wet chemistry methods to test samples.
  • Develop and maintain wet chemistry techniques.
  • Used classical wet chemistry methods.

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30. GLP

low Demand
Here's how GLP is used in Quality Control Analyst jobs:
  • Performed QC related audits of GMP documentation to include: logbooks, laboratory notebooks, and completed GMP/GLP assay specific documentation.
  • Reviewed all products made from proper specification as required by SOP's into GMP and GLP before getting approved for use.
  • Performed biological quality control analysis under Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) standards.
  • Performed chemical and microbiological testing on over-the-counter and personal care products using GMP's and GLP's.
  • Performed and maintained GMP/GLP documentation by authoring and continuously revising all equipment and assay system SOP's.
  • Comply with GLP but is not limited to laboratory notebooks Smart Lab (CIMS) and LMES.
  • Approve QC laboratory data ensuring correct GLP and GMP guidelines are followed and validated procedures are utilized.
  • Maintain documentation for all steps of assay processes to conform to GLP and GMP compliance requirements.
  • Undertake the routine testing of different finished products, intermediates and raw materials under GMP/GLP guidelines.
  • Follow safety guidelines required as per SOP's before performing testing in a GLP environment.
  • Gathered data and prepared reports for approval of incoming materials under GLP and GMP compliance.
  • Disciplined in strict government regulations and company policies in a GMP and GLP environment.
  • Followed company SOP's in day to day activities, also maintained GMP/GLP compliance.
  • Maintain a GMP and GLP compliant work environment, including a laboratory notebook.
  • Based on current GMP, GLP, MSDS, and safety regulations.
  • Performed duties in a GMP, GLP, and ISO certified environment.
  • Developed and improved GMP/GLP lab methods and revised associated SOP documents.
  • Performed all assays in accordance with SOP and GMP/GLP regulations.
  • Design and execute experiments on new formulations following GLP.
  • Performed validation of QC GMP/GLP cell-based assay systems.

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31. Capa

low Demand
Here's how Capa is used in Quality Control Analyst jobs:
  • Developed manufacturing process capability assessments.
  • Supported laboratory investigations, Out-of-Specification (OOS) and exceptions reporting and CAPA investigations by providing technical expertise and input.
  • Performed and presented digital microbiological photography of bacterial and fungal recoveries in support of accurate diagnosis and investigative CAPA reports.
  • Led extensive system capabilities test to demonstrate feasibility to effectively measure and report parameters associated with high interest signals.
  • Identified discrepancies; participated in quality investigations and CAPA (corrective actions preventive actions) initiatives as needed.
  • Advance and accelerate company's quality improvements from corrective action to process improvement and capability development.
  • Improved call center functionality and service capacity by resolving escalated customer complaints professionally and efficiently.
  • Perform Corrective action/preventive action (CAPA) management and non-conformance management processes.
  • Evaluated legitimacy of data while exercising good judgment on repayment capacity.
  • Manage data reporting infrastructure and identify future enhancements or capabilities.
  • Compare production line capabilities and ensure product quality consistency.
  • Provide support to laboratory investigations and CAPA's resolutions.
  • Demonstrated capacity to function independently and productively.
  • Compiled demonstrations of capability for each analyst.
  • Initiated deviations and CAPA investigations.
  • Completed all Corrective Action Preventative Action (CAPA), Root Cause Investigations (RCI) and Non-Routine procedure evaluations assigned.
  • Write Deviation and or CAPA in incident of OOS, discrepancies, client complaint, audit or regulatory agency observations.
  • Managed SRS; generated protocols for system functionality and interfaces with Quality Control, CAPA, Reporting and Metrics systems.
  • Involved in all aspects of CAPA s including root cause analysis, and made recommendations to management for corrective actions.
  • Led multiple CAPA Projects that had major impact on improving the quality and efficiency of QC processes.

