A QA Associate ensures that the new product in the development meets standards for usage and operations. While actual duties tend to vary, the following are certain core tasks listed on the QA Associate Resume – working with the organization members to audit, identify quality problems, and to improve operational processes; writing, maintaining and disseminating quality complaints, tracking down components, recommending corrective actions, verifying logs, databases, and other data to track and flag quality concerns and improvements.
Employers prefer to hire those possessing the following qualities – strong industry or product knowledge, excellent verbal and written communication skills, the ability to analyze and check for accuracies, and familiarity with the quality processes, and regulations. While the education requirements vary from employer to employer, a degree directly relating to the field of work is needed.
Headline : An ambitious, enthusiastic, and sincere QA Associate with 2 years of QA Testing experience in Manual Testing and some automation testing and 2 years of Java development experience and some knowledge of .NET want to prove myself and my employer with my maximum efforts. Good knowledge and experience in developing and managing all phases of Software Testing Lifecycle (STLC) under SDLC methodologies like Waterfall and Agile.
Skills : QC, QTP, Bugzilla, JIRA, ALM, Selenium, SoapUI, LoadRunner, Oracle 11G, SQL /PL SQL, Oracle, MS SQLServer, Unix, Informatica, Informatica Power Center 9.x.
Description :
Performed system, unit, acceptance, regression, load and functional/performance testing on dozens of applications using both automated and manual testing methods.
Leveraged knowledge of object-oriented programming to help validate, verify, communicate and resolve software issues through careful, thoroughly documented testing to maximize return on investment (ROI) for IT initiatives.
Analyzed the Business Requirements, Functional Specifications and Design Documents with Business Analyst.
Involved in Preparing Test Scenarios, Test Conditions and Test Cases based on the functional specifications, Design Documents and Use Cases.
Involved in Reviewing and Finalizing the Test Cases for the Execution.
Wrote the test scripts in recorded and non-recorded mode both.
Executed the Automated and Manual Test Cases and reviewed the defects.
Experience
5-7 Years
Level
Executive
Education
Master's
QA Associate Resume
Objective : QA Associate with 3 years of experience in Performing testing and related work in the Product Analytical and Bioassay Testing (PABT) organization on in-process, drug substance, and drug products for release or stability programs, Performing laboratory testing in a cGMP environment, and understand the science and compliance needs of the business.
Skills : Inventory Control, Microsoft Suites, QA, and phlebotomy.
Description :
Supported during FDA and other regulatory inspections, and customer audits.
Supported facility regulatory and quality systems and fallowing quality management system.
Supported the CAPA system.
Maintained databases for deviation, OOSs, irregularities and changed control (CC).
Reviewed and approved equipment qualification (IQ/OQ/PQ), process and cleaning validations, reviewed and approved validation documents, quality reports, protocols, final reports and miscellaneous project documentation.
Reviewed and approved material specification, validate Quality Control (QC) spreadsheets, and validate documents ( analytical methods, and cleaning documents).
Reviewed raw materials, analytical and manufacturing documents (Batch Records) related to GMP production including SOPs.
Experience
2-5 Years
Level
Junior
Education
MS
QA Associate Resume
Summary : Over 10 Years Planning Large Conferences for: Teachers, Para-Educators, Chemists, Administrative Staff, and Information Technology Recruiting Fairs Over 25 Years in Administrative Skills including but not limited to: Scheduling Travel, Payroll, Invoices, Budget Management, Grants, Quality Assurance Administration, Typing of Standard Operating Procedures, conducting Telephone Interviews, Scheduling New Hire Training and Processes, Conducting Training Classes, Managed and processed new contractor agreements and rate negotiations, Website updates and other duties as needed.
Entered data and perform tracking and status of Deviations, Corrective Action Plan Action (CAPA), Problem Notifications (PN), etc.) Process existing and new equipment calibration labels for production and laboratory equipment per the approved calibration software program, CalMan.
Assigned equipment numbers to new equipment and enter data into the calibration database.
Entered data for calibrations/equipment qualifications and maintain all calibration records associated with the validated calibration program.
Generated reminder notices for calibration records associated with the validated calibration program.
Generated reminder notices for calibrations due and follow-up until completed.
Created and/or made changes to forms in CalMan.
Wrote revise, reviewed Standard Operating Procedures (SOPs) to control critical processes and assure conformance to Good Manufacturing Practices (GMPs).
Experience
10+ Years
Level
Senior
Education
AA In Business
QA Associate Resume
Summary : As a QA Associate, responsible for Performing a broad variety of basic and moderately complex tests in support of lab operations, performing testing of a routine and non-routine samples and documents according to cGMPs
Skills : Microsoft Office, Educated In Troubleshooting / Maintaining Cisco Routers And Switches, Educated In Troubleshooting Networks And Cisco Equipment, Educated In Networking Protocols, Maintenance And Installation.
Description :
Verified of orderfillers to confirm stores get what they require.
Verified slots for orderfillers to be able to get what they need.
Multi-tasked routinely to provide management and each position with any information or assistance they need.
Trained all new associates to our department in comprehensive policy and procedure.
Generated Certificates of Analysis based on laboratory test results for customers of Paddock Laboratories, Inc.
Monitored the Company's Change Control System for compliance and documentation.
Released Active Pharmaceutical Ingredients (API) for distribution.