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32. Preventative Maintenance

low Demand
Here's how Preventative Maintenance is used in Quality Control Analyst jobs:
  • Maintained equipment and laboratory including cleaning, calibration, and scheduling preventative maintenance.
  • Performed routine and non-routine preventative maintenance and calibration of laboratory equipment.
  • Maintain database of QC equipment preventative maintenance and calibration schedule.
  • Calibrated and performed preventative maintenance on the MilkoScan FT2 analyzer.
  • Perform cleaning / preventative maintenance on laboratory equipment as required.
  • Perform preventative maintenance on all quality control chemistry equipment.
  • Maintained lab equipment for calibrations and preventative maintenance.
  • Perform cleaning and preventative maintenance on equipment.
  • Perform lab instrumentation calibration and preventative maintenance.
  • Perform instrument, laboratory, and facility preventative maintenance, repair, and calibration.
  • Performed preventative maintenance and ordered spares for HPLC systems.
  • Calibrated and performed preventative maintenance on HPLC, spectrophotometry and dissolution instrumentation.
  • General maintenance of lab equipment regarding calibration, certification and preventative maintenance.
  • Key Highlights: Reduced incidents of vehicle down-time and utilized preventative maintenance techniques to minimize or avoid malfunctions in advance.
  • Perform preventative maintenance on complex laboratory equipment and other various lab duties to maintain a cGMP environment.

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33. R

low Demand
Here's how R is used in Quality Control Analyst jobs:
  • Maintained database to reflect quality control outcomes by individual staff and departments and generated written reports for agency management.
  • Review and submit revisions to residential appraisers regarding appraisals written for various lending companies.
  • Performed laboratory testing on finished product, cleaning validation, stability and validation sample.
  • Prepared and conducted internal and external audits and helped prepare for a regulatory inspection.
  • Assess process performance by observation of floor laboratory operations and review of performance data.
  • Designed laboratory, purchased equipment, and calibrated equipment for poly metallic mine.
  • Use sophisticated laboratory instrumentation and computer systems to collect and record data.
  • Evaluate, plan, and implement solutions for laboratory improvement opportunities.
  • Reviewed and approved manufacturing batch records following current GMP documentation guidelines.
  • Provide support of timely execution of the process monitoring quarterly reports.
  • Develop and validate Microsoft Excel Spreadsheet to speed-up the laboratory calculations.
  • Performed laboratory Data Validation, Validation Protocol and Validation Project.
  • Recorded, evaluated, interpreted and summarized technical data independently.
  • Reviewed Cleaning instructions and documentation used in the cleaning activities.
  • Prepared qualification protocols and reports for assignments within QC Laboratory.
  • Conducted physical and chemical tests to address compliance with specifications.
  • Collaborate with associates to improve efficiency, productivity and processes.
  • Trained and practiced standard laboratory procedures within three separate departments.
  • Support establishment of process monitoring parameters and control limits.
  • Collect process-monitoring data and support the assessment of deviations.

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34. LAL

low Demand
Here's how LAL is used in Quality Control Analyst jobs:
  • Experience with EM testing, LAL, water testing, and Raw materials.
  • Worked using sterile technique for LAL assay test under UV light hood.
  • Assisted with investigation with LAL study to identify kit failures.
  • Attended LAL training course at Associates of Cape Cod.
  • Completed microbial limits and LAL for water testing.
  • Conducted in house LAL assays.
  • Performed Quality Control lot release testing which included LAL gel clot, and sterility testing using the Steritest system.
  • Performed pH, Osmolality and visual inspection for raw material testing.
  • Analyzed osmolality, pH and conductivity of broth samples.
  • Conducted and assigned testing for all intermediate testing, including: specific gravity, acid base titration, pH, osmolality.
  • Trained to perform the turbidimetric method using the LAL-5000 or Pyros Kinetic to test daily water samples.
  • Perform routine pH, Appearance, Immunodiffusion, Resin ID, Moisture Content and Osmolality testing.
  • Run samples on the Olympus AU400 analyzer and Osmometer to determine blood chemistry analysis and osmolality.
  • Performed analytical assays like Visual Inspection, pH, Osmolality and Conductivity.
  • Perform Compendial testing such as Appearance, pH, and Osmolality.
  • Analyze for osmolality Analyze for melting point.
  • Trouble shooting: Fixed the Climet programming Talk to vendor to bring the new software for LAL WinKQCL system
  • Conducted UV-Vis spectrophotometry, pH, and osmolality testing of raw materials and products.

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35. OOS

low Demand
Here's how OOS is used in Quality Control Analyst jobs:
  • Function as contact for client communication and management, including stability and release data delivery and AV/OOS notification.
  • Documented SOP, method qualification/validation protocol and report, stability protocol and report, OOS/OOT investigation report.
  • Report OOS (Out of Specification) results and initiates laboratory investigation procedures.
  • Initiate and follow up on OOS investigations*Perform quarterly safety inspections*Proficient in MS Office
  • Reviewed data for compliance with specifications and investigated OOS results.
  • Develop experimental and protocol testing for OOS investigations.
  • Facilitate OOS investigations and report appropriately.
  • Review data and write/direct OOS investigations.
  • Out of Specification (OOS) and root cause analysis * Serve as laboratory representative for projects and cross functional teams
  • Author and collaborate on laboratory investigations for out of specification (OOS), atypical, and invalid results.
  • Created and organized a program within the organization to boost and recognize employee productivity through merits and employee accomplishments.
  • Directed work flow, set priorities and managed OOS reports as a leader on individual high-volume product lines.
  • Investigated and resolved issues related to assay failures (OOS), system deficiencies, and deviations.
  • Assist in the development of an event and re-testing plan does to an OOS result.
  • Performed an OOS investigation for SP2/0 HCP on numerous samples of ch14.18 from multiple lots.
  • Conducted investigations when an Out of Specification (OOS) result was generated.
  • Chaired the writing of all Microbiological OOS (out of specification) investigations.
  • Organized team luncheons each month to help boost morale and encourage team camaraderie.
  • Trained for OOS (Out of specification) investigation and preparing related documents.
  • Review and analyzed data, test reports and conduct OOS results investigations.

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36. FHA

low Demand
Here's how FHA is used in Quality Control Analyst jobs:
  • Performed daily audits of FHA/FNMA/Conventional/Government mortgage loan files.
  • Reviewed and monitored high volume of conventional, FHA, and VA mortgage loans for compliance with industry and federal guidelines.
  • Reviewed legal and regulatory compliance for government programs, including FHA, Fannie Mae, Freddie Mac, VA & USDA.
  • Reviewed loans for conformity according to FHA, VA, FNMA / FHLMC, corporate, and private investor guidelines.
  • Conducted approximately 100 audits reviewing over 500 FHA, VA, and Conventional mortgage loans and avoiding regulatory offenses.
  • Make sure all USPAP, FHA, Fannie Mae and Freddie Mac regulations have been addressed where applicable.
  • Performed income calculations on HARP FHA, VA, FNMA, FHLMC, Private and Proprietary mortgage loans.
  • Review GFE fees in comparison to final HUD-1 documents for conventional, FHA, and VA loans.
  • Perform within Production Quality for Mortgage loans (FHA Loans, HARP, and Conventional).
  • Audit loans for multiple investors including FNMA, FHA, VA, USDA, and Private/Asset.
  • Maintained a continuing working knowledge of FNMA, FHA, and VA QC requirements.
  • Coordinate external audit/regulatory reviews for FHLMC, FNMA, FHA and Private Investors.
  • Identified income and assets for jumbo reviews, Conventional VA, and FHA loans
  • Performed quality analysis checks for revisions on FHA and Conventional Appraisal Reports.
  • Reviewed FHA Loss Mitigation loans for quality and adherence to investor guidelines.
  • Analyzed and reviewed FHA HAMP Modifications for accuracy of the underwriting decision.
  • Review all income documents and calculate income based on FNMA/FHMLC/FHA/VA guidelines.
  • Conduct quality review of FHA loans in default status.
  • Know the Guidelines for FHA and FMHA appraisals.
  • Complete knowledge of FHA regulations.

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37. Growth Promotion

low Demand
Here's how Growth Promotion is used in Quality Control Analyst jobs:
  • Perform growth promotion on all incoming microbiological media to ensure integrity and fit-for-use.
  • Preform growth promotion qualification on all incoming media.
  • Trained on media and microbiological organism growth promotion and sterility testing required to approve new lots of media for lab use.
  • Perform laboratory support functions including: reagent preparation, growth promotion, plate reading, inventory support and data trending.
  • Performed growth promotion testing on media to be used for Environmental Monitoring.
  • Performed gram staining and growth promotion on incoming lots of media.
  • Performed growth promotion of incoming QC media and reagents.
  • Perform the Growth Promotion for media fill.
  • Assisted in Growth Promotion Testing.
  • Completed growth promotion of media, mold identification, gram stains and bacteria identification using Vitek ID system.
  • Performed Growth Promotiontesting on all media produced prior to use in testing.
  • Performed cell-mediated bioassays, including morphology evaluation and growth promotion studies, immunofluorescent and cytochemical staining procedures.
  • Release materials Growth promotion for media Environmental monitoring HPW water sampling Current Good Manufacturing Practices (cGMP)