Experience
10+ Years
Level
Senior
Education
AA In Networking Specialist
QA Associate Resume
Objective : Results-oriented QA Associate professional with over 7 years of experience in Information Technolo- gy with emphasis on Quality Assurance and Systems Validation. Highly motivated self-starter with ability to work independently and collaboratively within a diverse technical team. Excellent interpersonal communication skills both written and verbal. Strong analytical and problem-solving skills.
Skills : Microsoft Office, Management, Process Improvement, Multi-Tasking, Data Entry, Research.
Description :
Created and executed of quality management plan, test plan and code review process docu- ment.
Fully involved in analyzing business requirement documents and writing master test plan.
Identified and implemented of the testing framework, environment, approach, and methodologies.
Involved in project planning, coordination and implementation of QA methodology.
Involved in automation of test suites for web-based applications.
Responsible for hiring new resources for the QA team formation.
Maintained an exclusive report that includes test metrics and status reports.
Experience
2-5 Years
Level
Executive
Education
GED
QA Associate Resume
Headline : To obtain a responsible, growth-oriented position that would fit my knowledge and skills in which my experience and learning abilities can be fully utilized.
Skills : High Attention To Details, Great Problem Solving, Excellent Customer.
Description :
Assisted in the maintenance of GLP compliance program which includes maintaining master schedule, maintaining copies of protocol pertaining to regulated clinical & non-clinical studies, inspection of critical phases for compliance to assure the integrity of the study.
Reviewed & revised QAU SOP's, review of Laboratory SOP's for quality & compliance objective.
Reviewed final bioanalytical data & final reports to assure the reported results accurately reflect the raw data.
Responsible for the coordination with the project managers to ensure proper QC review of all data tables & reports according to the GLP compliance standards.
Oversaw QC associates, set priorities to facilitate the production of specialized data products according to client specific reporting needs & guidelines.
Maintained laboratory instruments troubleshoot method performance & efficiency problems as they arise.
Managed Quality Control and Sample Control departments.
Experience
5-7 Years
Level
Executive
Education
Diploma
QA Associate Resume
Headline : Responsible for identifying and recommending solutions to potential procedural/process system gaps, Receiving and providing training, and also Participating in assay transfer and assay validation.
Skills : Customer Service, Call Center, Computer Hardware, Troubleshooting, Windows 7.
Description :
In charged of printing and arranging Quality control batch records for distribution to Analysts for testing in the Quality Assurance Department.
Responsible for filing test worksheets into proper batch records and compiling and organizing these completed documents.
Notified Analysts and Validators of pending tests on QC batch records.
Ensured that approved batch records were logged in and transferred to storage.
Filed OOS Reports and maintained this binder.
Entered test results into batch records on the Q-DIS data management system.
Entered information into Q-DIS necessary for bringing records to completion status.
Experience
5-7 Years
Level
Executive
Education
MS
QA Associate Resume
Summary : Responsible for Coordinating with customers to support operational activities, Maintaining a state of inspection readiness, and also Actively participating in group and project teamwork; project and process improvements.
Skills : Microsoft Office Software, 90+ WPM.
Description :
Reviewed of dossier for ASEAN countries following ACTD requirements.
Reviewed of the quality and analytical data as per the pharmacopoeia, specification, MOA, Batch records, Stability and Finished product/ Packaging material data for the purpose of compilation of dossier.
Reviewed and compared labeling documents for the clients including package inserts, reviewing graphics and container/carton labels for FDA compliance with the current understanding and expectations of the authority reviewers.
Reviewed of documents required for regulatory agencies.
Followed up with designer for artwork correction.
Reviewed and approved of previous SOPs based on relevant standards and policies.
Assisted in the validation of QC tests in the Q-DIS data management system.
Experience
7-10 Years
Level
Management
Education
BA
QA Associate Resume
Headline : To apply my knowledge of science, Roche /Genentech products, and hands-on customer/patient experience for the benefit of human life through medicine, education, and the ever-evolving pharmaceutical and research industries.
Skills : VIDAS, GDS, PCR-BAX, MALDI, GC, NMR, IR, Analytical chemistry research of Alzheimer's disease.
Description :
Followed company policies and procedures.
Received specific instruction and work independently to complete tasks.
Met assigned targets and timelines with minimal supervision, and independently prioritizing multiple assigned tasks.
Supported the Product Complaints department and support groups by providing timely, clear, and concise communication.
Created department reports, routine and upon request (e.g. APR data reports, monthly complaint reports).
Communicated with pharmacies and patients to obtain necessary information for complaint investigation.
Demonstrated excellent customer service skills through timely follow up with customers and resolving calls in a timely manner.
Experience
5-7 Years
Level
Executive
Education
Bachelor Of Science
QA Associate Resume
Objective : Experienced in making a positive first impression about myself and the organization. Making customers glad to be a customer, and glad they called. I have Quality Control experience and Document Control experience. Excellent computer skills, and excellent written and verbal communication skills.
Skills : Microsoft Word Advanced, Microsoft Excel Advanced, HACCP Food Safety, Typing 60wpm 100% Accuracy, Quality Control Food Plant, Written & Verbal Communication.
Description :
Placed requests for required Regulatory documents, primarily via email.
Followed up on request for required Regulatory documents, primarily via email.
Reviewed Regulatory documents for correctness and completeness.
Analyzed documents, and brought to attention for correction nutritional statements, and other data needing updating.
Corrected Allergies in products helps save consumers and the company.
Facilitated product complaint sample retrieval and maintain sample inventor according to established procedures, including sample destruction.
Maintained the Product Complaint Laboratory according to established procedures and Genentech Safety, Health and Environmental (SHE).
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