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38. Ensure Accuracy

low Demand
Here's how Ensure Accuracy is used in Quality Control Analyst jobs:
  • Perform data clean-up activities to improve integrity of database; validated data to ensure accuracy, completeness, and reliability.
  • Provided quality control for processed transactions to ensure accuracy before payments reached the client or their chosen financial institutions.
  • Validated claims for accuracy and completeness, using extensive knowledge of client/agency specifications to ensure accuracy.
  • Evaluate information entered by associates into the system to ensure accuracy and provide quality feedback.
  • Provide support to the Loss Mitigation Underwriting Department to ensure accuracy in modifications.
  • Coordinated with vendors to ensure accuracy of invoices and efficiency of invoice processing.
  • Validated information used in the underwriting review to ensure accuracy and quality.
  • Prepare data and operational reports and schedules to ensure accuracy and efficiency.
  • Audit training and training material to ensure accuracy and effectiveness.
  • Performed verification of employment or deposit to ensure accuracy.
  • Apply mathematical logic principles to ensure accuracy of data.
  • Audited documents to ensure accuracy and validity of information.
  • Reviewed the routine correspondence for adjustments to ensure accuracy.
  • Evaluated results to ensure accuracy and conformance to specifications.
  • Assessed all patient medical documents to ensure accuracy.
  • Reviewed computer-generated matches to ensure accuracy of information.
  • Evaluated transactions to ensure accuracy and completeness.
  • Maintained all operations of company's laboratory; calibrated equipment every 2 weeks to ensure accuracy of tests on all products.
  • Identified control issues to ensure accuracy of calculations and disbursements and ensure internal control standards are met for all clients.
  • Focused on analyzing the work of our client relations representatives to ensure accuracy in the work that was being completed.

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39. Quality Standards

low Demand
Here's how Quality Standards is used in Quality Control Analyst jobs:
  • Conduct assigned number of quality-related reviews of associate's performance, evaluating against established quality standards to ensure proper call handling.
  • Ensured quality standards and compliance to customer and regulatory requirements, and tolerance specifications for the chemical or physical property.
  • Ensured quality products by keeping maintenance and calculations of inventory including measuring whether existing products met set quality standards.
  • Audit existing processes and maintain quality standards by performing dimensional and visual inspections following standardized methods and established techniques.
  • Maintained quality standards of control in order to meet specifications through data collection thereby improving product quality.
  • Conduct in-process and material audit to assure adherence to detailed production procedures and quality standards.
  • Develop an understanding of competing systems and industry data quality standards.
  • Maintain Auditor production and quality standards.
  • Work together to find the cause and the appropriate course of action to take to bring bags back to quality standards.
  • Answered questions from the manufacturing crews to determine if materials to be processed were up to client's quality standards.
  • Observed and scored telephone calls and reviewed team members' work to ensure compliance with quality standards and procedures.
  • Applied quality control analysis from the production line to finished products and ensured production met quality standards.
  • Conducted manual tests on product modules and provided relevant feedback to enhance quality standards of the team.
  • Review of batch tickets to ensure quality standards are met including investigation and correction of discrepancies.
  • Maintain quality standards by making sure all requirements are met in production for consumer safety.
  • Review the current policies and improvise plans to improve upon the existing quality standards.
  • Established quality standards to ensure proper call monitoring techniques and standards are followed.
  • Assisted the FSC with educating the Department regarding the implementation of quality standards.
  • Assess the work of document coders to maintain contractual quality standards for clients.
  • Grade loggers to ensure the quality standards of the company are met.

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40. IR

low Demand
Here's how IR is used in Quality Control Analyst jobs:
  • Assisted in the execution of the water for injection performance qualification, the HVAC Operational Qualification and the compressed air performance qualification
  • Requested applicant's contact for completion of required documentation for funding eligibility or compliance of guidelines for prior funding received.
  • Conduct analysis of written procedures and submit procedural changes as needed to meet corporate, divisional and/or regulatory requirements.
  • Established an environmental program for a new facility which consisted of several controlled areas and various water systems.
  • Performed various limited software and hardware Network Configurations of Linux and Windows based Servers and test environment setup.
  • Demonstrated proficiency in accessing multiple systems, platforms, application, and data repositories in various data environments.
  • Performed Routine Environmental Monitoring of clean suites, during critical manufacturing operations, and areas under action notice.
  • Assured all internal and external sampling requirements were executed and delivered to meet site and company requirements.
  • Reviewed broker price option reports and verified agents followed strict quality control requirements of the financial institutions.
  • Maintained current knowledge of state and federal regulatory requirements relating to motor vehicle retail installment loan documentation.
  • Work independently and partner with other investigators in various experiments requiring QC studies and specifications release tests.
  • Audited applications for accuracy of information required by state and federal guidelines for program eligibility for funding.
  • Process Subpoena request including reviewing the policy file and providing the required documents which requires investigative abilities.
  • Validated that given test cases stressed specifications in the Business Requirement Document and the Functional Design Document.
  • Review requirements & specifications to perform functional analysis of new application features and/or modifications to be implemented.
  • Involved in discussions in reference to requirements and solutions specifications to better understand the application.
  • Prepared validation summary reports as required including statistical analysis and experimental design for method transfer.
  • Provided accurate chemical level testing of air quality at numerous development sites including DFT measurements.
  • Work closely with Director of Process Improvement, providing unique and exceptional mentoring opportunity.
  • Pay Out responsibilities include reviewing participant requests for contract setup of annual retirement benefits.

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41. Karl Fischer

low Demand
Here's how Karl Fischer is used in Quality Control Analyst jobs:
  • Performed Water Content Determination by Karl Fischer.
  • Performed a wide variety of wet chemical procedures including Karl Fischer, viscosity, specific gravity, and pH determination.
  • Water content analysis of pharmaceutical tablets using Karl Fischer titrations.
  • Perform Karl Fischer analysis and Friability testing on in-process tablets.
  • Wet Chemistry Testing Experience: Determination of moisture content Karl Fischer Testing experience.
  • Conducted moisture analysis by Karl Fischer Analysis and recorded and documented findings.

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42. Data Analysis

low Demand
Here's how Data Analysis is used in Quality Control Analyst jobs:
  • Completed research and development of in-house testing, validation, data analysis, documentation, and environmental monitoring before deadlines.
  • Proposed root cause verification algorithms for unlabeled data analysis, comparing the detection performance with Mahalanobis-Taguchi System.
  • Perform Multivariate data analysis on very large data sets to establish correlations and enhance process understanding.
  • Performed data analysis of product tested and review of manufacturing documents for in-house products.
  • Presented data analysis to senior scientists and senior management at weekly meetings.
  • Performed routine data analysis, investigated OOS results and wrote investigation reports.
  • Performed stability data analysis using statistical software and generated stability reports.
  • Compiled testing data and performed data analysis for annual product reviews.
  • Performed data analysis and management responsibilities for in-house CLIA certified CRO.
  • Developed user friendly data sheets and data analysis excel documents.
  • Excelled at trouble-shooting, investigating unexpected results and data analysis.
  • Performed data entry and data analysis using proprietary statistical software.
  • Inspected and released quarantined materials and conducted data analysis.
  • Executed experimental protocols to include data analysis.
  • Prepared data analysis reports and protocols.
  • Maintained equipment, prepared standards and controls, and other routine work that was needed for timely and successful data analysis.
  • Supported Managers, Directors and VP's by engaging in Data analysis by exporting data from various environments into Excel.
  • Use lean, problem solving methods, and data analysis tools and techniques in validation efforts.
  • Review and develop Drug Product (DP) data analysis techniques using multiple software tools.
  • Conducted data analysis of testing results, review data for SOP compliance and product specifications.

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43. SQL

low Demand
Here's how SQL is used in Quality Control Analyst jobs:
  • Review and validate settlement distribution calculations and entitlement activities in SQL databases.
  • Perform SQL queries using Toad for Oracle to verify and validate data in PROD, UAT, SIT and VAL environments.
  • Use DB2, Oracle, and MSQL databases to develop and maintain test setup and data based on the Business Requirements.
  • Test and produce time series data to check consistency of financial data, filters, and factors using SQL queries.
  • Generated SQL DDL and DML for Software Developers by converting data between: MySQL, MSSQL, and DB2 UDB.
  • Identify if a process needs to be corrected using SQL and other databases Provide Quality Assurance reviews for foreclosed loans.
  • Developed SQL scripts to aid customers in populating tables in the database as well as fix problems with data.
  • Involved in Back-End testing by writing SQL Queries for validating user information in excel sheets and tables.
  • Used SQL queries to extract data from databases and also to verify application front end input value.
  • Used SQL, to run scripts and extract data from the database for data validation of application.
  • Created and maintained monthly SQL queries to check for recurring errors in our data and fixed them.
  • Executed testing automatically using SQL Server agent or manually if SQL Server agent was not available.
  • Experience using MS SQL, HTML to help validate, verify and communicate software issues.
  • Conducted data driven tests on target PowerBuilder, DB2, Oracle, and MSQL databases.
  • Developed SQL scripts to create and update database tables for changes in the database schema.
  • Conducted the database testing of the application by writing SQL Queries using SQL Navigator.
  • Developed a tracking application for quality audits using Access, SQL, and VBA.
  • Run SQL reports and input major info into the Oracle system.
  • Assist the DB team to analyze and optimize SQL queries.
  • Prepared SQL scripts based on Source to target mapping document.

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44. Sds-Page

low Demand
Here's how Sds-Page is used in Quality Control Analyst jobs:
  • Performed SDS-PAGE, scanning, and reports for manufacturing quality release.
  • Experience with protein assays including; SEC, IEC, peptide mapping, aggregation, SDS-PAGE, oxidation
  • Executed Validation for SDS-PAGE, Western Blotting and cIEF.
  • Total Protein Concentrations SDS-Page Chemistry Panels using Hitachi 911 series
  • Developed an SDS-PAGE method for concentration, purity and percent associated of the imbedded targeting arm of a nanoliposomal drug.
  • Oversee daily protein analyses including gel electrophoresis, SDS-Pages, Silver Staining, biorads, Western Blots, and ELISAs.
  • Perform standard panel of assays on products for retail.-qPCR, SDS-PAGE, Endo/exonuclease contamination and unit characterization assays.

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45. Special Projects

low Demand
Here's how Special Projects is used in Quality Control Analyst jobs:
  • Participated in special projects, including new implementation of departmental systems, various remediation projects, and facilitated departmental training classes.
  • Participated in multiple special projects and senior management requests simultaneously associated with safety compliance.
  • Managed special projects with other departments to facilitate and support process improvement.
  • Executed special projects assigned by corporate and quality management staff.
  • Performed, more advanced duties and other special projects such as inventory of samples, archiving of QC documents etc.
  • Be part of some special projects, investigations, assessments and method transfers related to the laboratory and outside laboratories.
  • Complete all testing, including special projects, protocol testing and routine testing in a timely and appropriate manner.
  • Maintained departmental production goals to include random, statistical, stratified, targeted reviews and special projects.
  • Initiated special projects / protocol testing that involves new methods and instrumentation and oversee testing activities.
  • Served as team member in completion of routine functions, validation, and special projects.
  • Assigned merchant account numbers, assisted with new hire training and with special projects.
  • Researched problems in AMS and Export data, work on special projects as required.
  • Handled corporate complaints, special projects and audited outsourced recorded calls as well.
  • Work on special projects / protocol testing that involves new methods and instrumentation.
  • Participate in special projects as directed by Team Leader or Sr. QC Analyst.
  • Revised and updated SOP's and performed test analyses on special projects.
  • Worked on special projects as directed by the Risk Management Department.
  • Completed special projects and other reimbursement related tasks as needed.
  • Assist fellow employees with any special projects or assistance needed.
  • Complete reports and special projects regarding monitoring trends.

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46. Corrective Action

low Demand
Here's how Corrective Action is used in Quality Control Analyst jobs:
  • Performed testing, examined incidences of bugs, facilitated investigations, and managed implementation of corrective action to resolve software glitches.
  • Author deviation investigations and perform root cause analysis per company protocol and determine the proper corrective action as necessary.
  • Initiated deviations, performed investigation on Devotions and Environmental Excursions, and worked on Corrective Actions for Environmental Excursions.
  • Participate in root cause analysis and corrective action identification for deviation occurrences, and properly document investigations.
  • Collaborated with the Quality Assurance department to identify process discrepancy root causes and implemented effective corrective actions.
  • Saved resource costs and eliminated unnecessary overtime through development of root cause analysis and corrective action plans.
  • Key individual for the investigation of Environmental Case Action Reports and corresponding corrective actions via Athena utilization.
  • Reported and documented laboratory test data and out of specification results and implemented corrective action.
  • Performed low and medium level Corrective Action / Preventative Action investigations for laboratory-related non-conformance events.
  • Perform investigations and prepare reports for out-of-specification and failure results and recommend corrective actions.
  • Prepare and reports findings/discrepancies and recommends corrective actions for control and operational improvements.
  • Participate in out-of-specification investigations and provide root cause analysis and corrective actions.
  • Prepared inspection reports that listed all findings and monitored corrective actions.
  • Prepared Quality System reports, including corrective actions and Quality Incidents
  • Reported out-of specification finished products and recommended corrective actions.
  • Identified necessary corrective actions warranted based on audit results.
  • Identified deficiencies and recommended improvements and/or corrective actions.
  • Identify discrepancy and apply disposition and corrective action.
  • Identified quality problems and recommended corrective actions.
  • Recommend appropriate corrective actions as needed.

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47. Product Release

low Demand
Here's how Product Release is used in Quality Control Analyst jobs:
  • Coordinated data entry into TQM database for product specification management and product release.
  • Finalize Certificate of Analysis for product release.
  • Have conducted routine analysis of test samples, raw materials according to standard protocols and methods for product release and validation.
  • Validated biological activity in growth medium supplements by conducting cloning, fusion, ELISA and bone marrow assays before product release.
  • Maintained sample log, Certificate of Analysis documentation, product release files, and Out of Trend/Out of Specification investigations.
  • Performed finished product release testing of liquid, gel, suspension, ointment and solid dosage forms.
  • Report writing, data base entries using SAP R-3 for product release to customers.
  • Tested raw material, in-process, and finished good samples for product release.
  • Perform quality control functions including product release testing and support of stability studies.
  • Ensured standards met in all batch tests and laboratory reports for product release.
  • Analyze in process and finished product clinical chemistry diagnostic samples for product release.
  • Implemented new program for in-house molecular biology assays for drug product release.
  • Batch record review along with data entry and product release.
  • Issued change controls and deviations for product release.
  • Followed process of product release through SAP documentation.
  • Perform product release testing in ELISA assays.
  • Performed Peer Review and Product Release.
  • Interpret test results and Certificates of Analysis (COAs), compare them to established specifications, and initiate product release.
  • Performed Growth Promotion Qualification assay (GPQ) under cGMPs to support product release.
  • Followed approve SOPs for biochemistry assay for product release.

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48. Loan Applications

low Demand
Here's how Loan Applications is used in Quality Control Analyst jobs:
  • Worked with various internal and external resources to verify information taken from loan applications.
  • Reviewed loan applications from borrowers to identify possible fraud.
  • Conduct periodic reviews of approved and declined SC HELP mortgage loan applications for compliance with program requirements and indications of fraud.
  • Review Denied/Withdrawn loan applications for compliance with ECOA.
  • Analyze data and home loan applications.

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49. Trackwise

low Demand
Here's how Trackwise is used in Quality Control Analyst jobs:
  • Write deviations for samples that exceed alert and action limits using TrackWise.
  • Certified investigator responsible for initiating non-conformance investigations via Trackwise; writing out-of-specification and calibration exception reports.
  • Process deviation and Out of Specification (OOS) to document failure and investigation for unexpected test results in Trackwise.
  • Evaluated data results to determine excursion: Alert or Action level ( initiated NCR using TrackWise 8).
  • Use Trackwise to complete the deviation investigation.
  • Initiate all new Evaluations in the Trackwise 8 system and push to the responsible product quality or manufacturing representative.
  • Perform and write Trackwise investigations for OOS results, assay failures, and deviations from SOPs.
  • Initiate Events and initial investigations thru Trackwise 8.

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50. Fannie MAE

low Demand
Here's how Fannie MAE is used in Quality Control Analyst jobs:
  • Assure that Uniform Appraisal Data (UAD) - Fannie Mae Guidelines are met by each UAD Compliant Appraisal Report.
  • Developed claims for reimbursement according to Freddie Mac and Fannie Mae guidelines on behalf of the Client (GMAC).
  • Review servicing systems to ensure compliance with servicing HUD, VA, Fannie Mae, Freddie Mac and portfolio Guidelines.
  • Executed test scripts to ensure governmental guideline compliance for Freddie Mac and Fannie Mae loans.
  • Sound knowledge of the secondary mortgage industry guidelines including Fannie Mae and Freddie Mac.
  • Clear to close residential Fannie Mae or Freddie Mac mortgage loan files.
  • Have knowledge of regulatory boards not USPAP certified, Fannie Mae.
  • Researched and compiled necessary documents for monthly Fannie Mae auditing.
  • Maintain great knowledge of Fannie Mae and Freddie Mac guidelines.
  • Created A Fannie Mae Custody Audit Procedure Booklet.
  • Promoted to quality control Fannie Mae claims.
  • Completed a random sample of Mortgage loan files for a pre-funding audit to comply with Fannie Mae guidelines.
  • Review all quality control reports from outside agencies, such as Fannie Mae and other GSE/NON GSE files.
  • Contract Assignment) Examined loan documentation for adherence to Fannie Mae and Freddie Mac guidelines.
  • Directed workflow to and from offshore team for conventional claims to Fannie Mae.

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20 Most Common Skill for a Quality Control Analyst

Lab Equipment13.7%
Test Procedures10.9%
Ensure Compliance9.3%
Raw Materials8.2%
Analytical Methods7.4%
QC6.3%
Stability Samples5.9%
Hplc5.3%

Typical Skill-Sets Required For A Quality Control Analyst

RankSkillPercentage of ResumesPercentage
1
1
Lab Equipment
Lab Equipment
10.5%
10.5%
2
2
Test Procedures
Test Procedures
8.4%
8.4%
3
3
Ensure Compliance
Ensure Compliance
7.2%
7.2%
4
4
Raw Materials
Raw Materials
6.3%
6.3%
5
5
Analytical Methods
Analytical Methods
5.7%
5.7%
6
6
QC
QC
4.9%
4.9%
7
7
Stability Samples
Stability Samples
4.5%
4.5%
8
8
Hplc
Hplc
4.1%
4.1%
9
9
Test Cases
Test Cases
3.6%
3.6%
10
10
PH Meter
PH Meter
2.9%
2.9%
11
11
Audit Procedures
Audit Procedures
2.7%
2.7%
12
12
Uv/Vis
Uv/Vis
2.6%
2.6%
13
13
Cgmp Regulations
Cgmp Regulations
2.3%
2.3%
14
14
FDA
FDA
2%
2%
15
15
Lims
Lims
1.9%
1.9%
16
16
GC
GC
1.9%
1.9%
17
17
Bioburden
Bioburden
1.6%
1.6%
18
18
Final Product
Final Product
1.4%
1.4%
19
19
Endotoxin
Endotoxin
1.4%
1.4%
20
20
Data Entry
Data Entry
1.4%
1.4%
21
21
Validation Protocols
Validation Protocols
1.3%
1.3%
22
22
ISO
ISO
1.2%
1.2%
23
23
Ftir
Ftir
1.1%
1.1%
24
24
Chromatography
Chromatography
1.1%
1.1%
25
25
QA
QA
1.1%
1.1%
26
26
Microbiology
Microbiology
1.1%
1.1%
27
27
Customer Service
Customer Service
1.1%
1.1%
28
28
Elisa
Elisa
1%
1%
29
29
Wet Chemistry
Wet Chemistry
1%
1%
30
30
GLP
GLP
0.9%
0.9%
31
31
Capa
Capa
0.9%
0.9%
32
32
Preventative Maintenance
Preventative Maintenance
0.8%
0.8%
33
33
R
R
0.7%
0.7%
34
34
LAL
LAL
0.7%
0.7%
35
35
OOS
OOS
0.7%
0.7%
36
36
FHA
FHA
0.7%
0.7%
37
37
Growth Promotion
Growth Promotion
0.6%
0.6%
38
38
Ensure Accuracy
Ensure Accuracy
0.6%
0.6%
39
39
Quality Standards
Quality Standards
0.6%
0.6%
40
40
IR
IR
0.6%
0.6%
41
41
Karl Fischer
Karl Fischer
0.6%
0.6%
42
42
Data Analysis
Data Analysis
0.6%
0.6%
43
43
SQL
SQL
0.6%
0.6%
44
44
Sds-Page
Sds-Page
0.5%
0.5%
45
45
Special Projects
Special Projects
0.5%
0.5%
46
46
Corrective Action
Corrective Action
0.5%
0.5%
47
47
Product Release
Product Release
0.5%
0.5%
48
48
Loan Applications
Loan Applications
0.5%
0.5%
49
49
Trackwise
Trackwise
0.5%
0.5%
50
50
Fannie MAE
Fannie MAE
0.5%
0.5%

29,132 Quality Control Analyst Jobs

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